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µÚÒ»¸ö: 13.3, 18.5, 22.6, 24.0, 26.3, 28.8, 29.0, 35.6, 41.5, 44.2, 46.6, 50.9, 52.1, 57.6, 71.3, 79.1, 79.4, 81.5, 168.8, 208.6, 213.9 µÚ¶þ¸ö: 10.4, 13.0, 18.6, 21.9, 26.6, 28.3, 29.0, 35.2, 39.8, 42.6, 44.2, 46.6, 48.3, 50.4, 57.6, 74.5, 79.3, 81.8, 168.8, 209.0, 213.0 |
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²éѯ½á¹û£º¹²²éµ½300¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (3R,4R,5S)-ethyl 4-acetamido-5-[(tert-butoxycarbonyl)amino]-3-(pentan-3-yloxy)-2-[2-(triethoxysilyl)ethyl]cyclohex-1-enecarboxylate C29H54N2O9Si ÏàËÆ¶È:66.6% Heterocycles 2012 86 1565-1574 SYNTHESIS OF A NEW OSELTAMIVIR DERIVATIVE THROUGH LATE-STAGE CATALYTIC C¨CH FUNCTIONALIZATION Kenta Saito and Motomu Kanai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . gymnandine C22H33NO ÏàËÆ¶È:63.6% Acta Pharmaceutica Sinica 1993 28 188-191 DITERPENOID ALKALOIDS FROM ACONITUM GYMNANDRUM LS Ding; FE Wu and YZ Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 7¦Â,8¦Â-dihydroxystemodin C20H34O4 ÏàËÆ¶È:61.9% Journal of Natural Products 1991 Vol 54 1543 Preparation, Characterization, and Antiviral Activity of Microbial Metabolites of Stemodin Charles D. Hufford, Farid A. Badria, Mohamed Abou-Karam, W. Thomas Shier, Robin D. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . eriocalyxin C C22H28O7 ÏàËÆ¶È:59.0% Journal of Natural Products 1999 62 782-784 Diterpenoids from Isodon eriocalyx Shao-Nong Chen, Jian-Min Yue, Shao-Yuan Chen, Zhong-Wen Lin, Guo-Wei Qin, Han-Dong Sun, and Yao-Zu Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . eriocalyxin C C22H28O7 ÏàËÆ¶È:59.0% Chinese Chemical Letters 1998 9 1025-1028 Three New Diterpenoids from Isodon Eriocalyx shao Nong CHEN,Shao Yuan CHEN,Jian Min YUE,Zhong Wen LIN,Guo Wei QIN,Han Dong SUN,and Yao Zu CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 9-deoxyforskolin ÏàËÆ¶È:59.0% Phytochemistry 1989 28 859-862 Minor diterpenoids of Coleus forskohlii Bruno Gabetta,Gianfranco Zini,Bruno Danieli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . aconicarmine C22H35NO5 ÏàËÆ¶È:59.0% Molecules 2012 17 9939-9946 Alkaloids Isolated from the Lateral Root of Aconitum carmichaelii Liang Xiong, Cheng Peng, Xiao-Fang Xie, Li Guo, Cheng-Jun He, Zhao Geng, Feng Wan, Ou Dai and Qin-Mei Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 19b C24H36O9 ÏàËÆ¶È:58.3% 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 -------------------------------------------------------------------------------- 9 . compound 19b C24H36O9 ÏàËÆ¶È:58.3% 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 -------------------------------------------------------------------------------- 10 . shinjuglycoside D ÏàËÆ¶È:57.6% Chemical & Pharmaceutical Bulletin 1987 35 4302-4306 Bitter Principles of Ailanthus altissima SWINGLE. Structure Determination of Shinjuglycosides E and F YOSHIO NIIMI,TAKAHIKO TSUYUKI,TAKEYOSHI TAKAHASHI and KAZUHIRO MATSUSHITA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . shinjuglycoside D C20H28O6 ÏàËÆ¶È:57.6% Bulletin of the Chemical Society of Japan 1984 57 2496-2501 Constituents of Seeds of Ailanthus altissima SWINGLE. Isolation and Structures of Shinjuglycosides A, B, C, and D Shin Yoshimura, Masami Ishibashi, Takahiko Tsuyuki, Takeyoshi Takahashi, Kazuhiro Matsushita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 7¦Â,13-dihydroxystemodan-2-one ÏàËÆ¶È:57.1% Phytochemistry 2005 66 1898-1902 Stemodane and stemarane diterpenoid hydroxylation by Mucor plumbeus and Whetzelinia sclerotiorum Avril R.M. Chen, Peter L.D. Ruddock, Andrew S. Lamm,William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . diacarperoxide B C20H34O6 ÏàËÆ¶È:57.1% Journal of Natural Products 2008 71(8) 1358-1364 Diacarperoxides, Norterpene Cyclic Peroxides from the Sponge Diacarnus megaspinorhabdosa Sabrin R. M. Ibrahim, Rainer Ebel, Victor Wray, Werner E. G. M¨¹ller, RuAngelie Edrada-Ebel, and Peter Proksch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . scabrolide C C20H26O6 ÏàËÆ¶È:57.1% Journal of Natural Products 2002 65 1904-1908 Scabrolides A-D, Four New Norditerpenoids Isolated from the Soft Coral Sinularia scabra Jyh-Horng Sheu,Atallah F. Ahmed, Ru-Ting Shiue, Chang-Feng Dai, and