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ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½106¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . phanginin G C21H28O5 ÏàËÆ¶È:66.6% Phytochemistry 2008 69 1242-1249 Phanginin A¨CK, diterpenoids from the seeds of Caesalpinia sappan Linn. Orapun Yodsaoue,Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, Hoong-Kun Fun,Akkharawit Kanjana-Opas Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . phanginin G C21H28O5 ÏàËÆ¶È:66.6% Chinese Journal of Natural Medicines 2012 10 218-221 Two new cassane diterpenoids from the seeds of Caesalpinia sappan Linn. Jing-Yu ZHANG, Fei-Hua WU, Wei QU, Jing-Yu LIANG Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . phanginin P C21H28O5 ÏàËÆ¶È:66.6% Phytochemistry Letters 2014 8 141-144 Three new cassane diterpenes from the seeds of Caesalpinia sappan Guo-Xu Ma, Yin-Di Zhu, Zhong-Hao Sun, Jing-Quan Yuan, Yong Xie, Xiao-Po Zhang, Yu Tian, Jun-Shan Yang, Hai-Feng Wu, Xu-Dong Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . phanginin H C21H28O4 ÏàËÆ¶È:62.5% Phytochemistry 2008 69 1242-1249 Phanginin A¨CK, diterpenoids from the seeds of Caesalpinia sappan Linn. Orapun Yodsaoue,Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, Hoong-Kun Fun,Akkharawit Kanjana-Opas Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3¦Â-methylandrost-5-en-7,17-dione C20H28O2 ÏàËÆ¶È:54.1% Steroids 2010 75 859-869 Stereoselective synthesis of some methyl-substituted steroid hormones and their in vitro cytotoxic activity against human gastric cancer cell line MGC-803 Chun Li, Wenwei Qiu, Zhengfeng Yang, Jian Luo, Fan Yang, Mingyao Liu, Juan Xie, Jie Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . kirinine B C22H31NO3 ÏàËÆ¶È:54.1% Phytochemistry 1998 49 2557-2559 Diterpene alkaloids from Aconitum kirinense Feng Feng, Jing-Han Liu, Shou-Xun Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3¦Â,7¦Â-dihydroxyandrost-5-en-17-one ÏàËÆ¶È:54.1% Phytochemistry 1998 49 2355-2358 The hydroxylation of ¦¤5-androstenes by Cephalosporium aphidicola Caroline M. Bensasson, James R. Hanson, A. Christy Hunter Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Dehydrocardiopetaline ÏàËÆ¶È:54.1% Phytochemistry 1993 34 553-558 Three diterpenoid alkaloids from Delphinium cossonianum Gabriel de la Fuente, Jose A. Gavin, Rafael D. Acosta, Francisco Sanchez-Ferrando Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 20¦Á-Acetylamino-11¦Á-hydroxy-5¦Á-pregnan-3-on ÏàËÆ¶È:54.1% Steroids 1998 63 484-495 Microbial hydroxylation of acetylaminosteroids HerbertL Holland, Gingipalli Lakshmaiah, PeterL Ruddock Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . phanginin M C21H24O6 ÏàËÆ¶È:54.1% Chinese Journal of Natural Medicines 2012 10 218-221 Two new cassane diterpenoids from the seeds of Caesalpinia sappan Linn. Jing-Yu ZHANG, Fei-Hua WU, Wei QU, Jing-Yu LIANG Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 11a C24H38O7 ÏàËÆ¶È:54.1% Heterocycles 2000 53 599-612 Hydrogenation Derivatives of Neo-clerodanes and Their Antifeedant Activity Maurizio Bruno, Sergio Rosselli, Ivana Pibiri, Franco Piozzi,* and Monique S. J. Simmonds Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . daphcalycine C23H33NO3 ÏàËÆ¶È:54.1% The Journal of Organic Chemistry 2003 68 300-304 Daphcalycine, a Novel Heptacycle Fused Ring System Alkaloid from Daphniphyllum calycinum Akino Jossang, Hoda El Bitar, Van Cuong Pham, and Thierry S¨¦venet Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . dehydronapelline ÏàËÆ¶È:54.1% Pharmaceutical Biology 2006 44 244-246 Alkaloids from Consolida olopetala. L. Bitiş, S. S¨¹zgeç, F. Meriçli, H. Özçelik, J. Zapp, H. Becker, A.H. Meriçli Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . dehydronapelline C22H31NO3 ÏàËÆ¶È:54.1% Heterocycles 1987 26 1455-1460 Studies on the Active Principles from Aconitum flavum Hand-Mazz. The Structures of Five New Deterpenoid Alkaloids Zhi-gang Chen, Ai-na Lao, Hong-chemg Wang, and Shan-hai Hong Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . dehydrolucidusculiine C24H33NO4 ÏàËÆ¶È:54.1% Heterocycles 1985 23 2473-2477 Two New C20-Diterpenoid Alkaloids from Aconitum yesoense var. macroyesoense (Nakai) Tamura, Structures of Dehydrolucidusculine and N-Deethyldehydrolucidusculine Koji Wada, Hideo Bando, and Takashi Amiya Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . calycilactone A C22H29NO3 ÏàËÆ¶È:54.1% Tetrahedron Letters 2006 47 5329-5331 Calycilactone A, a novel hexacyclic alkaloid from Daphniphyllum calycillum Ying-Tong Di, Hong-Ping He, Hai-Yang Liu, Zhi-Zhi Du, Jun-Mian Tian, Xian-Wen Yang, Yue-Hu Wang, Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 12¦Â,24(R)-dihydroxy-3-oxo-cycloart-1,25(26)-dien-21-oic acid ÏàËÆ¶È:53.5% Phytochemistry 1998 49 2069-2076 Cycloartenoid dienone acids and lactones from Combretum erythrophyllum Colin B. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 10 C25H34O6 ÏàËÆ¶È:52% Bioorganic & Medicinal Chemistry 2011 19 2450-2457 Synthesis of rabdokunmin C analogues and their inhibitory effect on NF-§ÜB activation Yutaka Aoyagi,Yoshiyuki Adachi, Kei Ozawa ,Chihiro Yokomizo ,Ming-Yu Gui , Yong-Ri Jin,Xu-Wen Li, Naohito Ohno , Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 15-hydroxy-ent-beyer-15-en-succinate methyl ester C25H38O4 ÏàËÆ¶È:52% Phytochemistry 1989 28 517-526 Sesquiterpene lactones and other constituents from Australian Helipterum species C. Zdero,F. Bohlmann,R.M. King,H. Robinson Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Puqiedine C27H45NO2 ÏàËÆ¶È:51.8% Steroids 2006 71 843-848 New steroidal alkaloids from the bulbs of Fritillaria puqiensis Yan Jiang, Ping Li, Hui-Jun Li, Hua Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . petilidine ÏàËÆ¶È:51.8% Chinese Traditional and Herbal Drugs 2009 40 15-17 Alkaloid constituents of Fritillaria cirrhosa CAO Xin-wei; ZHANG Meng; LI Jun; XIAO Pei-gen; CHEN Si-bao; CHEN Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . puqiedine ÏàËÆ¶È:51.8% Journal of Asian Natural Products Research 2011 13 1098-1103 Steroidal alkaloids from the bulbs of Fritillaria unibracteata Qing-Jian Zhang, Zhong-Fei Zheng & De-Quan Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . cycloart-24-en-3¦Â,26-diol ÏàËÆ¶È:51.8% Chinese Journal of Natural Medicines 2012 10 36-39 Chemical constituents of Allophylus longipes Xiang-Yun ZHANG, Xiang-Hai CAI, Xiao-Dong LUO Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 3¦Â-hydroxy-29-norcycloart-24-one C29H48O2 ÏàËÆ¶È:51.7% Chemical & Pharmaceutical Bulletin 2001 49(2) 183-187 Triterpenes and Lignans from Artemisia caruifolia and Their Cytotoxic Effects on Meth-A and LLC Tumor Cell Lines Chao-mei MA, Norio NAKAMURA, Byung Sun MIN, and Masao HATTORI Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 17¦Â-hydroxy-3,11,16-trioxo-28-norolean-12-ene C29H42O4 ÏàËÆ¶È:51.7% Planta Medica 2003 69 258-264 New Dihydrobenzofurans and Triterpenoids from Roots of Microglossa pyrifolia homas J.Schmidt,Meike R.Hildebrand,G¨¹nter Willuhn Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . griffith ine A C30H50O2, ÏàËÆ¶È:51.7% Acta Botanica Yunnanica 1997 19(3) 321-323 STUDIES ON CHEMICAL CONSTITUENTS FROM LEAVES OF GONIOTHALAMU SGRIFFITH II L i Chaom ing,L iu Zhenglian ,M u Q ing, Sun Handong,Zheng Hu ilan, Tao Guoda Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . lehmannolol C24H32O4 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2006 54(11) 1595-1598 Sesquiterpene Coumarins from the Roots of Ferula sinkiangensis and Ferula teterrima Jun-Rong YANG,Zheng AN,Zhi-Hong LI,Song JING,and Hai-Lin QIN Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . phanginin F C21H26O5 ÏàËÆ¶È:50% Phytochemistry 2008 69 1242-1249 Phanginin A¨CK, diterpenoids from the seeds of Caesalpinia sappan Linn. Orapun Yodsaoue,Sarot Cheenpracha, Chatchanok Karalai, Chanita Ponglimanont,Suchada Chantrapromma, Hoong-Kun Fun,Akkharawit Kanjana-Opas Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . excoecarin D C20H30O3 ÏàËÆ¶È:50% Journal of Natural Products 2000 63 344-346 Excoecarins D, E, and K, from Excoecaria agallocha Tenji Konishi, Takao Konoshima, Yasuhiro Fujiwara, and Shiu Kiyosawa Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (+)-17-oxocycloprotobuxine C23H37NO ÏàËÆ¶È:50% Journal of Natural Products 1999 62 665-669 New Steroidal Alkaloids from the Roots of Buxus sempervirens Atta-ur-Rahman, Athar Ata, Samina Naz, M. Iqbal Choudhary, Bilge Sener, and Songul Turkoz Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 12-epi-dehydronapelline C22H31NO ÏàËÆ¶È:50% Planta Medica 2005 71 1073-1076 Three New Diterpene Alkaloids from the Roots of Aconitum nagarum var.lasiandrum Fan Zhang , Shu-Lin Peng , Xun Liao , Kai-Bai Yu , Li-Sheng Ding Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . ent-beyer-15-en-18-O-succinate C24H36O4 ÏàËÆ¶È:50% Planta Medica 2002 68 361-363 Antibacterial Diterpenoids from Fabiana densa var.ramulosa Silvia Erazo,Mercedes Zald¨ªvar,Carla Delporte,Nadine Backhouse,Paola Tapia,Eliana Belmonte,Franco Delle Monache,Rosa Negrete Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 11-acetyl-l,19-epoxydenudatine C24H33NO4 ÏàËÆ¶È:50% Planta Medica 1990 56 461-463 11 -Acetyl- 1, 19-epoxydenudatine:A New Alkaloid from Aconitum barbatum B. Proksa, D. UhrIn, D. Batsuren, N. Batbaiar, and D. Selenge Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . subdesculine ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1988 36 1604-1606 STRUCTURES OF SECOJESACONITINE AND SUBDESCULINE, TWO NEW DITERPENOID ALKALOIDS FROM ACONITUM JAPONICUM