Synthetic approaches to gem-di-C-alkyl derivatives of carbohydrates: nucleophilic addition reactions of 3-C-methylene compounds derived from 1,2:5,6-di-O-isopropylidene-α-D-ribo-hexofuranos-3-ulose using phase-transfer catalysis
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference19 articles.
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Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Natural Product Synthesis Starting with Carbohydrates based on the Claisen Rearrangement Protocol;Stereoselective Synthesis;1992
2. Synthesis of Geminal Alkyl and Equatorially Functionalized Geminal Alkyl Derivatives of Hexopyranosides by Carbopalladation;Journal of Carbohydrate Chemistry;1989-07
3. Stereospecific access to equatorially functionalized geminal alkyl derivatives of hexopyranosides by cyclopalladation–oxidation;J. Chem. Soc., Chem. Commun.;1988
4. Synthesis of 2,2-Di-C-methyl-2-deoxy- and 4,4-Di-C-methyl-4-deoxypyranosides via Michael Addition of Conjugated Enopyranosiduloses;Bulletin of the Chemical Society of Japan;1987-04
5. TWO COMPLEMENTARY METHODS FOR INTRODUCTION OFgem-DIMETHYL GROUP IN HEXOPYRANOSIDE RING;Chemistry Letters;1985-07-05
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