Yao-Haur Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . aikupikoxide C C20H34O6 ÏàËÆ¶È:57.1% Journal of Natural Products 2001 64 1332-1335 Cytotoxic Cyclic Norterpene Peroxides from a Red Sea Sponge Diacarnus erythraenus Diaa T. A. Youssef,Wesley Y. Yoshida, Michelle Kelly, and Paul J. Scheuer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . compound 1 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1980 28 365-371 Carbon-13 Nuclear Magnetic Resonance Spectral Assignments of Grayanotoxin-I NAOHIRO SHIRAI,HISAO NAKATA,TOYO KAIYA and JINSAKU SAKAKIBARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . De-A,B-24-oxo-23,25-(isopropylidenedioxy)-cholestan-8-ol C20H33O4 ÏàËÆ¶È:57.1% Steroids 2000 65 252-265 Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3 Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . De-A,B-24-oxo-23,25-(isopropylidenedioxy)-cholestan-8-one C21H35O4 ÏàËÆ¶È:57.1% Steroids 2000 65 252-265 Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3 Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (13S,14S)-14-Hydroxy-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstan-17-one 17-oxime ÏàËÆ¶È:57.1% Steroids 2004 69 511-514 Reaction of (13S)-13-iodo-6¦Â-methoxy-3¦Á,5-cyclo-13,14-seco-5¦Á-androstane-14,17-dione with hydroxylamine and its application to the synthesis of new 13,14-seco steroids Vladimir A. Khripach, Vladimir N. Zhabinskii, Anna I. Kuchto, Galina P. Fando, Yuliya Y. Zhiburtovich, Alexander S. Lyakhov, Alla A. Govorova, Marinus B. Groen, Jaap van der Louw, Aede de Groot Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . ring B-homo derivative ÏàËÆ¶È:57.1% Natural Product Research 1993 1 257-262 Rearrangements of Derivatives of Methyl 9,11-Dihydroxy-(-)-Kauran-19-Oate to New Skeletal Diterpenes Tatsuhiko Nakano; Maria Aracelis Maillo; Alfredo Usubillaga; Andrew T. McPhail; Donald R. McPhail Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . torilolone 11-O-¦Â-D-glucopyranoside C21H34O8 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1998 46 1743-1747 New Guaiane-Type Sesquiterpenoid Glycosides from Torillis japonica Fruit Junichi KITAJIMA,Nobuyuki SUZUKI and Yasuko TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-12 09:46:07
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
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chenjjun1982: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-12 10:22:49
chenjjun1982: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-12-12 10:22:49
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²éѯ½á¹û£º¹²²éµ½553¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . amarolide 11-acetate ÏàËÆ¶È:72.7% Bulletin of the Chemical Society of Japan 1984 57 2496-2501 Constituents of Seeds of Ailanthus altissima SWINGLE. Isolation and Structures of Shinjuglycosides A, B, C, and D Shin Yoshimura, Masami Ishibashi, Takahiko Tsuyuki, Takeyoshi Takahashi, Kazuhiro Matsushita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . amarolide C20H2706 ÏàËÆ¶È:71.4% Journal of Natural Products 1996 59 73-76 A New Quassinoid from Castela texana Jinhui Dou, James D. McChesney, Robert D. Sindelar, D. Keith Goins, and Larry A. Walker Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . chaparramarin C20H28O6 ÏàËÆ¶È:71.4% Phytochemistry 1992 31 3262-3264 Structure of chaparramarin, a quassinoid from Castela tortuosa Isao Kubo, Yoshihiro Murai, Swapan K. Chaudhuri Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . shinjuglycoside D ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 1987 35 4302-4306 Bitter Principles of Ailanthus altissima SWINGLE. Structure Determination of Shinjuglycosides E and F YOSHIO NIIMI,TAKAHIKO TSUYUKI,TAKEYOSHI TAKAHASHI and KAZUHIRO MATSUSHITA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . shinjuglycoside D C20H28O6 ÏàËÆ¶È:69.2% Bulletin of the Chemical Society of Japan 1984 57 2496-2501 Constituents of Seeds of Ailanthus altissima SWINGLE. Isolation and Structures of Shinjuglycosides A, B, C, and D Shin Yoshimura, Masami Ishibashi, Takahiko Tsuyuki, Takeyoshi Takahashi, Kazuhiro Matsushita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . amarolide ÏàËÆ¶È:66.6% Bulletin of the Chemical Society of Japan 1984 57 2496-2501 Constituents of Seeds of Ailanthus altissima SWINGLE. Isolation and Structures of Shinjuglycosides A, B, C, and D Shin Yoshimura, Masami Ishibashi, Takahiko Tsuyuki, Takeyoshi Takahashi, Kazuhiro Matsushita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . paraine C21H28O6 ÏàËÆ¶È:66.6% Pharmaceutical Biology 1996 34 349-354 A New Quassinoid from Crude Quassin-extract of Quassia amara Dou J., McChesney J.D., Sindelar R.D., Goins D.K., Khan I.A., Walker L.A. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . methyl 7¦Á-tert-butyldimethylsilyloxy-8,13-dioxo-14,15,17-trinorlabdan-19-oate C24H42O5Si ÏàËÆ¶È:63.6% Journal of Natural Products 2006 69(4) 563-566 A New Route toward 7-Oxo-13-hydroxy-8,11,13-podocarpatrienes from Labdane Diterpenes Enrique Alvarez-Manzaneda Roldn, Juan Luis Romera Santiago, and Rachid Chahboun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . virescenine ÏàËÆ¶È:61.9% Chemistry of Natural Compounds 1981 17 345-348 STRUCTURES OF MONTIGAMINE AND MONTICOLINE E. F. Ametova, M. S. Yunusov, V. E. Bannikova, N. D. Abdullaev, and V. A. Tel'nov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . Cinncassiol D4 2-0-monoacetate C22H34O6 ÏàËÆ¶È:61.9% Phytochemistry 1982 21 2130-2132 Two novel diterpenes from bark of Cinnamomum cassia Toshihiro Nohara, Yoshiki Kashiwada, Toshiaki Tomimatsu, Itsuo Nishioka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 4 ÏàËÆ¶È:61.9% Tetrahedron 1996 52 13981-13990 Bioconversion of 17¦Â-hydroxy-17¦Á-methyl-androsta-1,4-dien-3-one and androsta-1,4-diene-3,17-dione in cultures of the green alga T76 Scenedesmus quadricauda Marina DellaGreca, Lucio Previtera, Antonio Fiorentino, Gabriele Pinto, Antonino Pollio Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . virescenine ÏàËÆ¶È:60.8% Helvetica Chimica Acta 2009 92 629-637 Diterpenoid and Norditerpenoid Alkaloids from the Roots of Aconitum yesoense var. macroyesoense Koji Wada, Norio Kawahara Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 15¦Á-hydroxy-cardenolide ÏàËÆ¶È:60.8% Phytochemistry 1998 49 273-275 A cardenolide glycoside from gomphocarpus sinaicus Nahla S. Abdel-Azim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . gymnandine C22H33NO ÏàËÆ¶È:59.0% Acta Pharmaceutica Sinica 1993 28 188-191 DITERPENOID ALKALOIDS FROM ACONITUM GYMNANDRUM LS Ding; FE Wu and YZ Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . delavaconine ÏàËÆ¶È:59.0% Heterocycles 1990 31 1517-1524 Studies on the Alkaloids from Aconitum contortum (I) Kazuaki Niitsu, Yukinobu Ikeya, Hiroshi Mitsuhashi, Chen Siying, and Liang Huiling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . delavaconine C22H35NO5 ÏàËÆ¶È:59.0% Acta Chimica Sinica 1987 45 1101-1106 Studies on the Chinese Drug, Aconitum Spp.XIV. Studies on the Chemical Structure of Delavaconitine Jing Shan-Hao Hong Shah-Hai Zhou Bing-Nan Zhu Yuan-Long Zhu Ren-Hong Zheng Pei-Ju Wang Ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 10 C26H44NO7S ÏàËÆ¶È:57.6% Journal of Asian Natural Products Research 2008 10 1063-1067 An effective O-demethylation of some C19-diterpenoid alkaloids with HBr-glacial acetic acid Chun-Lan Zou, Hong Ji, Guang-Bo Xie, Dong-Lin Chen and Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . diacarperoxide B C20H34O6 ÏàËÆ¶È:57.1% Journal of Natural Products 2008 71(8) 1358-1364 Diacarperoxides, Norterpene Cyclic Peroxides from the Sponge Diacarnus megaspinorhabdosa Sabrin R. M. Ibrahim, Rainer Ebel, Victor Wray, Werner E. G. M¨¹ller, RuAngelie Edrada-Ebel, and Peter Proksch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 9¦Â-hydroxy-2¦Â-methoxyclovan-10-one C16H26O3 ÏàËÆ¶È:57.1% Journal of Natural Products 2004 67 793-798 Structure−Activity Relationships in the Fungistatic Activity against Botrytis cinerea of Clovanes Modified on Ring C Athina Deligeorgopoulou, Antonio J. Macas-Snchez, Daniel J.Mobbs, Peter B. Hitchcock, James R. Hanson, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . aikupikoxide C C20H34O6 ÏàËÆ¶È:57.1% Journal of Natural Products 2001 64 1332-1335 Cytotoxic Cyclic Norterpene Peroxides from a Red Sea Sponge Diacarnus erythraenus Diaa T. A. Youssef,Wesley Y. Yoshida, Michelle Kelly, and Paul J. Scheuer Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-12-12 09:46:20














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