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CCl3D 14.37,19.30,24.85,29.84,32.07,35.05,35.95,47.62,48.08,48.19,52.45,60.90,69.55,101.64,109.18,128.02,142.94,147.76,173.59 |
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lijianfu12: ½ð±Ò+10 2014-10-25 00:06:41
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²éѯ½á¹û£º¹²²éµ½88¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . phanginin G C21H28O5 ÏàËÆ¶È:76.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . phanginin G C21H28O5 ÏàËÆ¶È:76.1% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . phanginin H C21H28O4 ÏàËÆ¶È:71.4% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 7 C16H18O2I2 ÏàËÆ¶È:57.8% Spectrochimica Acta Part A 2005 62 604-613 1H, 13C NMR and X-ray crystallographic studies of highly polyhalogenated derivatives of costunolide lactone D. Corona, E. D¨ªaz, J.L. Nava, A. Guzm¨¢n, H. Barrios, A. Fuentes, S.A. Hernandez-Plata, J. Allard, C.K. Jankowsk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . caesaljapin C21H28O5 ÏàËÆ¶È:57.1% Phytochemistry 1992 31 2897-2898 Caesaljapin, a cassane diterpenoid from Caesalpinia decapetala var. Japonica Kazunori Ogawa, Izumi Aoki, Yutaka Sashida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . curcucomosin A C20H26O3 ÏàËÆ¶È:55% Journal of Natural Products 2010 73 724-728 Labdane Diterpenes from the Aerial Parts of Curcuma comosa Enhance Fetal Hemoglobin Production in an Erythroid Cell Line Ratchanaporn Chokchaisiri, Nattawara Chaneiam, Saovaros Svasti, Suthat Fucharoen, Jim Vadolas and Apichart Suksamrarn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ent-pimaric acid C20H30O2 ÏàËÆ¶È:55% Journal of China Pharmaceutical University 1989 20 203-207 Diterpenes From Pseuduvaria Indochinensis Xie Ning; Zhong Shouming; Zhao Shouxun; Peter G. Waterman; He Cunheng and Zheng Qitai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 36b C22H21NO5 ÏàËÆ¶È:55% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (3'R)-Hydroxystemofoline C22H29NO6 ÏàËÆ¶È:54.5% Journal of Natural Products 2009 72 679-684 Semisynthesis and Biological Activity of Stemofoline Alkaloids Morwenna C.Baird,Stephen G. Pyne, Alison T. Ung, Wilford Lie, Thanapat Sastraruji, Araya Jatisatienr, Chaiwat Jatisatienr, Srisulak Dheeranupattana, Jaturong Lowlam, and Sukanya Boonchalermkit Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . monomethyl ester of caesaljapin ÏàËÆ¶È:54.5% Phytochemistry 1992 31 2897-2898 Caesaljapin, a cassane diterpenoid from Caesalpinia decapetala var. Japonica Kazunori Ogawa, Izumi Aoki, Yutaka Sashida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . dehydroretrofractamide C C20H29NO3 ÏàËÆ¶È:52.6% Phytochemistry 2007 68 899-903 ACAT inhibition of alkamides identified in the fruits of Piper nigrum Mun-Chual Rho, Seung Woong Lee, Hye Ran Park, Jung-Ho Choi, Ji Yun Kang,Koanhoi Kim, Hyun Sun Lee, Young Kook Kim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 16 C17H26O6 ÏàËÆ¶È:52.6% Journal of Natural Products 2005 68 1274-1276 Antifungal Activity of Artemisinin Derivatives Ahmed M. Galal, Samir A. Ross, Melissa Jacob, and Mahmoud A. ElSohly Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3¦Â,7¦Â-dihydroxyandrost-5-en-17-one ÏàËÆ¶È:52.6% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . bryopterin B C17H22O5 ÏàËÆ¶È:52.6% Phytochemistry 1994 37 433-439 Sesqui- and diterpenoids from the panamanian liverwort Bryopteris filicina Fumihiro Nagashima, Hiromi Izumo, Shigeru Takaoka, Motoo Tori, Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ethyl(-)-4-(4'-heptanoyloxyphenyl)-6-methyl-3,4-dihydropyrimidin-2-one-5-carboxylate C21H28N2O5 ÏàËÆ¶È:52.6% Indian Journal of Chemistry Section B 2009 48B 1738-1748 Synthesis and lipase-catalysed enantioselective acylation studies on ethyl 4-aryl-3,4-dihydropyrimidin-2(1H)-ones Prasad,Ashok K; Arya,Pragya; Bhatia,Sumati; Sharma,Raman K; Singh,Rishipal; Singh,Brajendra K; Eycken,Erik Van der; Singh,Rajpal; Olsen,Carl E; Parmar,Virinder S Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . androsta-3,5-dien-17-one ÏàËÆ¶È:52.6% Steroids 1998 63 650-664 The scope and limitations of the reaction of ¦Ä5-steroids with mercury(II) trifluoroacetate Peter L. D. Ruddock, David J. Williams, Paul B. Reese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3¦Â,4¦Â-dihydroxyandrost-5-en-17-one ÏàËÆ¶È:52.6% Steroids 1998 63 650-664 The scope and limitations of the reaction of ¦Ä5-steroids with mercury(II) trifluoroacetate Peter L. D. Ruddock, David J. Williams, Paul B. Reese Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 4¦Â,5¦Â-Epoxyandrostane-6,17-dione ÏàËÆ¶È:52.6% Steroids 1995 60 499-505 Competing pathway involved in allylic acetoxylation of androst-5-en-17-one, and oxidation of allylic alcohols with chromium oxides Mitsuteru Numazawa, Mii Tachibana, Miyako Kamiza Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . androst-3,17-dione-4-eno[6,5,4-c,d]isoxazole C19H23NO3 ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 1998 6 1525-1529 Synthesis of new steroidal isoxazoles: inhibitors of estrogen synthase Shengrong Li, Edward J. Parish, Carla Rodriguez-Valenzuela, Angela M.H. Brodie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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