| ²é¿´: 391 | »Ø¸´: 1 | |||
°²°²anan_tbгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
ÇóÖú΢Æ×½âÎö»¯ºÏÎлл ÒÑÓÐ1È˲ÎÓë
|
|
Ãû³Æ£ºBMQ2 ÈܼÁ£ºÂÈ·Â 13C-NMRÊý¾Ý£º8.48,19.91,22.90,35.84,47.22,72.27,78.20,120.17,163.08,175.19 °ÝÍи÷λ°ï棬лл |
» ²ÂÄãϲ»¶
ÉúÎïѧ303Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÖÐũ΢ÉúÎÁù¼¶Òѹý£¬ÓпÆÑÐÓÐÎÄÕ£¬µ³Ô±
ÒѾÓÐ4È˻ظ´
318Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
0703µ÷¼Á
ÒѾÓÐ11È˻ظ´
»¯Ñ§357·Ö£¬¿¼Ñе÷¼Á
ÒѾÓÐ10È˻ظ´
0854Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
272Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
µ÷¼ÁÇóÖú
ÒѾÓÐ13È˻ظ´
332Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
341Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸µç×ӿƼ¼´óѧ085600²ÄÁÏÓ뻯¹¤ 329·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú1¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
ÇóÖú3¸ö΢ÆÕÊý¾Ý
ÒѾÓÐ5È˻ظ´
ÇóÖúάÆ×Êý¾Ý¿â
ÒѾÓÐ5È˻ظ´
΢Æ×Êý¾Ý¡£Ç󻯺ÏÎï½âÎö
ÒѾÓÐ3È˻ظ´
ÇóÍÆ¼ö¹ØÓÚ»¯ºÏÎï½á¹¹Óë»îÐÔ¹ØÏµµÄÆÚ¿¯
ÒѾÓÐ4È˻ظ´
ÇóÖúÓÃCDÆ×½âÎöÒ»¸öÄ¾Ö¬ËØÀ໯ºÏÎïµÄ¾ø¶Ô¹¹ÐÍ
ÒѾÓÐ7È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
ÇëÎÊÓÐûÓÐÒ»¸ö»¯ºÏÎï±ê×¼Æ×ͼ½âÎöÊý¾Ý¿â£¿
ÒѾÓÐ5È˻ظ´
¡¾·ÖÏí¡¿Ãâ·ÑµÄ20¸öÆ×ͼÊý¾Ý¿â
ÒѾÓÐ13È˻ظ´
׿Խ_ÏÈ·æ
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
ºýÍ¿³æ
- Ó¦Öú: 990 (²©ºó)
- ¹ó±ö: 2.955
- ½ð±Ò: 6796.4
- É¢½ð: 12161
- ºì»¨: 82
- ɳ·¢: 17
- Ìû×Ó: 3017
- ÔÚÏß: 2457Сʱ
- ³æºÅ: 1713223
- ×¢²á: 2012-03-24
- ÐÔ±ð: GG
- רҵ: ÁÙ´²Ò©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
°²°²anan_tb: ½ð±Ò+8, ¡ïÓаïÖú 2015-05-11 21:43:35
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
°²°²anan_tb: ½ð±Ò+8, ¡ïÓаïÖú 2015-05-11 21:43:35
|
²éѯ½á¹û£º¹²²éµ½40¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3-hydroxy-4(8)-ene-p-menthane-3(9)-lactone ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2002 33 8-11 Monoterpenoids from Schizonepeta tenuifolia YANG Fan; ZHANG Ren-yan; CHEN Jiang-tao; YANG Chong-ren Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ent-8,8a-dihydro-ramulosin C10H16O3 ÏàËÆ¶È:70% The Journal of Antibiotics 1999 52 1124-1134 Biomolecular-chemical Screening: A Novel Screening Approach for the Discovery of Biologically Active Secondary Metabolites III. New DNA-binding Metabolites CORINNA MAUL, ISABEL SATTLER, MARION ZERLIN, CLAUDIA HINZE, CORINNA KOCH, ARMIN MAIER, SUSANNE GRABLEY, RALF THIERICKE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 1,2-dihydroxymintlactone ÏàËÆ¶È:70% Chinese Journal of Natural Medicines 2013 11 71-73 A new menthane-type monoterpene from Pleurotus eryngii LIU Liang-Yan, LI Zheng-Hui, LIU Ji-Kai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (+)-3-hydroxymintlatone ÏàËÆ¶È:70% Journal of Oleo Science 2003 52 483-489 Terpenoids in Volatile Oil from Bursera graveolens Chiyoki YUKAWA, Hisakatsu IWABUCHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (+)-mintlactone ÏàËÆ¶È:70% Journal of Oleo Science 2003 52 483-489 Terpenoids in Volatile Oil from Bursera graveolens Chiyoki YUKAWA, Hisakatsu IWABUCHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-mintlactone C10H14O2 ÏàËÆ¶È:70% Chromatographia 2013 76 491-498 Qualitative and Quantitative Studies on Impurities in Schizonepetin, a Novel Antiviral Agent, Using HPLC, NMR and MS Dongliang Liu, Mingqiu Shan, Peidong Chen, Li Zhang, Anwei Ding Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,2-Dihydroxymintlactone C10H14O4 ÏàËÆ¶È:70% Zeitschrift f¨¹r Naturforschung C 1995 50 473-475 1,2-Dihydroxymintlactone, a New Nematicidal Monoterpene Isolated from the Basidiomycete Cheimonophyllum