Open AccessStereochemistry of Nucleophilic Addition Reactions. 5. Formation of Stabilized Ylides from Methyl 4,6-O-Benzylidene-2,3-dideoxy-3-nitro-β-D-erythro-hex-2-enopyranoside with SomeS-Ylides; An Important Role of the Nitro Group for Stabilization of the Ylides
Author(s) -
Tohru Sakakibara,
Rokuro Sudoh,
Toshio Nakagawa
Publication year - 1978
Publication title -
bulletin of the chemical society of japan
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.145
H-Index - 99
eISSN - 1348-0634
pISSN - 0009-2673
DOI - 10.1246/bcsj.51.1189
Subject(s) - chemistry , cyclopropane , nitro , diastereomer , ylide , nucleophile , stereochemistry , medicinal chemistry , nucleophilic addition , delocalized electron , ring (chemistry) , organic chemistry , alkyl , catalysis
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