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361810541

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13C NMR (101 MHz, CDCl3) ¦Ä16.08, 19.23,21.19, 26.17, 27.54, 29.06, 30.26, 34.89, 35.75, 38.51, 43.43, 52.25, 53.33, 56.66, 62.80, 75.97, 77.23, 82.98, 99.42, 127.27, 129.02, 135.57, 136.41 ,170.61,175.78,204.29
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1 .     berkeleyacetal A
C26H32O8     ÏàËÆ¶È:80.7%
Journal of Natural Products          2007          70          1820-1823
The Berkeleyacetals, Three Meroterpenes from a Deep Water Acid Mine Waste Penicillium
Donald B. Stierle,Andrea A. Stierle, and Brianna Patacini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     epoxycytochalasin H
    ÏàËÆ¶È:60.7%
Journal of Agricultural and Food Chemistry          1982          30          301-304
Isolation and identification of two new [11]cytochalasins from Phomopsis sojae
Richard J. Cole, David M. Wilson, James L. Harper, Richard H. Cox, Teena W. Cochran, Horace G. Cutler, Durham K. Bell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (2S,4aR,6aR,7R,9S,10aS,10bR)-Methyl 9-acetoxy-6a,10bdimethyl-4,10-dioxo-2-((S)-1-((R)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoyloxy)but-3-enyl)dodecahydro-1Hbenzo[f]isochromene-7-carboxylate
    ÏàËÆ¶È:58.0%
Organic & Biomolecular Chemistry          2009          7          3748-3756
Synthetic studies of neoclerodane diterpenes from Salvia divinorum: role of the furan in affinity for opioid receptors
Denise S. Simpson, Kimberly M. Lovell, Anthony Lozama, Nina Han, Victor W. Day, Christina M. Dersch, Richard B. Rothman and Thomas E. Prisinzano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     methyl 6¦Â,15-diacetoxy-7-labden-17-oate
    ÏàËÆ¶È:57.6%
Phytochemistry          1989          28          557-560
Minor labdane diterpenoids from Halimium verticillatum
Julio G. Urones,Isidro S. Marcos,David D. Martin,Maria C. Alonso Alonso,Fernando M.S. Brito Palma,Jesus M.L. Rodilla
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Emeriphenolicin B
C24H34NO5Cl     ÏàËÆ¶È:57.6%
Phytochemistry          2011          72          1436-1442
Antiviral isoindolone derivatives from an endophytic fungus Emericella sp. associated with Aegiceras corniculatum
Guojian Zhang, Shiwei Sun, Tianjiao Zhu, Zhenjian Lin, Jingyan Gu, Dehai Li ⇑, Qianqun Gu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     deacetylepoxycytochalasin H
    ÏàËÆ¶È:57.6%
Journal of Agricultural and Food Chemistry          1982          30          301-304
Isolation and identification of two new [11]cytochalasins from Phomopsis sojae
Richard J. Cole, David M. Wilson, James L. Harper, Richard H. Cox, Teena W. Cochran, Horace G. Cutler, Durham K. Bell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 1a
C24H36O6     ÏàËÆ¶È:57.6%
Magnetic Resonance in Chemistry          2012          50          709-712
Structure elucidation and NMR assignments of an unusual aromatic monacolin analog from Monascus purpureus-fermented rice
Ming-Tao Liu, Na Luan, Jin-Jie Li, Xiao Huang, Ye-Feng Wang, A-Li Wang and Xiao-Ya Shang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Methyl (E)-9-[(1S,2R,3R,5S)-2-(2-Acetoxyethyl)-3,5-bis(tert-butyldimethylsilyloxy)cyclopentyl]-7-(tert-butyldimethylsilyloxy)non-8-enoate
C37H74O7Si3     ÏàËÆ¶È:57.1%
European Journal of Organic Chemistry          2012                   2621-2634
Total Synthesis of Isoprostanes Derived from Adrenic Acid and EPA
Camille Oger, Val¨¦rie Bultel-Ponc¨¦, Alexandre Guy, Thierry Durand and Jean-Marie Galano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 26b
C26H37NO6     ÏàËÆ¶È:57.1%
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   Ì¼Æ×Ä£Äâͼ
10 .     6,12,13,14-Diepoxycytochalasin B
C29H37NO7     ÏàËÆ¶È:55.5%
Magnetic Resonance in Chemistry          2008          46          650-659
Synthesis, complete 1H and 13C NMR assignment and crystal structure of novel epoxide derivatives of cytochalasin B (pages 650¨C659)
Pieter S. Steyn, Jaco C. Breytenbach, Jeanne H. Botha, Manuel A. Fernandes and Philippus L. Wessels
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 1
C56H80N2O14S4     ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2009          17          7435-7440
Synthesis and biological evaluation of epothilone A dimeric compounds
Daniele Passarella, Daniela Comi, Graziella Cappelletti, Daniele Cartelli, Juerg Gertsch, Ana R. Quesada, Jurgen Borlak, Karl-Heinz Altmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     13-acetoxy-20-O-angelylingenol
C27H36O8     ÏàËÆ¶È:55.5%
Chinese Chemical Letters          2011          22          451-454
Isolation and characterization of ingenol esters from Euphorbia cornigera
Imam Bakhsh Baloch, Musa Kaleem Baloch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 26ac
C29H37NO7     ÏàËÆ¶È:55.5%
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   Ì¼Æ×Ä£Äâͼ
14 .     compound 27s
C29H40N2O5     ÏàËÆ¶È:55.5%
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   Ì¼Æ×Ä£Äâͼ
15 .     lobarialide C
C29H42O3     ÏàËÆ¶È:55.1%
Chemistry & Biodiversity          2009          6          746-752
Lobarialides A¨CC, Antifungal Triterpenoids from the Lichen Lobaria kurokawae
Xiao-Ning Wang, Hai-Juan Zhang, Dong-Mei Ren, Mei Ji, Wen-Tao Yu, and Hong-Xiang Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 19
C42H57NO4Si     ÏàËÆ¶È:55.1%
Organic Letters          2004          Vol. 6, No. 12          2055-2058
Assignment of Absolute Stereochemistry and Total Synthesis of (-)-Spongidepsin
Arun K. Ghosh and Xiaoming Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     N-Benzyl 3¦Á,7¦Á,24-trimethoxy-12-az¦Á-5¦Â-cholane
C33H53NO3     ÏàËÆ¶È:54.8%
Steroids          2011          76          324-330
Synthesis of 12-oxa, 12-aza and 12-thia cholanetriols
Malika Ibrahim-Ouali, Khalil Hamze, Luc Rocheblave
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     umbellacin D
C23H36O7     ÏàËÆ¶È:53.8%
Journal of Natural Products          2006          69          338-341
Cytotoxic Xenia Diterpenoids from the Soft Coral Xenia umbellata
Ali A. H. El-Gamal, Shang-Kwei Wang, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     daphmanidin A
    ÏàËÆ¶È:53.8%
Journal of Natural Products          2006          69          1065-1069
Daphnioldhanins A−C, Alkaloids from Daphniphyllum oldhami
Shu-Zhen Mu, Ye Wang, Hong-Ping He, Xian-Wen Yang, Yue-Hu Wang, Ying-Tong Di, Yang Lu, Ying Chang, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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