candidissimum (Berk & Curt.) Sing. Marc Stadler, Jean-Yves Fouron, Olov Sterner and Heidrun Anke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 4¦Á-Hydroxy-5¦Á,8¦Á(H)-eudesm-7(11)-en-8,12-olide C15H22O3 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2010 93 803-810 Terpenoids from Roots of Chloranthus spicatus Zhi-Yong Xiao, Xia-Chang Wang, Gui-Ping Zhang, Zhong-Liang Huang and Li-Hong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . isopropyl 2-hydroxy-2-(4-fluorophenyl)butanoate C13H17O3F ÏàËÆ¶È:63.6% molecules 2011 16 5020-5034 Ru/Me-BIPAM-Catalyzed Asymmetric Addition of Arylboronic Acids to Aliphatic Aldehydes and ¦Á-Ketoesters Yasunori Yamamoto, Tomohiko Shirai, Momoko Watanabe, Kazunori Kurihara and Norio Miyaura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound IV-Cl ÏàËÆ¶È:63.6% Tetrahedron 2013 69 4883-4889 Unusual rearrangement and dearomatization reactions in Cu(I)-catalyzed atom transfer radical cyclizations from N-(1-phenylethyl)trichloroacetamides Faïza Diaba, Juan A. Montiel, Josep Bonjoch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 2¦Â-hydroxycamphor ÏàËÆ¶È:60% Phytochemistry 2001 57 669-673 Biotransformation of (+)- and (-)-camphorquinones by plant cultured cells Wen Chai, Hiroki Hamada, Jumpei Suhara, C.Akira Horiuchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . MKN-004B C10H18O3 ÏàËÆ¶È:60% Journal of Natural Products 2001 64 664-667 New Lactone-Containing Metabolites from a Marine-Derived Bacterium of the Genus Streptomyces Ki Woong Cho, Hyi-Seung Lee, Jung-Rae Rho, Tae Sik Kim, Sang Jun Mo, and Jongheon Shin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 6-Desoxy-6-brom-L-ascorbinsaure C6H7BrO5 ÏàËÆ¶È:60% Helvetica Chimica Acta 1980 63 1728-1739 Synthese und Eigenschaften von 6-Desoxy-6-halogen-Derivaten der L-Ascorbinsäure Joseph Kiss, Klaus Peter Berg, Adolf Dirscherl, Willi E. Oberhänsli, Wolf Arnold Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . gentiolactone ÏàËÆ¶È:60% Phytochemistry 1997 46 1035-1038 Secoiridoids from Gentiana siphonantha Ren Xiang Tan, Ling Dong Kong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 13-nor-8(11)-dihydropilocarpine ÏàËÆ¶È:60% Phytochemistry 1996 42 885-887 An imidazole alkaloid and other constituents from Pilocarpus trachyllophus Manoel Andrade-Neto, Paulo Henriques Mendes, Edilberto Rocha Silveira Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (E)-3-(amino(morpholino)methylene)-1-cyclpropancarbonyl-2-pyrrolidinone C13H19N3O3 ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2007 44 227-230 Synthesis of ¦Á-diaminomethylenebutyrolactams by the reaction of-cyanobutyrolactams with n-trimethylsilylamines Fumi Okabe,Syouhei Nakamura and Kenji Yamagata Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 4¦Á-Hydroxy-5¦Á,8¦Â(H)-eudesm-7(11)-en-8,12-olide C15H22O3 ÏàËÆ¶È:60% Helvetica Chimica Acta 2010 93 803-810 Terpenoids from Roots of Chloranthus spicatus Zhi-Yong Xiao, Xia-Chang Wang, Gui-Ping Zhang, Zhong-Liang Huang and Li-Hong Hu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 1¦Â,4¦Á-dihydroxy-5¦Á,8¦Â(H)-eudesm-7 C15H22O4 ÏàËÆ¶È:60% Acta Botanica Yunnanica 2010 32 83-86 A New Phenolic Glycoside from Chloranthusmul tistachys (Chloranthaceae) RAN Xin-Hui, N I Wei, WEI Gang, CHEN Chang-Xiang, LIU Hai-Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 14c C9H12O2 ÏàËÆ¶È:60% Tetrahedron Letters 2003 44 5727-5730 Synthesis of alkylated iridolactone analogs Zineb Guerrab, Boujemaa Daou, Souad Fkih-Tetouani, Mohammed Ahmar, Bernard