| ²é¿´: 312 | »Ø¸´: 1 | ||
xicaicai1988½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖúÒ»¸ö»¯ºÏÎï ÒÑÓÐ1È˲ÎÓë
|
| ̼Æ×Êý¾Ý£º207.847,174.872,134.877,129.542,86.489,77.821,71.81,67.513,53.632,52.815,48.617,20.857,20.786,19.189,15.646 |
» ²ÂÄãϲ»¶
302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601
ÒѾÓÐ5È˻ظ´
²ÄÁÏÓ뻯¹¤371Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
313Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì302·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ4È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ8È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çó
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÒ»¸ö»¯ºÏÎïµÄÌìȻҩÎï·½ÃæµÄÎÄÏ×
ÒѾÓÐ6È˻ظ´
Èç¹ûÎÒÏë²éÒ»¸ö»¯ºÏÎïÔõôºÏ³É£¬ÎÒ¸ÃÔõô²éÎÄÏ×£¿Ð»Ð»
ÒѾÓÐ7È˻ظ´
²éÒ»¸ö»¯ºÏÎïºÏ³É·½·¨µÄÎÊÌâ
ÒѾÓÐ7È˻ظ´
ÇóÖúÒ»¸ö½á¹¹Ê½ÃüÃûµÄÖÐÎÄ·Òë
ÒѾÓÐ7È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
л¯ºÏÎïµ¥¾§Ò»¸öÊý¾Ý»¹¿ÉÒÔ£¬Ã»ÓбðµÄ»òÐíµÈÊý¾Ý£¬¿ÉÒÔͶʲôÔÓ־Ĩ
ÒѾÓÐ16È˻ظ´
Ò»¸ö»¯ºÏÎï¿ÉÒÔÓÐÁ½¸öCASºÅô
ÒѾÓÐ11È˻ظ´
Ò»¸ö»¯ºÏÎïµÄºÏ³É·½·¨
ÒѾÓÐ15È˻ظ´
ÈçºÎÈ·¶¨Ò»¸ö»¯ºÏÎïÊÇÐµģ¬±ðÈËû×ö¹ýºÍ·¢±íµÄ
ÒѾÓÐ14È˻ظ´
Çó²éÒ»¸ö»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú»¯ºÏÎïÃüÃû
ÒѾÓÐ6È˻ظ´
ÓÐûÓÐÒ»¸ö¿ÉÒÔ²éѯ»¯ºÏÎï±ê׼ͼÆ×µÄÍøÕ¾°¡£¿
ÒѾÓÐ4È˻ظ´
ÈçºÎ¸øÓлú»¯ºÏÎï×¢²áÒ»¸öеÄCASºÅ
ÒѾÓÐ7È˻ظ´
ÇóÖú½âÎöÒ»»¯ºÏÎïµÄHÆ×CÆ×£¬¸½ÉÏͼÆ×
ÒѾÓÐ13È˻ظ´
ÔõÑùÖªµÀÒ»¸ö»¯ºÏÎïµÄ¼«ÐÔ
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿¸÷λºÃ£¬ÇëÎÒ¿´Ò»¸ö¼òµ¥»¯ºÏÎïµÄHNMRÆ×ͼ¡£
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ²éµ½Ò»¸öÒÑÖª»¯ºÏÎïµÄ¾§Ìå½á¹¹Êý¾Ý£¿
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿ÊDz»ÊÇÓиöËùÓл¯ºÏÎïµÄ×ÏÍâͼÆ×¿âÖ®ÀàµÄ¶«Î÷£¿
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿ÇóÒ»¸ö»³ö»¯ºÏÎï½á¹¹Ê½À´¼ìË÷ÎÄÏ×µÄÍøÕ¾
ÒѾÓÐ20È˻ظ´
¡¾ÇóÖú¡¿ÇóÒ»¸ö»¯ºÏÎïµÄÈܽâÐÔ
ÒѾÓÐ21È˻ظ´

·çÐÐÕß007
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
- ÐÔ±ð: GG
- רҵ: ÓлúºÏ³É
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯ½á¹û£º¹²²éµ½13¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . drummondol ÏàËÆ¶È:60% Journal of Natural Products 1981 Vol 44 86-90 An Investigation of the Antitumor Activity of Sesbania drummondii Richard G. Powell, Cecil R. Smith Jr. Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . drummondol C13H20O4 ÏàËÆ¶È:60% Plant Diversity and Resources 2012 34 101-106 New Withanolides from Nicandra physaloides (Solanaceae) YI Qian-Kun, LI Bo, LIU Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 8a C33H42O9 ÏàËÆ¶È:53.3% Tetrahedron Letters 2004 45 6485-6488 Chemoselective synthesis of multiple epoxy-bridged tetrahydropyranone ring systems Sengodagounder Muthusamy, Janagiraman Krishnamurthi, Munirathnam Nethaji Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (1S,2S,6R) 2-methoxycarbonyl-1-hydroxy-6-methyl-bicyclo[4,4,0]-decan-7-one C13H20O4 ÏàËÆ¶È:53.3% Tetrahedron 2012 68 3457-3467 An easy route toward enantio-enriched polycyclic derivatives via an asymmetric domino conjugate reduction¨Caldol cyclization catalyzed