THUNB. Hideo Bando,Koji Wada,Takashi Amiya,Yasuo Fujimoto and Kimiko Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 11-Acetyl-1,19-Epoxydenudatine C24H35NO4 ÏàËÆ¶È:50% Chemistry of Natural Compounds 1992 28 388-389 ALKALOIDS OF THE MONGOLIAN FLORA I. ALKALOIDS OF THE EPIGEAL PART OF Aconitum barbatum N. Batbayar, D. Batsuren, and M. N. Sultankhodzhaev Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 25(R)-4¦Â,5¦Â-Epoxy-6-spirosten-3¦Â-ol ÏàËÆ¶È:50% Molecules 2003 8 886-893 Epoxidation of Diosgenin, 25(R)-1, 4, 6-Spirostatrien-3-one and 25(R)-4, 6-Spirostadien-3¦Â-ol Eunsook Ma and Jongwon Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 3¦Á,7¦Á,12¦Á-Trihydroxy-5¦Â-cholestan-26,27-dioic acid C27H44O7 ÏàËÆ¶È:50% Steroids 2000 65 143-147 A convenient synthesis of 5¦Â-cholestan-26-oic and 5¦Â-cholestan-26,27-dioic acids I. Starchenkov, P. Trapencieris, V. Kauss, G. Jas, I. Kalvinsh Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . (5'R,17S)-5'-ethylspiro[estr-4-ene-3-one-17,2'-tetrahydrofuran-3'-one ÏàËÆ¶È:50% Steroids 2001 66 569-579 Synthesis of C-5¡ä-alkyl substituted 17-spirofuran 19-norsteroids Vladimir A. Khripach, Vladimir N. Zhabinskii, Dmitrii N. Tsavlovskii, Olga A. Drachenova, Galina V. Ivanova, Olga V. Konstantinova, Margarita I. Zavadskaya, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . spiro dienone C24H31O7Cl ÏàËÆ¶È:50% Steroids 2004 69 23-34 Isolation and structure elucidation of the major photodegradation products of loteprednol etabonate Yoshihisa Shirasaki, Katsuhiro Inada, Jun Inoue, Masayuki Nakamura Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . Ethyl 17¦Á-hydroxyandrostane-16¦Á-carboxylate ÏàËÆ¶È:50% Steroids 2004 69 271-277 Selective ring-opening carbonylation of epoxy-steroids Attila Bal¨¢zs, Csilla Benedek, G¨¢bor Szalontai, Szil¨¢rd Tőrös Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . Otostegin B C22H34O6 ÏàËÆ¶È:50% Phytochemistry 2000 54 771-775 Labdane diterpenes from Otostegia fruticosa Nawal M. Al-Musayeib, Fawkeya A. Abbas, M. Shamim Ahmad, Jaber S. Mossa, Farouk S. El-Feraly Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . 2¦Á-hydroxy-3¦Á,5-cycloandrostane-6,17-dione C19H26O3 ÏàËÆ¶È:50% Phytochemistry 1999 52 1279-1282 The microbiological hydroxylation of 3¦Á,5-cycloandrostanes by Cephalosporium aphidicola Caroline S. Bensasson, James R. Hanson, Yvan Le Huerou Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . methyl ent-1¦Â,7¦Á-dihydroxy-16-ketobeyeran-19-oate ÏàËÆ¶È:50% Phytochemistry 1999 51 737-741 Biotransformation of the diperpenoid, isosteviol, by Aspergillus niger, Penicillium chrysogenum and Rhizopus arrhizus Bras H. de Oliveira, Marcia C. dos Santos, Paulo C. Leal Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 11-acetyl-1,19-epoxydenudatine ÏàËÆ¶È:50% Phytochemistry 1998 49 2557-2559 Diterpene alkaloids from Aconitum kirinense Feng Feng, Jing-Han Liu, Shou-Xun Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . jamesoniellide B C22H30O7 ÏàËÆ¶È:50% Journal of Natural Products 1992 Vol 55 111 Ent-Labdanes and Furanoditerpenes from the Liverwort Jamesoniella autumnalis Martin Blechschmidt, Hans Becker Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . compound 9 ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 2170 The Absolute Stereochemistry of Senexdiolic Acid at C-22 Antonio G. Gonz¨¢lez, Teresa Siverio Exp¨®sito, Jaime Bermejo Barrera, Ana Garc¨ªa Castellano, Francisco J. Toledo Marante Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (1R,2R,3R,6S,7S,9R,10R,14R)-3-butanoyloxycladiell-11(17)-en-6,7-diol C24H40O5 ÏàËÆ¶È:50% Journal of Natural Products 1994 Vol 57 574 New Cladiellane Diterpenes from the Soft Coral Cladiella australis of the Andaman and Nicobar Islands C. Bheemasankara Rao, D. Sreenivasa Rao, C. Satyanarayana, D. Venkata Rao, Katharina E. Kass¨¹hlke, D. John Faulkner Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . phlomisoside F C26H36O9 ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 2009 Vol 44 60-62 A new furanolabdane diterpene glycoside from Phlomis younghusbandii Mukerjee ZHAO Bin; LIANG Heng-xing; YU Ya-fang; DONG Xiao-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . Argenteanol C30H50O4 ÏàËÆ¶È:50% Phytochemistry 1996 41 1325-1328 Cytotoxic cycloartanes from aglaia argentea O. R. Omobuwajo, M. -T. Martin, G. Perromat, T. Sevenet, K. Awang, M. Païs Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 16¦Á,17-Isopropylideno-3-oxo-phyllocladane C23H36O3 ÏàËÆ¶È:50% Phytochemistry 1994 37 587-588 16oc, 17-isopropylideno-3-oxo-phyllocladane, a diterpenoid from Callicarpa macrophylla Anil K. Singh, Pawan K. Agpawal Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . Graciline ÏàËÆ¶È:50% Phytochemistry 1993 34 553-558 Three diterpenoid alkaloids from Delphinium