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A new strategy for the stereoselective synthesis of 2,3-dideoxy-3-fluoro-D-ribofuranose derivatives
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作者 GUO, ZW huang, bg +2 位作者 XIAO, WJ HUI, YZ LANG, SA 《Chinese Journal of Chemistry》 SCIE CAS CSCD 1995年第4期363-367,共5页
The important intermediate for syntheses of various anti-HIV nucleoside analogues, methyl 2,3-dideoxy-3-fluoro-6-O-(p-methylbenzoyl)-alpha-D-ribofuranoside, was synthesized starting from 2-deoxy-D-ribose in 5 steps Wi... The important intermediate for syntheses of various anti-HIV nucleoside analogues, methyl 2,3-dideoxy-3-fluoro-6-O-(p-methylbenzoyl)-alpha-D-ribofuranoside, was synthesized starting from 2-deoxy-D-ribose in 5 steps With an overall yield of 24%. This strategy can be also used for synthesizing other analogues with various substitutions at 3-C position. 展开更多
关键词 NEW METHOD STEREOSELECTIVE SYNTHESIS 2 3-DIDEOXY-3-SUBSTITUTED-D-RIBOFURANOSIDE
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