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chenjjun1982

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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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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-12-12 09:46:07
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
3Â¥2013-12-12 09:46:20
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