cossonianum Gabriel de la Fuente, Jose A. Gavin, Rafael D. Acosta, Francisco Sanchez-Ferrando Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . caesaljapin C21H28O5 ÏàËÆ¶È:50% Phytochemistry 1992 31 2897-2898 Caesaljapin, a cassane diterpenoid from Caesalpinia decapetala var. Japonica Kazunori Ogawa, Izumi Aoki, Yutaka Sashida Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . monomethyl ester of caesaljapin ÏàËÆ¶È:50% Phytochemistry 1992 31 2897-2898 Caesaljapin, a cassane diterpenoid from Caesalpinia decapetala var. Japonica Kazunori Ogawa, Izumi Aoki, Yutaka Sashida Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . venulol diacetyl derivative ÏàËÆ¶È:50% Phytochemistry 1992 31 3239-3241 Two C20 diterpenoid alkaloids from Delphinium venulosum A. Ulubelen, A.H. Mericli, F. Mericli, R. Ilarslan, S.A. Matlin Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . 12-epidehydronapelline C22H31NO3 ÏàËÆ¶È:50% Korean Journal of Pharmacognosy 2008 39(2) 127-134 Isolation and Oxidation Characteristics of Alkaloids of Aconitum volubile Heo, Kyong-Hee; Lee, Chung-Kyu Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . 16-(4-chloro-benzylidene)-5¦Á-androstan-3,17-dione C26H31ClO2 ÏàËÆ¶È:50% Steroids 2011 76 709-723 Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . Mitrephorone B C21H28O4 ÏàËÆ¶È:50% Organic Letters 2005 Vol. 7, No. 25 5709-5712 A Hexacyclic ent-Trachylobane Diterpenoid Possessing an Oxetane Ring from Mitrephora glabra Chen Li, Dongho Lee, Tyler N. Graf, Sharnelle S. Phifer, Yuka Nakanishi,Jason P. Burgess, Soedarsono Riswan, Fransisca M. Setyowati,Achmad M. Saribi, Djaja D. Soejarto, Norman R. Farnsworth,Joseph O. Falkinham III, David J. Kroll, A. Douglas Kinghorn,Mans Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . compound 19 C26H37NO6S ÏàËÆ¶È:50% Organic Letters 2004 Vol. 6, No. 7 1123-1126 Total Synthesis of (¡À)-Kalihinol C Ryan D. White, Gregg F. Keaney, Corin D. Slown, and John L. Wood Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . compound 2b ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2006 54 1370-1379 Studies on Nepalese Crude Drugs. XXIX. Chemical Constituents of Dronapuspi, the Whole Herb of Leucas cephalotes SPRENG. Yukinori Miyaichi, Akiko Segawa and Tsuyoshi Tomimori Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . spiradine A C21H27NO2 ÏàËÆ¶È:50% Phytochemistry 1988 27 3949-3953 Alkaloids of formosan Thalictrum sessile Yang-Chang Wu,Tian-Shung Wu,Masatake Niwa,Sheng-Teh Lu,Yoshimasa Hirata Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . 15,16-dihydroxy-2¦Á-succinyloxy-labda-3,13-diene C20H30O4 ÏàËÆ¶È:50% Phytochemistry 1990 29 2217-2222 Sesqui-and diterpenes from Baccharis species J. Jakupovic,A. Schuster,U. Ganzer,F. Bohlmann,P.E. 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Reactivity difference between 2¦Â-, 6¦Â- and 16¦Â-azido-androstanes Klaudia Feh¨¦r, J¨¢nos Balogh, Zsolt Cs¨®k, Tam¨¢s K¨¦gl, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . 15-Acetylsongoramine ÏàËÆ¶È:50% Molecules 2012 17 5187-5194 Diterpenoid Alkaloids from the Chinese Traditional Herbal ¡°Fuzi¡± and Their Cytotoxic Activity Feng Gao, Yuan-Yuan Li, Dan Wang, Xing Huang and Qian Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 72 . compound 11b C24H38O7 ÏàËÆ¶È:50% Heterocycles 2000 53 599-612 Hydrogenation Derivatives of Neo-clerodanes and Their Antifeedant Activity Maurizio Bruno, Sergio Rosselli, Ivana Pibiri, Franco Piozzi,* and Monique S. J. 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Gonz¨¢lez, Gabriel de la Fuente, Mat¨ªas Reina, and Isabel Tim¨®n Structure 13C NMR ̼Æ×Ä£Äâͼ 79 . sequoiamonascin A C23H28O6 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2003 68 4966-4969 Sequoiamonascins A-D: Novel Anticancer Metabolites Isolated from a Redwood Endophyte Donald B. Stierle, Andrea A. Stierle, and Timothy Bugni Structure 13C NMR ̼Æ×Ä£Äâͼ 80 . mixture of E and Z isomers of N'-1-[(1SR,5SR)-5-methylbicyclo[3.2.0]hep-2-yliden]-4-methyl-1-toluene-sulfonoylhydrazone C15H20O2SN ÏàËÆ¶È:50% The Journal of Organic Chemistry 2000 65 7839-7846 An Asymmetric Synthesis of (+)-Grandisol, a Constituent of the Aggregation Pheromone of the Cotton Boll Weevil, via a Kinetic Resolution David P. G. Hamon and Kellie L. Tuck Structure 13C NMR ̼Æ×Ä£Äâͼ 81 . (1S*,3S*,4R*,7S*,8S*,12S*,13S*)-7-isocyanocycloamphilect-11(20)-ene C21H29N ÏàËÆ¶È:50% The Journal of Organic Chemistry 1996 61 3259-3267 Novel Potent Antimalarial Diterpene Isocyanates, Isothiocyanates, and Isonitriles from the Tropical Marine Sponge Cymbastela hooperi Gabriele M. König and Anthony D. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ 82 . isosuaveolic acid C20H32O3 ÏàËÆ¶È:50% Chemistry & Biodiversity 2013 10 1494-1500 Abietane Diterpenes from Hyptis suaveolens Saowanee Prawatsri, Apichart Suksamrarn, Anon Chindaduang and Thitima Rukachaisirikul Structure 13C NMR ̼Æ×Ä£Äâͼ 83 . ethyl 2-((3R,5R)-5-((6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-3H-3a,6-methanobenzo[c]isothiazole-1-carbonyl)-3-(furan-2-yl)isoxazolidin-2-yl)acetate C22H30N2O7S ÏàËÆ¶È:50% Tetrahedron 2013 69 9381-9390 Stereoselective 1,3-dipolar cycloadditions of nitrones derived from amino acids. Asymmetric synthesis of N-(alkoxycarbonylmethyl)-3-hydroxypyrrolidin-2-ones Original Research Article Pedro Merino, Graziella Greco, Tom¨¢s Tejero, Ramon Hurtado-Guerrero, Rosa Matute, Ugo Chiacchio, Antonino Corsaro, Venerando Pistar¨¤, Roberto Romeo Structure 13C NMR ̼Æ×Ä£Äâͼ 84 . oblongolide L C22H34O5 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2005 2005 4009-4016 New Oblongolides Isolated from the Endophytic Fungus Phomopsis sp. from Melilotus dentata from the Shores of the Baltic Sea Jingqiu Dai, Karsten Krohn, Dietmar Gehle, Ines Kock, Ulrich Flörke, Hans-J¨¹rgen Aust, Siegfried Draeger, Barbara Schulz and Joachim Rheinheimer Structure 13C NMR ̼Æ×Ä£Äâͼ 85 . (-)-(5S,6R,8S,9S,10R,12Z,14R)-6-acetoxycassa-12,15-diene C22H34O2 ÏàËÆ¶È:50% Phytochemistry 2013 96 397-403 Cassane diterpenes from Caesalpinia platyloba Mario A. G¨®mez-Hurtado, Fany E. ¨¢lvarez-Esquivel, Gabriela Rodr¨ªguez-Garc¨ªa, Mauro M. Mart¨ªnez-Pacheco, Rosa M. Espinoza-Madrigal, Teresa Pamatz-Bolaños, Jos¨¦ L. 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XXXIII.* Preparation of 15,16-Dihydroisopimaric Acid and Methyl Dihydroisopimarate and their Transformations Yu. V. Kharitonov, E. E. Shul¡¯ts, M. M. Shakirov Structure 13C NMR ̼Æ×Ä£Äâͼ 89 . methyl 3¦Á-hydroxy-7,12-dioxo-5¦Â-cholanoate ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 1991 29 190-193 13C NMR spectra of multifunctional bile acid derivatives Erich C. Blossey, Warren T. Ford and Mookkan Periyasamy Structure 13C NMR ̼Æ×Ä£Äâͼ 90 . compound 12 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 1986 24 853-861 Substituent effects on carbon-13 chemical shifts and the stereochemistry of ent-beyeranic and ent-beyer-15-enic compounds substituted on the bicyclo[3.2.1]octane moiety A. Garc¨ªa-Granados, A. Mart¨ªnez, M. E. Onorato and J. Santoro Structure 13C NMR ̼Æ×Ä£Äâͼ 91 . 17¦Á-[4-(4-propylphenyl)-1H-1,2,3-triazol-1-yl]-5¦Á-androst-2-ene C30H41N3 ÏàËÆ¶È:50% Steroids 2011 76 1141-1148 Synthesis of novel steroidal 17 -triazolyl derivatives via Cu(I)-catalyzed azide-alkyne cycloaddition, and an evaluation of their cytotoxic activity in vitro ¨¦va Frank∗, Judit Moln¨¢r, Istv¨¢n Zupk¨®, Zal¨¢n K¨¢d¨¢r, J¨¢nos Wölfling Structure 13C NMR ̼Æ×Ä£Äâͼ 92 . 5¦Á-Androstan-12¦Á-ol C18H32O ÏàËÆ¶È:50% Organic Magnetic Resonance 1977 9 439-464 13C n.m.r. spectra of steroids ¡ªa survey and commentary J. W. Blunt and J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 93 . 1-(Cyclobutylmethoxy)domesticine C24H27NO4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 5861-5868 New aporphinoid 5-HT2A and ¦Á1A antagonists via structural manipulations of nantenine Sandeep Chaudhary, Shashikanth Ponnala, Onica LeGendre, Junior A. Gonzales, Hern¨¢n A. Navarro, Wayne W. Harding Structure 13C NMR ̼Æ×Ä£Äâͼ 94 . 13¦Â-hydroxy-3,15-dioxoatis-16-ene C20H28O3 ÏàËÆ¶È:50% Phytochemistry 2012 75 153-158 Diterpenoids from Euphorbia neriifolia Jun-Hua Liu, Abdul Latif, Mumtaz Ali, Gui-Ping Zhang, Wen-Juan Xiang, Lei Ma, Mohammad Arfan, Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 95 . compond 20 C24H35NO5Br ÏàËÆ¶È:50% Tetrahedron 2012 68 5668-5676 New reactivities of deltaline analogs: an efficient O-demethylation at C-1 and an unusual extrusion of the C-14 atom Pei Tang, Qi-Feng Chen, Ling Wang, Qiao-Hong Chen, Xi-Xian Jian, Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 96 . N-[(3S)-3-Phenyl-heptanoyl]bornane-10,2-sultam C23H33NO3S ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2008 56 11367-11375 Chiral ¦Ã-Aryl-1H-1,2,4-triazole Derivatives as Highly Potential Antifungal Agents: Design, Synthesis, Structure, and in Vitro Fungicidal Activities Xiufang Cao, Fei Li, Ming Hu, Wenchang Lu, Guang-Ao Yu and Sheng Hua Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 97 . N-[(3S)-3-(4-Chlorophenyl)heptanoyl]bornane-10,2-sultam C23H32ClNO3S ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2008 56 11367-11375 Chiral ¦Ã-Aryl-1H-1,2,4-triazole Derivatives as Highly Potential Antifungal Agents: Design, Synthesis, Structure, and in Vitro Fungicidal Activities Xiufang Cao, Fei Li, Ming Hu, Wenchang Lu, Guang-Ao Yu and Sheng Hua Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 98 . compound 8l C22H35NO5 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 99 . compound 8z C23H37NO5 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 100 . compound 13q C25H34N2O5 