| ²é¿´: 339 | »Ø¸´: 1 | ||
jintongyxгæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»ÒÑÓÐ1È˲ÎÓë
|
| ÈܼÁ£ºCDCl3 ̼Æ×Êý¾Ý£º15.92,16.15,17.73,18.03,22.93,22.96,23.36,32.58,33.20,39.00,40.99,44.88,49.54,53.76,55.77,56.26,59.39,62.08,63.38,210.72 |
» ²ÂÄãϲ»¶
²©Ê¿¶ÁÍêδÀ´Ò»¶¨»áºÃÂð
ÒѾÓÐ28È˻ظ´
²©Ê¿ÉêÇë¶¼ÊÇÄÚ¶¨µÄÂð£¿
ÒѾÓÐ4È˻ظ´
֮ǰÈÃһ˶ʿÉúË®ÁË7¸ö·¢Ã÷רÀû£¬ÏÖÔÚÕâ7¸ö»ñÅú·¢Ã÷רÀûµÄά»¤·Ñ¿É´ÓÄĶùÖ§³ö¹þ£¿
ÒѾÓÐ3È˻ظ´
µ½Ðµ¥Î»ºó£¬»»ÁËеÄÑо¿·½Ïò£¬Ã»ÓÐÍŶӣ¬³ÖÐø»ýÀÛ2ÇøÒÔÉÏÂÛÎÄ£¬ÄÜÉêÇëµ½ÃæÉÏÂð
ÒѾÓÐ12È˻ظ´
Ͷ¸å¾«Ï¸»¯¹¤
ÒѾÓÐ4È˻ظ´
¸ßÖ°µ¥Î»Í¶¼ÆËã»úÏà¹ØµÄ±±ºË»òSCIËÄÇøÆÚ¿¯ÍƼö£¬ÇóÖ§ÕУ¡
ÒѾÓÐ4È˻ظ´
µ¼Ê¦ÏëÈÃÎÒ´Ó¶ÀÁ¢Ò»×÷±ä³ÉÁ˹²Ò»µÚÒ»
ÒѾÓÐ9È˻ظ´
¶Á²©
ÒѾÓÐ4È˻ظ´
JMPT ÆÚ¿¯Í¶¸åÁ÷³Ì
ÒѾÓÐ4È˻ظ´
ÐÄÂöÊÜËð
ÒѾÓÐ5È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¼±Çó΢Æ× ллY2-3
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
Çó΢Æ×£¬ÏàËÆ¶È80%ÒÔÉϵģ¬Ð»Ð»¸÷λÁË£¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
÷´º
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 242 (´óѧÉú)
- ½ð±Ò: 1940.6
- É¢½ð: 48
- ºì»¨: 3
- Ìû×Ó: 465
- ÔÚÏß: 121.1Сʱ
- ³æºÅ: 1536801
- ×¢²á: 2011-12-14
- ÐÔ±ð: MM
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jintongyx: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-02-28 11:32:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jintongyx: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-02-28 11:32:02
|
1 . 7¦Á,8¦Á,13¦Â,14¦Â-diepoxyabietan-18-oic acid C20H30O4 ÏàËÆ¶È:80% Planta Medica 2001 67 55-60 Abietane Diterpenoids from the Cones of Larix kaempferi and their Inhibitory Effects on Epstein-Barr Virus Activation Hironori Ohtsu, Reiko Tanaka, Yasuko In, Shunyo Matsunaga, Harukuni Tokuda, Hoyoku Nishino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . methyl 7,8(¦Á+¦Â)-epoxy-14-oxolabdan-17-oate C21H34O4 ÏàËÆ¶È:76.1% Molecules 2004 9 300-322 From Labdanes to Drimanes. Degradation of the Side Chain of Dihydrozamoranic Acid. Jes¨²s M. Rodilla, D. D¨ªez, J. G. Urones and Pedro M. Rocha Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . ((1S,2R,4aS,8aS)-5,5,8a-trimethyl-decahydronaphthalene-1,2-diyl)bis(methylene) diacetate C19H32O4 ÏàËÆ¶È:75% Journal of Natural Products 1996 59 866-868 Drimane Sesquiterpenes from the Sponge Dysidea fusca A. Montagnac, M.-T. Martin, C. Debitus, and M. Païs Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (13R, 14R)-8,13-epoxylabdane-14,15-diol ÏàËÆ¶È:75% Planta Medica 1992 58 713 First Diterpenes from Arnica Th. Schmidt, C. M. Pajireiter, D. Wendisch,and C. Willuhn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2¦Â-hydroxy-8,15(R)-oxydo-ent-pimaran C20H34O3 ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 1983 31 4409-4416 Chemische und Chemotaxonomische Untersuchungen der Pterophyten. XLIV. Chemische Untersuchungen der Inhaltsstoffe von Microlepia marginata (PANZER) C. CHR. (2) TADAYUKI KURAISHI,TAKAO TANIGUCHI,KAZUYUKI HORI,TAKAO MURAKAMI,NOBUTOSHI TANAKA,YASUHISA SAIKI and CHIUMING CHEN Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (1S,4R,5R,6R,7S,10R,11S)-4,5-Epoxycadin-12,6-olide-13-ylphosphonic acid diethyl Ester ÏàËÆ¶È:75% Chemistry of Natural Compounds 2002 38 553-556 PHOSPHATE DERIVATIVES OF NATURAL LACTONES.II. SYNTHESIS OF NOVEL DIALKYLPHOSPHONATES OF ARTEANNUIN B R. I. Dzhalmakhanbetova, E. M. Suleimenov, B. B. Rakhimova,N. A. Talzhanov, A. T. Kulyyasov, and S. M. Adekenov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . ent-14¦Â-hydroxykaur-16-en-15-one C20H32O2 ÏàËÆ¶È:75% Phytochemistry 1999 50 423-433 11-O-xygenated cytotoxic 8,9-secokauranes