| ²é¿´: 652 | »Ø¸´: 4 | ||||
WJY515Ìú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóάÆÕÊý¾Ý
|
|
ÇóάÆÕ Êý¾ÝÈçÏÂ: 19.3 19.8 20.3 21.1 21.1 21.2 22.3 24.0 24.3 28.0 29.8 34.2 37.8 42.5 43.2 43.9 49.2 61.6 68.3 74.0 76.6 83.5 113.4 141.7 170.2 170.3 170.6 171.0 лл |
» ²ÂÄãϲ»¶
284Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
±¾¿ÆÉúÎïÐÅϢѧ£¬×Ü·Ö362 Çó07 08µ÷¼Á
ÒѾÓÐ3È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
333Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ7È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
312Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085602»¯Ñ§¹¤³Ì268·Ö¶×µ÷¼Á
ÒѾÓÐ9È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
WJY515: ½ð±Ò+2, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-23 13:12:47
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
WJY515: ½ð±Ò+2, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-23 13:12:47
|
¸ñʽ²»¶ÔŶ ²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 |

2Â¥2013-10-22 21:01:20
WJY515
Ìú³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 1669.8
- Ìû×Ó: 69
- ÔÚÏß: 58.1Сʱ
- ³æºÅ: 2398609
- ×¢²á: 2013-04-03
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2013-10-23 13:12:05
WJY515
Ìú³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 1669.8
- Ìû×Ó: 69
- ÔÚÏß: 58.1Сʱ
- ³æºÅ: 2398609
- ×¢²á: 2013-04-03
- רҵ: ÌìȻҩÎﻯѧ
4Â¥2013-10-23 13:42:47
danil1288
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 96 (³õÖÐÉú)
- ½ð±Ò: 4099.5
- É¢½ð: 14
- ºì»¨: 2
- Ìû×Ó: 405
- ÔÚÏß: 109.3Сʱ
- ³æºÅ: 779961
- ×¢²á: 2009-05-26
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©Ò©ÐÔÀíÂÛ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
WJY515: ½ð±Ò+3, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-28 14:31:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
WJY515: ½ð±Ò+3, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-10-28 14:31:59
|
²éѯ½á¹û£º¹²²éµ½1467¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3-[(3S,5R,6S,9R)-6-Isopropyl-1,9-dimethyl-1,4-diazaspiro[4.5]decan-2-one-3-yl]-(2S)-2-hydroxypropyl 1-thio-2,3,4,6-tetra-O-acetyl-¦Â-D-glucopyranoside C30H48N2O11S ÏàËÆ¶È:70% Tetrahedron 2012 68 1762-1768 Cycloaddition of a chiral nitrone to allylic motifs: an access to enantiopure sugar-based amino acids displaying a stable glycosidic bond and to 4(S)-4-hydroxy-l-ornithine Kaïss Aouadi, Moncef Msaddek, Jean-Pierre Praly Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (2S,3S,4R,5R,7S,8R,13R,15R)-3,5,7,8,15-pentaacetoxy-9,14-dioxojatropha-6(17),11E-diene C30H40O12 ÏàËÆ¶È:68.9% Chinese Chemical Letters 2006 17 201-203 A New Jatrophane Diterpenoid Ester from Euphorbia turczaninowii Li Gen LIU, Ren Xiang TAN, You Ming GONG Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . milolide H C28H40O12 ÏàËÆ¶È:67.8% Journal of Natural Products 2002 65 704-708 Milolides G-N, New Briarane Diterpenoids from the Western Pacific Octocoral Briareum stechei Jong Hwan Kwak,Francis J. Schmitz, and Gary C. Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1¦Á,7¦Á,14¦Á,18-tetraacetoxy-8,15-isopimaradiene C28H40O8 ÏàËÆ¶È:67.8% Tetrahedron 1999 55 7375-7388 Diterpenoids from Lycopus europaeus and Nepeta septemcrenata: Revised structures and new isopimarane derivatives Ahmed A. Hussein, Benjam¨ªn Rodr¨ªguez, Mar¨ªa de la Paz Mart¨ªnez-Alc¨¢zar, F¨¦lix H. Cano Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ptychantin I ÏàËÆ¶È:67.8% Journal of the Chinese Chemical Society 2001 48 241-247 Ptychantins from the Liverwort Ptychanthus striatus Chia-Li Wu*, Chien-Jen Wang and Ming-Horng Yin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . S-[(1S,2S,2'S,3'aS,5R)-2-Isopropyl-5,50-dimethyl-3',3'a-dihydro-2'H-spiro[cyclohexane-1,6'-imidazo[1,5-b]isoxazol]-4'(5'H)-one-2'-yl]-methyl 1-thio-2,3,4,6-tetra-O-acetyl-¦Â-D-glucopyranoside C30H46N2O11S ÏàËÆ¶È:66.6% Tetrahedron 2012 68 1762-1768 Cycloaddition of a chiral nitrone to allylic motifs: an access to enantiopure sugar-based amino acids displaying a stable glycosidic bond and to 4(S)-4-hydroxy-l-ornithine Kaïss Aouadi, Moncef Msaddek, Jean-Pierre Praly Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ptychantin N ÏàËÆ¶È:66.6% Journal of the Chinese Chemical Society 2001 48 241-247 Ptychantins from the Liverwort Ptychanthus striatus Chia-Li Wu*, Chien-Jen Wang and Ming-Horng Yin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Alangionoside E pentaacetate ÏàËÆ¶È:65.5% Phytochemistry 1995 38 1431-1435 Alangionosides C---F, megastigmane glycosides from Alangium premnifolium Hideaki Otsuka, Kenji Kamada, Masami Yao, Kaori Yuasa, Ikuko Kida, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 1a ÏàËÆ¶È:64.5% Phytochemistry 1998 47 63-68 Sesquiterpene glycosides from Dictamnus dasycarpus Weimin Zhao, Jean-Luc Wolfender, Kurt Hostettmann, Hong-Yu Li, Helen Stoeckli-Evans, Rensheng Xu, Guowei Qin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . agallochaol F ÏàËÆ¶È:64.2% Helvetica Chimica Acta 2005 Vol. 88 979 Secoatisane- and Isopimarane-Type Diterpenoids from the Chinese Mangrove Excoecaria agallocha L. Ji-Dong Wang, Zhen-Yu Li, Yue-Wei Guo Structure 13C NMR ̼Æ×Ä£Äâͼ |

5Â¥2013-10-23 14:18:42














»Ø¸´´ËÂ¥