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 101 . compound 13r C28H37N3O5 ÏàËÆ¶È:50% The Journal of Organic Chemistry 2012 77 7435-7470 Assembly of Four Diverse Heterocyclic Libraries Enabled by Prins Cyclization, Au-Catalyzed Enyne Cycloisomerization, and Automated Amide Synthesis Jiayue Cui, David I. Chai, Christopher Miller, Jason Hao, Christopher Thomas, JingQi Wang, Karl A. Scheidt, and Sergey A. Kozmin Structure 13C NMR ̼Æ×Ä£Äâͼ 102 . (2R)-N-[(aS,2S,5S)-Tetrahydro-a,5-dimethyl-5-vinyl-2-furanacetyl]bornane-10,2-sultam C20H31NO4S ÏàËÆ¶È:50% Chemistry & Biodiversity 2013 10 1252-1259 Diastereoselective Synthesis of a Lilac Aldehyde Isomer and Its Electrophysiological Detection by a Moth Marc-Andr¨¦ Schneider, Stefan Dötterl and Karlheinz Seifert Structure 13C NMR ̼Æ×Ä£Äâͼ 103 . (2E)-1-((10R,13S)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3-hydroxy-10,13-dimethyl-1H-cyclopenta[a]phenanthren-17-yl)-3-(4-methoxyphenyl)prop-2-en-1-imine C29H39NO3 ÏàËÆ¶È:50% Steroids 2013 78 945-950 Synthesis antimicrobial and antioxidant studies of new oximes of steroidal chalcones Imtiyaz H. Lone, Khaliquz Z. Khan, Bharat I. Fozdar, Fida Hussain Structure 13C NMR ̼Æ×Ä£Äâͼ 104 . (5¦Á,13¦Á,17¦Á)-16-hydrazono-10,17-dimethylgonan ÏàËÆ¶È:50% Steroids 2013 78 1177-1182 Synthesis of novel 13¦Á-18-nor-16-carboxamido steroids via a palladium-catalyzed aminocarbonylation reaction Eszter Sz¨¢nti-Pint¨¦r, Zsolt Cs¨®k, Zolt¨¢n Berente, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes Structure 13C NMR ̼Æ×Ä£Äâͼ 105 . (5¦Á,13¦Á,17¦Á)-16-(N,N-dibutyl-carboxamido)-10,17-dimethylgon-16-ene C28H47NO ÏàËÆ¶È:50% Steroids 2013 78 1177-1182 Synthesis of novel 13¦Á-18-nor-16-carboxamido steroids via a palladium-catalyzed aminocarbonylation reaction Eszter Sz¨¢nti-Pint¨¦r, Zsolt Cs¨®k, Zolt¨¢n Berente, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes Structure 13C NMR ̼Æ×Ä£Äâͼ 106 . N-[(L)-2,10-camphorsulfonyl]-(1R,3S,5R,7S)-3-fluoro-5-methyladamantane-1-carboxyamide C22H33FO3S ÏàËÆ¶È:50% Tetrahedron 2013 69 10357-10360 Synthesis of optically active fluoroadamantane derivative having different substituents on its tert-carbons and its use as a non-racemizable source for new optically active adamantane derivatives Original Research Article |

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Joshi,James B. Gloer, and Donald T. Wicklow Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5-(di-tert-Butylfluorosilyl)-2,3-dimethoxybenzoic acid C17H27O4FSi ÏàËÆ¶È:54.5% Molecules 2011 16 7458-7479 t-Bu2SiF-Derivatized D2-Receptor Ligands:The First SiFA-Containing Small Molecule Radiotracers for Target-Specific PET-Imaging Ljuba Iovkova-Berends, Carmen Wängler, Thomas Zöller, Georg Höfner, Klaus Theodor Wanner, Christian Rensch, Peter Bartenstein, Alexey Kostikov, Ralf Schirrmacher, Klaus Jurkschat and Björn Wängler Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-cyclohexylamino-4-methyl-6-oxo-1,4,5,6-tetrahydropyridine-3-carbonitrile ÏàËÆ¶È:54.5% Heterocycles 2010 81 329-347 Cyclization of 5-Cyano-6-cyanoimino-3,4-dihydropyridin-2(1H)-ones with Amines N¨²ria Mont, Francisco Carri¨®n, Jos¨¦ I. Borrell, and Jordi Teixid¨® Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Eleutherazine B C22H36N4O6 ÏàËÆ¶È:54.5% Journal of Asian Natural products Research 2010 12 51-55 Two diketopiperazines from Acanthopanax senticosus Harms Zhi-Feng Li; Nan Xu; Bao-Min Feng; Qi-Hui Zhang; Yue-Hu Pei Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . »·(ÁÁ-ò¡)¶þëÄ ÏàËÆ¶È:54.5% Chinese Traditional and Herbal Drugs 2008 39 502-504 ºìÊ÷ÁÖÕæ¾úÅÝÊ¢¾ÆÇúùÖеĻ·¶þëĺͺËÜÕÀà³É·Ö ¸ßê»;ÌÆ½ðɽ;ºé¿û;ׯÁî;ÕÅÖ¾»ª;ÍõÄËÀû;Ò¦ÐÂÉú Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . cyclo(L-Leu-L-Val) ÏàËÆ¶È:54.5% Chinese Journal of Medicinal Chemistry 2010 20 298-303 Secondarymetabolites from marine actinomycete Streptomyces sp. (No. 30701) ZENG Xue-rong, JIAO Wei-hua, TANG Jin-shan, GAO H ao, HONG Kui, LI Jia, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 6¦Á-Chloro-2,2-dimethyl-3¦Á-(pivaloyloxy)methylpenamS,S-dioxide C13H21O5BSCl ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 1995 3 95-100 Synthesis and elastase inhibitory activity of 6¦Á-chloro-2,2-dimethyl-3¦Á-(pivaloyloxy)methylpenam sulfone, 6¦Á-chloro-2,2-dimethyl-3-exo-methylenepenam sulfone, benzyl and methyl 6¦Á-substituted penicillanate sulfones Carlos E. Boschetti, Oreste A. Mascaretti, Julia A. Cricco, Oscar A. Roveri Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 6-Allyl-6-(2-methoxyethyl)-5,6-dihydro-2,4(1H,3H)-pyridinedione C11H16NO3 ÏàËÆ¶È:54.5% European Journal of Organic Chemistry 2012 334-344 A New Method of Synthesis of 6-Substituted Piperidine-2,4-diones from Homoallylamines Nikolai Yu. Kuznetsov, Victor I. Maleev, Victor N. Khrustalev, Anna F. Mkrtchyan, Ivan