Regioselective Formation of Di-O-Benzyl-Substituted Hexopyranosides via Stannylene Acetal Intermediates-Reference-Cited by-同舟云学术

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Regioselective Formation of Di-O-Benzyl-Substituted Hexopyranosides via Stannylene Acetal Intermediates

Published:1994-04-01 Issue:3 Volume:13 Page:475-490
ISSN:0732-8303
Container-title:Journal of Carbohydrate Chemistry
language:en
Short-container-title:J. of Carbohydrate Chem.

Author:

Qin Huiping,Grindley T. Bruce

Publisher

Informa UK Limited

Subject

Organic Chemistry,Biochemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883

Cited by 28 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. Easy access to a carbohydrate-based template for stimuli-responsive surfactants;Beilstein Journal of Organic Chemistry;2020-11-17

2. Enzyme-Catalyzed Regioselective Acetylation of Functionalized Glycosides;European Journal of Organic Chemistry;2020-06-23

3. Glycosidic linkage, N-acetyl side-chain, and other structural properties of methyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1→4)-β-D-mannopyranoside monohydrate and related compounds;Acta Crystallographica Section C Structural Chemistry;2020-02-20

4. Tin-Mediated Regioselective Benzylation and Allylation of Polyols: Applicability of a Catalytic Approach Under Solvent-Free Conditions;The Journal of Organic Chemistry;2013-12-10

5. A Tin-Free Regioselective Radical De-O-benzylation by an Intramolecular Hydrogen Atom Transfer on Carbohydrate Templates;Angewandte Chemie International Edition;2013-06-04

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