| ²é¿´: 1927 | »Ø¸´: 7 | |||
Ñî´óËÉÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
|
|
̼Æ×Êý¾ÝÈçÏ£º 16.4,19.5,20.1,20.3,23.7,24.4,26.5,28.1,28.6,41.1,44.4,48.4,56.3,75.1,80.4 ÐÁ¿à¸÷λÁË£¬·Ç³£¸Ðл¡£ |
» ±¾ÌûÒÑ»ñµÃµÄºì»¨£¨×îÐÂ10¶ä£©
» ²ÂÄãϲ»¶
Çóµ÷¼ÁԺУÐÅÏ¢
ÒѾÓÐ4È˻ظ´
085600²ÄÁÏÓ뻯¹¤306
ÒѾÓÐ4È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
328Çóµ÷¼Á£¬Ó¢ÓïÁù¼¶551£¬ÓпÆÑоÀú
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ070300 ѧ˶336Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
286·ÖÈ˹¤ÖÇÄÜרҵÇëÇóµ÷¼ÁÔ¸Òâ¿ç¿¼£¡
ÒѾÓÐ8È˻ظ´
×ÊÔ´Óë»·¾³ µ÷¼ÁÉêÇë(333·Ö)
ÒѾÓÐ5È˻ظ´
280Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
269ר˶Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
²ÄÁÏѧ˶301·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
ÇóÖú3¸öÓÃ΢Æ×½âÎöµÄ½á¹¹
ÒѾÓÐ8È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÔÚexcelÀï´¦ÀíÒ»ÏÂÊý¾ÝÇó΢·Ö£¬Çë¸ßÊÖÖ¸½ÌÒ»ÏÂ~ллÀ²~
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿Î¢·´-É«Æ× ÔõôʹÓ𡣿
ÒѾÓÐ8È˻ظ´

|
2Â¥2012-10-06 13:53:04
wangfei.ac
Ìú¸Ëľ³æ (ÕýʽдÊÖ)
- PhEPI: 1
- Ó¦Öú: 391 (˶ʿ)
- ½ð±Ò: 5988.3
- É¢½ð: 382
- ºì»¨: 18
- Ìû×Ó: 947
- ÔÚÏß: 321Сʱ
- ³æºÅ: 1505634
- ×¢²á: 2011-11-23
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2012-10-06 15:50:53
Ñî´óËÉ
ÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
- Ó¦Öú: 243 (´óѧÉú)
- ½ð±Ò: 23878.3
- É¢½ð: 3
- ºì»¨: 46
- Ìû×Ó: 10466
- ÔÚÏß: 831.8Сʱ
- ³æºÅ: 1190374
- ×¢²á: 2011-01-15
- רҵ: »¯Ñ§ÉúÎïѧÓëÉúÎïÓлú»¯Ñ§

4Â¥2012-10-06 16:36:11
»ð¼ý´©Æ¨Æ¨
ľ³æ (ÕýʽдÊÖ)
µØÇòÇò³¤
- Ó¦Öú: 197 (¸ßÖÐÉú)
- ½ð±Ò: 3684.8
- ºì»¨: 8
- Ìû×Ó: 529
- ÔÚÏß: 194.4Сʱ
- ³æºÅ: 407719
- ×¢²á: 2007-06-20
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ

5Â¥2012-10-07 08:30:38
Ñî´óËÉ
ÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
- Ó¦Öú: 243 (´óѧÉú)
- ½ð±Ò: 23878.3
- É¢½ð: 3
- ºì»¨: 46
- Ìû×Ó: 10466
- ÔÚÏß: 831.8Сʱ
- ³æºÅ: 1190374
- ×¢²á: 2011-01-15
- רҵ: »¯Ñ§ÉúÎïѧÓëÉúÎïÓлú»¯Ñ§

6Â¥2012-10-07 09:40:48
»ð¼ý´©Æ¨Æ¨
ľ³æ (ÕýʽдÊÖ)
µØÇòÇò³¤
- Ó¦Öú: 197 (¸ßÖÐÉú)
- ½ð±Ò: 3684.8
- ºì»¨: 8
- Ìû×Ó: 529
- ÔÚÏß: 194.4Сʱ
- ³æºÅ: 407719
- ×¢²á: 2007-06-20
- ÐÔ±ð: GG
- רҵ: ÌìȻҩÎﻯѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
Ñî´óËÉ: ½ð±Ò+25, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-10-08 07:55:53
Ñî´óËÉ: ½ð±Ò+25, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-10-08 07:55:53
|
²éѯ½á¹û£º¹²²éµ½561¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . acomadendrane-4¦Â,10¦Â-diol C15H26O2 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 2000 48(3) 357-361 The Constituents of the Root and Stem of Aristolochia heterophylla Hemsl Tian-Shung Wu ,Yu-Yi CHAN ,and Yann-Lii LEU Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . D-aromadendrane-4¦Â, 10¦Á-diol C15H26O2 ÏàËÆ¶È:100% Acta Botanica Yunnanica 2002 24(1) 129-132 Sesquiterpenoids from Michelia lacei and Their Chemotaxonomic Significance CHENG Yong-Xian,LEI Mao-Lin,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 4¦Â,10¦Á-aromadendranediol C15H26O2 ÏàËÆ¶È:100% Chemical & Pharmaceutical Bulletin 1989 37 509-510 Studies on the Sequiterpenoids of Panax ginseng C. A. MEYER. III Hisakatsu IWABUCHI,Masahiro YOSHIKURA and Wasuke KAMISAKO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 4¦Â,10¦Â-Aromadendranediol ÏàËÆ¶È:100% Journal of Chinese Pharmaceutical Sciences 2009 18 146-150 Chemical constituents isolated from Saruma henryi Shi-Wen Dong; Ming-Ying Shang; Xuan Wang; Shu-Xiang Zhang; Chen Li; Shao-Qing Cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 4¦Á,7¦Á-Aromodendranediol C15H26O2 ÏàËÆ¶È:100% Journal of Asian Natural Products Research 2003 5 215-221 THE CHEMICAL CONSTITUENTS OF MUNRONIA HENRYI SHU-HUA QI, DA-GANG WU, YUN-BAO MA and XIAO-DONG LUO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ent-4¦Â10¦Á-dihydroxyaromadendrane C15H26O2 ÏàËÆ¶È:100% Phytochemistry 1994 36 1425-1430 Sesqui- and diterpenoids from Plagiochila species Fumihiro Nagashima, Hironao Tanaka, Masao Toyota, Toshihiro Hashimoto, Yukiko Kan, Shigeru Takaoka, Motto Tori, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 13 ÏàËÆ¶È:100% Phytochemistry 1987 26 1059-1063 Sesquiterpene lactones and a sesquiterpene diol from jamaican ambrosia peruviana Gwendolyn Goldsby,Basil A. Burke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ent-4¦Á,10¦Â-dihydroxyaromaden-drane ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2007 38 656-659 Chemical constituents from fruits of Vitex trifolia GU Qiong; ZHANG Xue-mei; JIANG Zhi-yong; CHEN Ji-jun; ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 4¦Â,7¦Á-aromadendranedio ÏàËÆ¶È:100% Chinese Traditional and Herbal Drugs 2001 32 778-780 Studies on chemical constituents of Cipadessa baccifera LUO Xiao dong; WU Shao hua; MA Yun bao; WU Da gang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 4¦Â,10¦Á-aromadendranediol ÏàËÆ¶È:100% Chinese Journal of Natural Medicines 2003 1 193-195 Studies on the Chemical Constituents of the Soft Coral Sinularia sp JIA Rui; GUO Yue-Wei; HOU Hui-Xin; Mollo Ernes to; Cimino Guido Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 4¦Â,10¦Á-aromadendranediol C15H26O2 ÏàËÆ¶È:100% Tetrahedron 1995 51 10997-11010 Terpenoid and steroid constituents of the Indian ocean soft coral Sinularia maxima Ammanamanchi S.R. Anjaneyulu, Kadali S. Sagar, Mukku J.R.V. Venugopal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (-)-4¦Â,7¦Á-aromadendranediol ÏàËÆ¶È:100% Journal of the Chinese Chemical Society 2000 47 1291-1293 Sesquiterpenes from Ligularia fischeri Wen-Shu Wang, Qi-Xiu Zhu,Kun Gao and Zhong-Jian Jia* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 4¦Á,10¦Â-aromadendranediol ÏàËÆ¶È:100% Journal of Chemical Research 2007 31 310-312 Two new sesquiterpenoids from Doellingeria scaber Bai, Suping; Xingke,; Lu, Guangzhou; Yan, Fulin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . syriacine C15H26O2 ÏàËÆ¶È:100% Journal of Asian Natural Products Research 2012 14 618-625 New terpenes from Salvia palaestina Benth. and Salvia syriaca L. growing wild in Jordan Hala I. Al-Jaber, Khadeja K. Abrouni, Mahmuod A. Al-Qudah & Musa H. Abu Zarga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (+)-3¦Á,9¦Â-aromaden-dranediol ÏàËÆ¶È:100% Chinese Journal of Organic Chemistry 2004 24 806-810 Sesquiterpenes from Caragana Intermedia SUN, Zhi-Hua ZHANG, Su SHI, Jiao HU, Chang-Qi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . aromadendrane-4¦Â,10¦Á-diol ÏàËÆ¶È:100% Journal of the Brazilian Chemical Society 2003 14 828-813 Antifungal Aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis Isabel C. Moreira, João Henrique G. Lago, Maria Cl¨¢udia M. Young and N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 10 ÏàËÆ¶È:86.6% Phytochemistry 1987 26 1059-1063 Sesquiterpene lactones and a sesquiterpene diol from jamaican ambrosia peruviana Gwendolyn Goldsby,Basil A. Burke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 4¦Á,10¦Á-aromadendranediol