Cazes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . zedoalactone C ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2008 25 188-190 Guaiane sesquiterpenes of Curcuma wenyujin HU Dan, MA Ning, LOU Yan, QU Ge-xia, QIU Feng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . (1R,2R,6S)-6-[(1S)-2-chloro-1-hydroxyethyl]-2-methylcyclohex-3-ene-1-carbonitrile C10H14ClNO ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2010 46 1151-1156 Eleuthesides and their analogs: I. Synthesis of the base compound from levoglucosenone adduct with piperylene Yu. A. Kondrova, O. Yu. Krasnoslobodtseva, L. V. Spirikhin and F. A. Valeev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . 6,6'-(1,4-dihydroxybutan-1,4-diyl)bis-[(1R,2R,6S)-2-methylcyclohex-3-ene-1-carbonitrile] C20H28N2O2 ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2010 46 1151-1156 Eleuthesides and their analogs: I. Synthesis of the base compound from levoglucosenone adduct with piperylene Yu. A. Kondrova, O. Yu. Krasnoslobodtseva, L. V. Spirikhin and F. A. Valeev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . 6-(1'-hydroxypropyl)-8-methylisoxanthopterin C10H13N5O3 ÏàËÆ¶È:60% Experientia 1981 37 679-680 Lucibufagins, IV. New defensive steroids and a pterin from the firefly,Photinus pyralis (coleoptera: Lampyridae) M. A. Goetz, J. Meinwald and T. Eisner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . schizonepetin ÏàËÆ¶È:60% Chromatographia 2013 76 491-498 Qualitative and Quantitative Studies on Impurities in Schizonepetin, a Novel Antiviral Agent, Using HPLC, NMR and MS Dongliang Liu, Mingqiu Shan, Peidong Chen, Li Zhang, Anwei Ding Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . vibralactone H C10H16O4 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2012 14 115-120 Vibralactones G¨CJ from cultures of the basidiomycete Boreostereum vibrans Gang-Qiang Wang, Kun Wei, Tao Feng, Zheng-Hui Li, Lin Zhang, Qiu-An Wang & Ji-Kai Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . (2S,4R,6R)-6-(Cyanomethyl)-4-hydroxy-5,5-dimethyltetrahydro-2H-pyran-2-carboxamide C10H16N2O3 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2012 1217-1222 An Ammonia-Triggered Stereocontrolled Conversion of a -Lactone to the Central Tetrahydropyran of Pederin, Psymberin, and Onnamides D¨CF William J. Buffham, Nigel A. Swain, Sarah L. Kostiuk, Th¨¦o P. Gonçalves and David C. Harrowven Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . (2S,4R,6S)-6-(Cyanomethyl)-4-hydroxy-5,5-dimethyltetrahydro-2H-pyran-2-carboxamide C10H16N2O3 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2012 1217-1222 An Ammonia-Triggered Stereocontrolled Conversion of a -Lactone to the Central Tetrahydropyran of Pederin, Psymberin, and Onnamides D¨CF William J. Buffham, Nigel A. Swain, Sarah L. Kostiuk, Th¨¦o P. Gonçalves and David C. Harrowven Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . (2S,4R)-7-Cyano-2,4-dihydroxy-5,5-dimethylhept-6-enamide C10H16N2O3 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2012 1217-1222 An Ammonia-Triggered Stereocontrolled Conversion of a -Lactone to the Central Tetrahydropyran of Pederin, Psymberin, and Onnamides D¨CF William J. Buffham, Nigel A. Swain, Sarah L. Kostiuk, Th¨¦o P. Gonçalves and David C. Harrowven Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . (3-Methyloxetan-3-yl)methyl 6-iodohexanoate ÏàËÆ¶È:60% Steroids 2012 77 1113-1122 Design, synthesis, cytocidal activity and estrogen receptor ¦Á affinity of doxorubicin conjugates at 