from a New Zealand liverwort, Lepidolaena taylorii Nigel B. Perry, Elaine J. Burgess, Seung-Hwa Baek, Rex T. Weavers, Wolfgang Geis, Anthony B. Mauger Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 13 ÏàËÆ¶È:75% Journal of Natural Products 1984 Vol 47 592-599 Cmr Spectroscopy of Labdanic Diterpenes and Related Substances Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 18d(14-epimer) ÏàËÆ¶È:75% Journal of Natural Products 1984 Vol 47 592-599 Cmr Spectroscopy of Labdanic Diterpenes and Related Substances Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (13R,14R)-8¦Á,13-Epoxylabdan-14,15-diol ÏàËÆ¶È:75% Phytochemistry 1995 40 1213-1218 Diterpenes from Arnica angustifolia Thomas J. Schmidt, Claus M. Passreiter, Detlef Wendisch, G¨¹nter Willuhn Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 4 ÏàËÆ¶È:75% Tetrahedron letters 1982 23 4349-4352 Fern constituent: colysanoxide, and onoceroid having a novel carbon skeleton, isolated from colysis species Hiroyuki Ageta, Kazur Masuda, Masatoshi Inoue, Toshimasa Ishida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . verrucosin-9 ÏàËÆ¶È:75% Tetrahedron 1997 53 1491-1504 Novel verrucosins from the skin of the Mediterranean nudibranch Doris verrucosa Margherita Gavagnin, Nicon Ungur, Francesco Castelluccio, Guido Cimino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . methyl 12a,13a-epoxy-isoanticopal-15-oate C21H34O3 ÏàËÆ¶È:75% Tetrahedron 2007 63 8939-8948 Nor-limonoid and homoisoanticopalane lactones from methyl isoanticopalate Pilar Basabe, Sergio Delgado, Isidro S. Marcos, David Diez, Alberto Diego, M¨®nica de Rom¨¢n, Francisca Sanz, J.G. Urones Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . ent-14¦Á-hydroxy-16-kauren-15-one ÏàËÆ¶È:75% Journal of the Chinese Chemical Society 1997 44 385-389 Kaurane-type Diterpenoids from Liverworts „¢»ÝÈå(Huei-Ju Liu);ÔøÊç»Ý(Shu-Huey Tseng);…ÇÈÊß_(Jen-Dar Wu);…ǼÎû?(Chia-Li Wu) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Â,17,19-Trihydroxyspongia-13(16),14-dien-2-one C20H28O5 ÏàËÆ¶È:75% Australian Journal of Chemistry 1979 32 867-880 A New Series of Diterpenes from Australian Spongia Species R Kazlauskas, PT Murphy, RJ Wells, K Noack, WE Oberhansli and P Schonholzer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â,17,19-Trihydroxyspongia-13(16),14-dien-2-one ÏàËÆ¶È:75% The Journal of Organic Chemistry 1991 56 1250-1253 New spongian diterpenoids from a great barrier reef sponge, Spongia sp Sarath P. Gunasekera, Francis J. Schmitz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . ent-7¦Á-acetoxy-17-hydroxy-15¦Á,16¦Á-epoxybeyeran-12-one C22H32O5 ÏàËÆ¶È:72.7% Journal of Natural Products 1997 60 86-92 Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . mansumbinone epoxide C22H34O2 ÏàËÆ¶È:72.7% Phytochemistry 1986 25 917-922 The mansumbinanes: Octanordammaranes from the resin of Commiphora incisa Gordon J. Provan, Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . isoagathenediol monoacetate ÏàËÆ¶È:72.7% Microbiology 1995 141 2659-2663 The isolation of isoagathenediol: a new tricyclic diterpene from the lipids of Rhodospirillum rubrum Jo-Anne Chuck and Kevin D. Barrow Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . methyl 7,8(¦Á)epoxy-15-hydroxylabdan-17-oate C21H36O4 ÏàËÆ¶È:71.4% Molecules 2004 9 300-322 From Labdanes to Drimanes. Degradation of the Side Chain of Dihydrozamoranic Acid. Jes¨²s M. Rodilla, D. D¨ªez, J. G. Urones and Pedro M. Rocha |
2Â¥2015-02-28 11:16:34












»Ø¸´´ËÂ¥