A. Godovikov, Tatyana V. Strelkova and Yuri N. Bubnov Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (6S)-1-aza-9,9-bis(trifluoromethyl)-8-oxabicyclo[4.3.0]nonane-2,7-dione C9H7NO3F6 ÏàËÆ¶È:54.5% Heterocycles 2003 61 259-269 Hexafluoroacetone as Protecting and Activating Reagent: An Efficient Strategy for Activation of Pyroglutamic Acid and Homologues Ksenia Pumpor, Christoph Böttcher, Susanna Fehn, and Klaus Burger* Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . cyclo-(Leu-Val) C11H20O2N2 ÏàËÆ¶È:54.5% Natural Product Research and Development 2004 16 383-386 CYCLODIPEPTIDES FROM THE ROOTS OF PANAX NOTOGINSENG WANG Shuang-ming;TAN Ning-hua *; YANG Ya-bin; HE Min Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 1H-2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]-azepin-1-ium trifluoromethanesulfonate C10H17F3N2O3S ÏàËÆ¶È:54.5% Russian Journal of Organic Chemistry 2010 46 383-388 Trifluoromethanesulfonate, trifluromethylsulfonylimide, and bis(trifluoromethylsulfonyl)imide salts and ionic liquids based on 1,8-diazabicyclo[5.4.0]undec-7-ene and 1,5-diazabicyclo[ 4.3.0]non-5-ene L. L. Tolstikova, A. V. Bel¡¯skikh and B. A. Shainyan Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . cyclo(L-Leu-L-Val) C11H20N2O2 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2012 20 2002-2009 Cyclic dipeptides exhibit potency for scavenging radicals Tadashi Furukawa, Takashi Akutagawa, Hitomi Funatani, Toshikazu Uchida, Yoshihiro Hotta, Masatake Niwa, Yoshiaki Takaya Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-chloro-5-isopropyl-3-oxocyclohex-1-enyl methyl carbonate C11H15ClO4 ÏàËÆ¶È:54.5% Bulletin of the Korean Chemical Society 2012 33 4150-4154 Efficient and Facile Synthesis of ¦Á-Chloroenones Bearing ¦Â-Carbonates or ¦Â-Carbamates Krishna Bahadur Somai Magar, Yong Rok Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 11 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 1977 55 2829-2834 Etude en r¨¦sonance magn¨¦tique nucl¨¦aire du 13C des param¨¨tres de substitution de la fonction azide A. Pancrazi, I. Kabor¨¦, B. Delpech, A. Astier, Q. Khuong-Huu, G. Lukacs Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 14 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 1977 55 2829-2834 Etude en r¨¦sonance magn¨¦tique nucl¨¦aire du 13C des param¨¨tres de substitution de la fonction azide A. Pancrazi, I. Kabor¨¦, B. Delpech, A. Astier, Q. Khuong-Huu, G. Lukacs Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (3S,6R)-3-isopropyl-6-(2-methyl propyl)-2,5-piperazine diketone C11H20N2O2 ÏàËÆ¶È:54.5% Chinese Traditional and Herbal Drugs 2014 45 471-475 Piperazine constituents in fruits of Physalis alkekengi var. francheti SHU Zun-peng, LI Xin-li, XU Bing-qing, WANG Qiu-hong, YANG Bing-you, KUANG Hai-xue Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Ethyl (Z)-5-(tert-butyldimethylsilyloxy)-2-pentenoate ÏàËÆ¶È:54.5% Journal of the Brazilian Chemical Society 2001 12 375-385 The Stereochemistry of the Nozaki-Hiyama-Kishi Reaction and the Construction of 10-Membered Lactones. The Enantioselective Total Synthesis of (-)-Decarestrictine D. Ronaldo A. Pilli and Mauricio M. Victor Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . »·-(ÁÁ°±Ëá-çÓ°±Ëá)-¶þëÄ ÏàËÆ¶È:54.5% Chinese Journal of Medicinal Chemistry 2012 22 38-43 Chemical constituents from the endophyte Bacillus pumilus derived from Breynia fruticosa HUO Pei-yuan; CHEN Hua-hong; JIANG Yi; HAN Li; XU Li-hua; HUANG Xue-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . »·(L-çÓ-L-ÁÁ)¶þëÄ C11H20O2N2 ÏàËÆ¶È:54.5% Chinese Journal of Marine Drugs 2013 32 31-36 ·Â´Ì²Î¹²¸½Éú·ÅÏß¾úKytococcus sp.ÖеĻ·¶þëÄ³É ¶õºã³¬, ÌÀ»ª, Áõ±¦æ, ËïÅô ÀîÁá, ÀîÖ¾ÓÂ, ÕÅÎÄ Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . compund 10b ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2002 39 1049-1054 Fused-ring nitrogen and sulfur heterocycles by a tandem SN2-michael addition reaction Richard A. Bunce, Sharadsrikar V. Kotturi, Christopher J. Peeples and Elizabeth M. Holt Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . methyl (S)-[6,7-13C2,7-siloxy-18O]-7-(tert-butyldimethylsiloxy)oct-2-enoate ÏàËÆ¶È:53.8% Tetrahedron 1998 54 15937-15958 Biosynthetic incorporation of advanced precursors into dehydrocurvularin, a polyketide phytotoxin from Alternaria cinerariae Yaoquan Liu, Zhe Li, John C. Vederas Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . ethyl (¡À)-(2E)-3-[(1R,2S)-2-(hydroxymethyl)cyclohexyl]-2-propenoate C12H20O3 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2002 39 1049-1054 Fused-ring nitrogen and sulfur heterocycles by a tandem SN2-michael addition reaction Richard A. Bunce, Sharadsrikar V. Kotturi, Christopher J. Peeples and Elizabeth M. Holt Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . ethyl (¡À)-(2E)-3-[(1R,2S)-2-(iodomethyl)cyclohexyl]-2-propenoate ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2002 39 1049-1054 Fused-ring nitrogen and sulfur heterocycles by a tandem SN2-michael addition reaction Richard A. Bunce, Sharadsrikar V. Kotturi, Christopher J. Peeples and Elizabeth M. Holt Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . (3R,5R)-(2-bromoethyl)-5-isopropenyl-2,3-dimethylcyclohexene ÏàËÆ¶È:50% Indian Journal of Chemistry Section B 2005 44B 1430-1436 Enantiospecific synthesis of B-seco-nortaxanes from two molecules of carvone Srikrishna,A; Kumar,P Praveen; Reddy,T Jagadeeswar Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . (¡À)-(1SR,3SR)-3-[3-(6-Amino-9H-9-purinyl)-propyl]-2,2-difluorocyclopropyl-methanol [= 9-[3-(3-hydroxymethyl-2,2-difluorocyclopropyl)-propyl]-adenine] C12H15ON5F2 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2004 59 77-94 Synthesis of Highly Flexible Difluorinated Cyclopropanoid Nucleoside Analogues R. Csuk and L. Eversmann Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 2-Cyano-3',4'-dimethoxy-3-(N-methylamino)cinnamic acid N-methylamide C14H17N3O3 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2009 64 662-668 Unexpected Sodium Methoxide-catalyzed Rearrangement of 6-Amino-5-aroyl-1,3-dimethyluracils to Form Novel Cinnamoamides B. Gerig, U. Girreser, C. Näther, and D. Heber Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (3S)-vinyl 6-acetyl-3-methyl-2-oxo-1,2,3,4-tetrahydrothieno[2,3-b]pyrazine-4-carboxylate C12H12N2O4S ÏàËÆ¶È:50% Heterocycles 2002 57 97-110 Preparation of Thieno[2,3-b]pyrazines as Bioisosteres for Quinoxaline Derivatives wiht Reverse Transcriptase Inhibition Thomas Erker* and Karin Trinkl Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . cyclo-(Phe-Val) C14H18O2N2 ÏàËÆ¶È:50% Natural Product Research and Development 2004 16 383-386 CYCLODIPEPTIDES FROM THE ROOTS OF PANAX NOTOGINSENG WANG Shuang-ming;TAN Ning-hua *; YANG Ya-bin; HE Min Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (R)-(E)-(+)-ethyl-5-(tert-butyldiphenylsilyloxy)-4-methyl-2-pentenoate C20H24O3Si ÏàËÆ¶È:50% Tetrahedron 2011 67 9787-9808 Studies culminating in the total synthesis and determination of the absolute configuration of (− -saudinRobert K. Boeckman Jr., Maria Rico del Rosario Ferreira, Lorna H. Mitchell, Pengcheng Shao, Michael J. Neeb, Yue Fang Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound C15H30O33Si ÏàËÆ¶È:50% The Journal of Antibiotics 2011 64 781-787 Total synthesis and absolute configuration of avenolide, extracellular factor in Streptomyces avermitilis Miho Uchida, Satoshi Takamatsu, Shiho Arima, Kiyoko T Miyamoto, Shigeru Kitani, Takuya Nihira, Haruo Ikeda and Tohru Nagamitsu Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (4R,6S)-ethyl 8-(tert-butyldimethylsilyloxy)-4-hydroxy-6-methyloct-2-enoate C17H34O4Si ÏàËÆ¶È:50% Tetrahedron 2012 68 2471-2480 Alkyl 2-(2-benzothiazolylsulfinyl)acetates as useful synthetic reagents for alkyl 4-hydroxyalk-2-enoates by sulfinyl-Knoevenagel reaction Zhenjun Du, Toshihiro Kawatani, Kazuhide Kataoka, Rikiya Omatsu, Junzo Nokami Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . (SS)-N-((R)-1-(4-(((tert-butyldimethylsilyl)oxy)methyl)thiazol-2-yl)-4-methyl-1-oxopentan-3-yl)-2-methylpropane-2-sulfinamide C20H38N2O3S2Si ÏàËÆ¶È:50% Chemistry ¨C An Asian Journal 2013 8 1213-1222 Total Synthesis of Tubulysin U and Its C-4 Epimer Xiu-dong Yang, Chang-ming Dong, Jian Chen, Ya-hui Ding, Qi Liu, Xiao-yan Ma, Dr. Quan Zhang and Prof. Yue Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . ethyl (R,Z)-5-(tert-butyldimethylsilyloxy)hex-2-enoate C14H28O3Si ÏàËÆ¶È:50% Tetrahedron 2014 70 1199-1206 Synthesis of highly substituted pyranonaphthalene spiroketals related to the griseusins using a Hauser¨CKraus annulation strategy Briar J. Naysmith, Daniel Furkert, Margaret A. Brimble Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . pestalotiopamide B ÏàËÆ¶È:50% Journal of Asian Natural Products Research 2011 13 373-376 Pestalotiopamide E, a new amide from the endophytic fungus Pestalotiopsis sp. Jing Xu; Qiang Lin; Bin Wang; Victor Wray; Wen-Han Lin; Peter Proksch Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . compound 11 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 1996 34 660-666 13C NMR and 1H NMR Study of Substituted Tricyclic [2+2] Photoadducts Gordon L. Lange and Christine Gottardo Structure 13C NMR ̼Æ×Ä£Äâͼ Copyright © 2009-2011 ÉϺ£Î¢Æ×ÐÅÏ¢¼¼ÊõÓÐÏÞ¹«Ë¾ Shanghai Micronmr Infor Technology Co., Ltd., All Rights Reserved µØÖ·£ºÉϺ£ÊÐÑîÆÖÇøºªµ¦Â·100ºÅ61¶°131ÊÒ(¸´µ©¿Æ¼¼Ô°), Óʱà:200437 E-mail: micronmr@126.com ×Éѯµç»°:086-021-61736083 »¦ICP±¸10026489ºÅ |
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-Dendroprimine and Isomers
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