C15H26O2 ÏàËÆ¶È:86.6% Natural Product Research and Development 2005 17 740-745 Chemical Studies on Sesquiterpenes in Soft Coral Lobophytum sp. from the South China Sea ZHANG Wen; GUO Yue-wei *; MOLLO Ernesto; CIMINO Guido Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . aromadendrane-4¦Á,10¦Á-diol ÏàËÆ¶È:86.6% Journal of the Brazilian Chemical Society 2003 14 828-813 Antifungal Aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis Isabel C. Moreira, João Henrique G. Lago, Maria Cl¨¢udia M. Young and N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . aromadendrane-4¦Â,10¦Á,15-triol C15H26O3 ÏàËÆ¶È:80% Journal of the Brazilian Chemical Society 2003 14 828-813 Antifungal Aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis Isabel C. Moreira, João Henrique G. Lago, Maria Cl¨¢udia M. Young and N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 5-Acetoxy-aromadendrane-4¦Â,10¦Á-diol ÏàËÆ¶È:76.4% Journal of the Brazilian Chemical Society 2003 14 828-813 Antifungal Aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis Isabel C. Moreira, João Henrique G. Lago, Maria Cl¨¢udia M. Young and N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . pipelol A C15H26O3 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2002 50(10) 1413-1415 New Megastigmane Glycoside and Aromadendrane Derivative from the Aerial Part of Piper elongatum Chikako MASUOKA,Masateru ONO, Yasuyuki ITO,Masafumi OKAWA,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 14-endohydroxyglobulol C15H26O2 ÏàËÆ¶È:73.3% Phytochemistry 1992 31 3749-3755 Microbial oxidation of tricyclic sesquiterpenoids containing a dimethylcyclopropane ring Wolf-Rainer Abraham, Klaus Kieslich, Burkhard Stumpf, Ludger Ernst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 4¦Â,10¦Á,15-trihydroxyaromadrendane ÏàËÆ¶È:73.3% Chinese Journal of Natural Medicines 2009 7 270-273 Two New Terpenoids from Valeriana officinalis ZHOU Ying; FANG Ying; GONG Zhan-Feng; DUAN Xue-Yun; LIU Yan-Wen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . ent-4¦Â-Hydroxy-10¦Á-methoxyaromadendrane ÏàËÆ¶È:68.7% Phytochemistry 2000 53 845-849 Sesquiterpenoids and diterpenoids from the Chilean liverwort Lepicolea ochroleuca Huei-Ju Liu, Chia-Li Wu, Hans Becker, Josef Zapp Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 4-¦Â-hydroxy-10¦Á-methoxyaromadendrane ÏàËÆ¶È:68.7% Tetrahedron 1997 53 9301-9312 Rare aromadendrane diterpenoids from a new soft coral species of Sinularia genus of the Indian Ocean Ammanamanchi S.R. Anjaneyulu, Moturu V.R. Krishnamurthy, Gottumukkala V. Rao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 4¦Â,10¦Á-aromadendranediol-10-methylether C16H28O2 ÏàËÆ¶È:68.7% Tetrahedron 1995 51 10997-11010 Terpenoid and steroid constituents of the Indian ocean soft coral Sinularia maxima Ammanamanchi S.R. Anjaneyulu, Kadali S. Sagar, Mukku J.R.V. Venugopal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . 4¦Á-hydroxy-10¦Â-methoxy-aromadendrane ÏàËÆ¶È:68.7% Journal of Chemical Research 2007 31 310-312 Two new sesquiterpenoids from Doellingeria scaber Bai, Suping; Xingke,; Lu, Guangzhou; Yan, Fulin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . compound 4 C15H26O3 ÏàËÆ¶È:66.6% Journal of Natural Products 2006 69 1411-1416 Cytotoxic Constituents from the Formosan Soft Coral Clavularia inflata var. luzoniana Shang-Kwei Wang, Min-Jay Huang, and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . comound 4 C14H22O ÏàËÆ¶È:66.6% Journal of Natural Products 2004 67 577-583 New Marine Sesquiterpenoids and Diterpenoids from the Okinawan Soft Coral Clavularia koellikeri Kazuo Iguchi, Takashi Fukaya, Akiko Yasumoto, and Kinzo Watanabe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . patchoulol ÏàËÆ¶È:66.6% Journal of Natural Products 1999 62 437-440 Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . (9R)-9-hydroxypatchoulol C15H26O2 ÏàËÆ¶È:66.6% Journal of Natural Products 1999 62 437-440 Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 10-aromadendranol ÏàËÆ¶È:66.6% Planta Medica 1995 61 196-197 Isolation and Identification of 11- Selinen-4¦Á,7¦Â-ol and 10-Aromadendranolin the Essential Oil of Murraya koenigii I. Wa¦Âmuth- Wagner, H.-O. Kalinowski. andH. fork Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . globulol C15H26O ÏàËÆ¶È:66.6% Acta Bot. Boreal. -Occident. Sin. 2006 26 2146-2149 Liposoluble Constituents in Eucalyptus globulus Labill. Fruits TAN MAN-Liang, WANG Ye, ZHOU Li-gang, JIANG Wei-bo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . globulol ÏàËÆ¶È:66.6% Natural Product Research 2008 22 569-575 Antimicrobial activity of globulol isolated from the fruits of Eucalyptus globulus Labill Manliang Tan; Ligang Zhou; Yongfu Huang; Ye Wang; Xiaojiang Hao; Jingguo Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . patchoulol ÏàËÆ¶È:66.6% Phytochemistry 1999 52 635-638 The microbiological hydroxylation of the sesquiterpenoid patchoulol by Mucor plumbeus Simone Fontes Arantes, James R. Hanson, Peter B. Hitchcock Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . patchouli alcohol ÏàËÆ¶È:66.6% Phytochemistry 1995 39 713-714 Sesquiterpenoids from Valeriana fauriei Koichi Nishiya, Tsuyoshi Tsyjiyama, Takefumi Kimura, Koichi Takeya, Hideji Itokawa, Yoichi Iitaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . patchouli alcohol ÏàËÆ¶È:66.6% Phytochemistry 1995 39 713-714 Sesquiterpenoids from Valeriana fauriei Koichi Nishiya, Tsuyoshi Tsyjiyama, Takefumi Kimura, Koichi Takeya, Hideji Itokawa, Yoichi Iitaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . globulol C15H26O2 ÏàËÆ¶È:66.6% Phytochemistry 1994 37 1023-1025 The hydroxylation of globulol and 7-epiglobulol by Cephalosporium aphidicola James R. Hanson, Peter B. Hitchcock, Revathy Manickavasagar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . (-)-globulol ÏàËÆ¶È:66.6% Phytochemistry 1994 37 1027-1030 Biotransformation of sesquiterpenoids, (− -globulol and (+)-ledol by Glomerella cingulataMitsuo Miyazawa, Tomoaki Uemura, Hiromu Kameoka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . globulol ÏàËÆ¶È:66.6% Phytochemistry 1992 31 3749-3755 Microbial oxidation of tricyclic sesquiterpenoids containing a dimethylcyclopropane ring Wolf-Rainer Abraham, Klaus Kieslich, Burkhard Stumpf, Ludger Ernst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . patchouli alcohol ÏàËÆ¶È:66.6% Korean Journal of Pharmacognosy 1998 29(1) 18-21 Isolation and Quantitative Determination of Patchouli alcohol from Pogostemon cablin Benth. Kim, Ju-Sun; Chi, Hyung-Joon; Won, Do-Hee; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . compound 12 ÏàËÆ¶È:66.6% Phytochemistry 1987 26 1059-1063 Sesquiterpene lactones and a sesquiterpene diol from jamaican ambrosia peruviana Gwendolyn Goldsby,Basil A. Burke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . 4,7,8-Eudesmatriol C15H28O3 ÏàËÆ¶È:66.6% Natural Product Research 2010 24 687-696 Terpenes and flavonoids from an Egyptian collection of Cleome droserifolia Mohamed I. Aboushoer; Hoda M. Fathy; Maged S. Abdel-Kader; Gilles Goetz; Abdallah A. Omar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . (+)-globulol C15H26O ÏàËÆ¶È:66.6% Russian Chemical Bulletin 1999 48 600-603 (+)-Globulol as a new sesquiterpene alcohol fromAngelica sylvestris L. E. Yu. Vinokurova, E. E. Shults, I. Yu. Bagryanskaya, Yu. V. Gatilov and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . (-)-globulol C15H26O ÏàËÆ¶È:66.6% Russian Chemical Bulletin 1999 48 600-603 (+)-Globulol as a new sesquiterpene alcohol fromAngelica sylvestris L. E. Yu. Vinokurova, E. E. Shults, I. Yu. Bagryanskaya, Yu. V. Gatilov and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . 7¦Á-hydroxyaromadendrane ÏàËÆ¶È:66.6% Journal of Chemical Research 1997 21 28-29 Hydroxylation of Aromadendrane Derivatives by Mucor plumbeus† Ricardo Guillermo, James R. Hanson and Almaz Truneh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . (-)-globulol C15H26O ÏàËÆ¶È:66.6% Journal of the Brazilian Chemical Society 1990 1 105-109 Composition of the Essential Oil of Vassoura. Carmen Lucia Queiroga, Alberto Fukai and Anita J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . (-)-4¦Â,7¦Â-aromadendranediol C15H26O2 ÏàËÆ¶È:66.6% Journal of the Brazilian Chemical Society 1990 1 105-109 Composition of the Essential Oil of Vassoura. Carmen Lucia Queiroga, Alberto Fukai and Anita J. Marsaioli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . Hiiranlactone G C15H24O2 ÏàËÆ¶È:66.6% Phytochemistry 2011 72 415-422 Secondary metabolites from the leaves of Neolitsea hiiranensis and the anti-inflammatory activity of some of them Bi-Jiuan Liou, Hsun-Shuo Chang, Guei-Jane Wang, Michael Y. Chiang, Chang-Hui Liao, Chu-Hung Lin, Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . aromadendrane-4¦Â,10¦Â-diol ÏàËÆ¶È:66.6% Journal of the Brazilian Chemical Society 2003 14 828-813 Antifungal Aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis Isabel C. Moreira, João Henrique G. Lago, Maria Cl¨¢udia M. Young and N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 52 . 16¦Á-hydroxy-(-)-kauran-19-oic acid C20H32O2 ÏàËÆ¶È:63.1% China Journal of Chinese Materia Medica 1989 14 38-40 Studies on the Chemcial Constituents of the Roots of Aralia continetalis Kitag Wang Guangshu, Shao Chunjie and Xu Jingda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 53 . deacetylfawcettiine ÏàËÆ¶È:62.5% Tetrahedron 2005 61 3681-3690 Lannotinidines A¨CG, new alkaloids from two species of Lycopodium Koichiro Koyama, Hiroshi Morita, Yusuke Hirasawa, Miwa Yoshinaga, Tomohiro Hoshino, Yutaro Obara, Norimichi Nakahata, Jun'ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 54 . (¡À)-3¦Á-acetoxy-14-oxo-4¦Á,4¦Â,10¦Á-trimethyl-1,2,3,4,5¦Â,6,7,8¦Á,9¦Â,10,11,12,13,14-perhydrophenanthrene C19H30O3 ÏàËÆ¶È:61.1% Tetrahedron 1985 41 5653-5660 Synthesis of oryzalexins a, b and c, the diterpenoidal phytoalexins isolated from rice blast leaves infected with pyricularia oryzae Kenji Mori, Michiru Waku Structure 13C NMR ̼Æ×Ä£Äâͼ |

7Â¥2012-10-08 07:47:15
Ñî´óËÉ
ÖÁ×ðľ³æ (ÎÄ̳¾«Ó¢)
- Ó¦Öú: 243 (´óѧÉú)
- ½ð±Ò: 23878.3
- É¢½ð: 3
- ºì»¨: 46
- Ìû×Ó: 10466
- ÔÚÏß: 831.8Сʱ
- ³æºÅ: 1190374
- ×¢²á: 2011-01-15
- רҵ: »¯Ñ§ÉúÎïѧÓëÉúÎïÓлú»¯Ñ§

8Â¥2012-10-08 07:56:19













»Ø¸´´ËÂ¥
Ñî´óËÉ
-globulol and (+)-ledol by Glomerella cingulata