by a chiral Cu(I) complex Julia Deschamp, Thomas Hermant, Olivier Riant Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (-)-phaseic acid ÏàËÆ¶È:53.3% Natural Products and Bioprospecting 2013 3 93-98 New spinosin derivatives from the seeds of Ziziphus mauritiana Bin Wang, Hong-Tao Zhu, Dong Wang, Chong-Ren Yang, Min Xu, Ying-Jun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ethyl (1R *,2R *,3S *,4R * )-2-benzamido-3,4-dihydroxycyclohexanecarboxylate C16H21NO5 ÏàËÆ¶È:53.3% Tetrahedron 2014 70 2515-2522 Stereocontrolled transformation of cyclohexene ¦Â-amino esters into syn- or anti-difunctionalized acyclic ¦Â2,3-amino acid derivatives Original Research Article Maria Cherepanova, Lor¨¢nd Kiss, Ferenc F¨¹löp Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Phaseic acid C15H20O5 ÏàËÆ¶È:53.3% Journal of Tropical and Subtropical Botany 2010 18 559-563 Flavans with Anti-HSV Activity from the Leaves of Ficus microcarpa L. HU, Yingjie, WU, Xiaoping, LIU, Ni, ZHANG, Fengxue, LU, Yuanyuan, ZHANG, Yuhu, FU, Linchun Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 2 C20H27NO9S ÏàËÆ¶È:52.9% Tetrahedron Letters 2000 41 7921-7923 Chemoenzymatic preparation of 4-O-acetyl sialic acid derivative Tzenge-Lien Shih, Mou-Chi Cheng, Shih-Hsiung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . N-[2(R),3 (R)-Diacetoxy-4-methoxybutanedioyl]-L-alaninebenzyl ester C19H23NO9 ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry 1996 4 901-916 Synthesis of five enantiomerically pure haptens designed for in vitro evolution of antibodies with peptidase activity J¨¹rgen Wagner, Richard A. Lerner, Carlos F. Barbas Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 2 C20H27NO9S ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 7921-7923 Chemoenzymatic preparation of 4-O-acetyl sialic acid derivative Tzenge-Lien Shih, Mou-Chi Cheng, Shih-Hsiung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N-Decanyl-1,6-dideoxynojirimycin C16H33NO3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 1605-1612 An expeditious one-pot synthesis of 1,6-dideoxy-N-alkylated nojirimycin derivatives and their inhibitory effects on the secretion of IFN-¦Ã and IL-4 Jian Zhou, Yongmin Zhang, Xia Zhou, Jing Zhou, Li-He Zhang, Xin-Shan Ye, Xiao-Lian Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 54 C18H24O5Se ÏàËÆ¶È:50% Tetrahedron 2013 69 7746-7758 Stereoselectivity of electrophile-promoted oxacyclizations of 1,4-dihydroxy-5-alkenes to 3-hydroxytetrahydropyrans Frank E. McDonald, Kento Ishida, Jessica A. Hurtak Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3-Keto-15-hydroxysclareolide C16H24O4 ÏàËÆ¶È:50% Journal of the Brazilian Chemical Society 2011 22 1177-1182 Biotransformation of Sclareolide by Filamentous Fungi: Cytotoxic Evaluations of the Derivatives Arturo Cano, Mar¨ªa Teresa Ram¨ªrez-Apan and Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-08-06 22:03:23














»Ø¸´´ËÂ¥
5