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gxyang

Òø³æ (СÓÐÃûÆø)

[ÇóÖú] ΢Æ×ÇóÖú

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11.69,13.97,14.49,14.98,16.19,,18.58,19.85,21.1,21.29,22.99,23.43,23.54,23.88,28.23,29.04,29.35,38.52,42.3,47.93,69.9,97.81,98.58,101.27,159,162.15,164.32,186.12,186.44
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Let'sdoit
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

yangyinhe

ÖÁ×ðľ³æ (ÖøÃûдÊÖ)

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gxyang: ½ð±Ò+10, ¡ïÓаïÖú, ̼Æ×¼Èë¶àÁ˶ººÅ£¬¿ÉÄÜÓ°ÏìÁ˼ìË÷½á¹û£¬ËùÒÔ¼ìË÷½á¹û¸ù±¾²»Æ¥Åä¡£¸úÌûÖÐÒѽ«¸ñʽÐÞÕý£¬Èç¹ûµÃµ½¸üºÃ½á¹û¿ÉÒÔ×·¼Ó½ð±Ò¡£ÎÞÂÛÈçºÎ»¹ÊÇҪллÏàÖú£¡ 2015-06-05 10:28:58
gxyang(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15 2015-06-30 17:18:56
1 .     ¦Ã-Lupane
    ÏàËÆ¶È:56.6%
Chinese Journal of Chemistry          1989          7          544-548
Studies on the synthesis of biomarkers: V. Synthesis of -lupane and its epimer
Tong-Shuang Li, Yu-Lin Li and Xiao-Tian Liang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     6-hydroxycholestan-3-thiosemicarbazone
C28H49N3OS     ÏàËÆ¶È:55.1%
Steroids          2014          87          99-107
Synthesis and antiproliferative activity of some steroidal thiosemicarbazones, semicarbazones and hydrozones
Chunfang Gan, Jianguo Cui, Shaoyang Su, Qifu Lin, Linyi Jia, Lianghua Fan, Yanmin Huang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     5¦Á,6¦Â-Dibromocholestan-3¦Â-ol
    ÏàËÆ¶È:53.5%
Steroids          2005          70          867-872
Electrochemical bromination of cholest-5-enes
Smiljka S. Milisavljević, Klaus Wurst, Gerhard Laus, Mirjana D. Vukićević, Rastko D. Vukićević
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     4¦Â-Chloro-5¦Á-cholestane-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:53.5%
Steroids          2007          72          95-104
4,5-Epoxycholestane-3,6-diols: Templates for generating the full set of eight cholestane-3,5,6-triol stereoisomers in multigram scales, but not for a cholestane-3,4,6-triol
Kejun Zhao, Yongfeng Wang, Li Han
Structure      13C NMR    Structure & 13C NMR    ̼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     3¦Â,6¦Â-dihydroxy-5¦Á-cholestane disulfate
    ÏàËÆ¶È:53.5%
Steroids          2009          74          1057-1060
Synthesis and cytotoxic analysis of some disodium 3¦Â,6¦Â-dihydroxysterol disulfates
Jianguo Cui, Hui Wang, Yanmin Huang, Yi Xin, Aimin Zhou
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     (1''S,3''S,5''R)-2-[[3''-[N-(2''''-methylpropyl)-2'''-acetamido]-6-methyl-(2''Z)-[(trimethylsilyl)methylene]cyclohexyl]ethyl]-2,5,5-trimethyl-1,3-dioxane
    ÏàËÆ¶È:53.5%
Journal of Medicinal Chemistry          1995          38          5038-5044
Structure-Activity Relationships of the Antimalarial Agent Artemisinin. 2. Effect of Heteroatom Substitution at O-11: Synthesis and Bioassay of N-Alkyl-11-aza-9-desmethylartemisinins
Mitchell A. Avery, Jason D. Bonk, Wesley K. M. Chong, Sanjiv Mehrotra, Robert Miller, Wilbur Milhous, D. Keith Goins, Sridhar Venkatesan, Christy Wyandt,
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     compound 6g
    ÏàËÆ¶È:53.5%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     compound 6i
    ÏàËÆ¶È:53.5%
Australian Journal of Chemistry          1981          34          1451-1465
Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols
JM Coxon and JR Gibson
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-06-04 13:42:49
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû

gxyang

Òø³æ (СÓÐÃûÆø)

ÒýÓûØÌû:
2Â¥: Originally posted by yangyinhe at 2015-06-04 13:42:49
1 .     ¦Ã-Lupane
    ÏàËÆ¶È:56.6%
Chinese Journal of Chemistry          1989          7          544-548
Studies on the synthesis of biomarkers: V. Synthesis of -lupane and its epimer
Tong-S ...

Ìṩ µÄÊý¾Ý¶àÁËÒ»¸ö¶ººÅ,¿ÉÄÜÓ°ÏìÁËÁ˼ìË÷½á¹û£ºÄÜ·ñÔÙÊÔÊÔ¿´£¬Ð»Ð»£¡
ë®´úÊÔ¼Á£¬d6-acetone
11.69,13.97,14.49,14.98,16.19,18.58,19.85,21.1,21.29,22.99,23.43,23.54,23.88,28.23,29.04,29.35,38.52,42.3,47.93,69.9,97.81,98.58,101.27,158.9,162.15,164.32,186.12,186.44
Let'sdoit
3Â¥2015-06-04 13:50:27
ÒÑÔÄ   »Ø¸´´ËÂ¥   ¹Ø×¢TA ¸øTA·¢ÏûÏ¢ ËÍTAºì»¨ TAµÄ»ØÌû
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