16¦Á-position of estrogen for site-specific treatment of estrogen receptor positive breast cancer Pijus Saha, S¨¦bastien Fortin, Val¨¦rie Leblanc, Sophie Parent, ¨¦ric Asselin, Gervais B¨¦rub¨¦ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 30 . Methyl (2S,3S)-3-Hydroxy-2-methyl-7-octynoate C10H16O3 ÏàËÆ¶È:60% Journal of the American Chemical Society 1996 118 11635-11643 Onchidin B: A New Cyclodepsipeptide from the Mollusc Onchidium sp. Rogelio Fern¨¢ndez, Jaime Rodr¨ªguez, Emilio Quiño¨¢, Ricardo Riguera, Luis Muñoz, Miryam Fern¨¢ndez-Su¨¢rez, and C¨¦cile Debitus Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 31 . Methyl (2R,3R)-3-Hydroxy-2-methyl-7-octynoate C10H16O3 ÏàËÆ¶È:60% Journal of the American Chemical Society 1996 118 11635-11643 Onchidin B: A New Cyclodepsipeptide from the Mollusc Onchidium sp. Rogelio Fern¨¢ndez, Jaime Rodr¨ªguez, Emilio Quiño¨¢, Ricardo Riguera, Luis Muñoz, Miryam Fern¨¢ndez-Su¨¢rez, and C¨¦cile Debitus Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 32 . Multistalactone B C15H20O4 ÏàËÆ¶È:60% Phytochemistry 2013 88 112-118 Sesquiterpenoids from Chloranthus multistachys Hai-Yang Liu, Xin-Hui Ran, Ning-Bo Gong, Wei Ni, Xu-Jie Qin, Yan-Yan Hou, Yang L¨¹, Chang-Xiang Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 33 . Multistalactone C C15H20O4 ÏàËÆ¶È:60% Phytochemistry 2013 88 112-118 Sesquiterpenoids from Chloranthus multistachys Hai-Yang Liu, Xin-Hui Ran, Ning-Bo Gong, Wei Ni, Xu-Jie Qin, Yan-Yan Hou, Yang L¨¹, Chang-Xiang Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 34 . (6R,7R) and (6R,7S)-5,6,7,7a-tetrahydro-7a-hydroxy-3,6-dimethyl-4h-benzofuran-2-one ÏàËÆ¶È:60% Flavour and Fragrance Journal 2002 17 218-226 Menthofurolactone: a new p-menthane lactone in Mentha piperita L.: analysis, synthesis and olfactory properties Eric Fr¨¦rot, Alain Bagnoud and Christine Vuilleumier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 35 . 4(R),15-epoxy-atractylenolide II [4(R),15-epoxy-eudesma-7(11)-en-8¦Á,12-olide] C15H20O3 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2013 15 344-356 Four new eudesmane-type sesquiterpenoid lactones from atractylenolide II by biotransformation of rat hepatic microsomes Ying Li, Jing Liu & Xiu-Wei Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 36 . zedoalactone C ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2011 42 1079-1082 Chemical constituents from Paraixeris serotina XU, Guo-xi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 37 . gentiolactone ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2011 36 2215-2218 Chemical constituents of Swertia hispidicalyx JIANG, Fuqiang, ZHANG, Xuemei, MA, Yunbao, GENG, Chang'an, JIANG, Zhiyong, CHEN, Jijun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 38 . (4R,7R)-8-Carboxy-7,9-dihydroxy-trans-menthane C10H18O4 ÏàËÆ¶È:60% Natural Product Research 2013 27 1994-1998 Zantholic acid, a new monoterpenoid from Zanthoxylum zanthoxyloides N.A. Vyry Wouatsa, L.N. Misra, R. Venkatesh Kumar, Mahendra P. Darokar & Francois Tchoumbougnang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 39 . methyl 3-cyclohexyl-3-hydroxy-2-methylpropanoate C10H18O3 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2014 62 956-961 Asymmetric Reductive Aldol-Type Reaction with Carbonyl Compounds Using Dialkyl Tartrate as a Chiral Ligand Motoyuki Isoda, Kazuyuki Sato, Yoriko Tokura, Atsushi Tarui, Masaaki Omote, Akira Ando Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-04-01 14:53:07














»Ø¸´´ËÂ¥
5