| ²é¿´: 232 | »Ø¸´: 1 | |||
°²°²anan_tbгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
¼±£¡Çó΢Æ×½âÎö ÒÑÓÐ1È˲ÎÓë
|
|
YB-8 ÈܼÁ£ºÂȷ ̼Æ×Êý¾Ý£º9.81,10.54,10.89,13.07,14.16,23.75,26.65,29.21,40.41,45.22,49.95,52.38,61.06,73.04,75.70, 85.54,105.26,122.57,123.49,125.93,130.77,135.82,151.03,164.49,167.77,171.04,171.57, 172.04,174.27,175.84 |
» ²ÂÄãϲ»¶
080100Á¦Ñ§316Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ13È˻ظ´
Ò»Ö¾Ô¸Î÷±±¹¤Òµ´óѧ289 085602
ÒѾÓÐ3È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ20È˻ظ´
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ26È˻ظ´
¿¼ÑжþÂÖµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϸ´ÊÔÇóµ÷¼Á
ÒѾÓÐ17È˻ظ´
085601³õÊÔ330·ÖÕÒµ÷¼Á
ÒѾÓÐ9È˻ظ´
291 Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ17È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
EPR½âÆ×ÎÊÌ⣬Çó
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
Çó½âºË´ÅÇâÆ×£¡£¡£¡¶àл¶àл£¡£¡
ÒѾÓÐ19È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
ʲôÆ×ͼÄÜÈ·ÈÏ»¯ºÏÎïµÄ½á¹¹
ÒѾÓÐ9È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
Çó΢Æ×£¬ÏàËÆ¶È80%ÒÔÉϵģ¬Ð»Ð»¸÷λÁË£¡£¡
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖúÓÃCDÆ×½âÎöÒ»¸öÄ¾Ö¬ËØÀ໯ºÏÎïµÄ¾ø¶Ô¹¹ÐÍ
ÒѾÓÐ7È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×²é½á¹¹ лл
ÒѾÓÐ3È˻ظ´
Çó΢Æ×Êý¾Ý¿â¼ìË÷2¸öÎå»·ÈýÝÆ»¯ºÏÎï
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
°²°²anan_tb: ½ð±Ò+5, ¡ïÓаïÖú 2015-05-12 09:39:18
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
°²°²anan_tb: ½ð±Ò+5, ¡ïÓаïÖú 2015-05-12 09:39:18
|
1 . spicachlorantin H C31H34O7 ÏàËÆ¶È:54.8% Chemical & Pharmaceutical Bulletin 2011 59(10) 1281-1284 Spicachlorantins G-J, New Lindenane Sesquiterpenoid Dimers from the Roots of Chloranthus spicatus Sang-Yong KIM, Yoshiki KASHIWADA, Kazuyoshi KAWAZOE, Kotaro MURAKAMI, Han-Dong SUN, Shun-Lin LI, and Yoshihisa TAKAISHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . henriol B C35H40O11 ÏàËÆ¶È:51.4% Phytochemistry 2008 69 2867-2874 Bis-sesquiterpenes and diterpenes from Chloranthus henryi Chuang-Jun Li, Dong-Ming Zhang, Yong-Ming Luo, Shi-Shan Yu, Yan Li, Yang Lu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . chloramultilide D C35H40O11 ÏàËÆ¶È:51.4% Journal of Natural Products 2007 70 1987-1990 Mono- and Di-sesquiterpenoids from Chloranthus spicatus Yong-Jiang Xu,Chun-Ping Tang, Chang-Qiang Ke, Ji-Bao Zhang, Hans-Christoph Weiss,Ernst-Rudolf Gesing,and Yang Ye Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . dehydrobruceantinol ÏàËÆ¶È:50% Journal of Natural Products 1995 Vol 58 1915-1919 Bruceanols G and H, Cytotoxic Quassinoids from Brucea antidysenterica Kazumori Imamura, Narihiko Fukamiya, Megumi Nakamura, Masayoshi Okano, Kiyoshi Tagahara, Kuo-Hsiung Lee Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (1Z,2S,3R,4S,6S,7S)-1-ethylidene-7-nitrobenzoyloxy-2,4,6-trimeth-yl-5-oxo-3-[(1S)-1-phenylethoxy]octyl isobutyrate C32H41NO8 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2011 3317-3328 Efficient Asymmetric Synthesis of Long-Chain Polyketides Containing up to Ten Contiguous Stereogenic Centres by Double Chain Elongation Maris Turks, Kelly A. Fairweather, Rosario Scopelliti and Pierre Vogel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-05-11 22:18:10













»Ø¸´´ËÂ¥