Comparing of endocyclic and exocyclic cleavage reactions using mycothiol synthesis as an example-Reference-Cited by-同舟云学术

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Comparing of endocyclic and exocyclic cleavage reactions using mycothiol synthesis as an example

Published:2018-05 Issue:20 Volume:74 Page:2440-2446
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Manabe Shino,Ito Yukishige

Funder

Japan Society for Promotion of Science

Yamada Science Foundation

Takeda Science Foundation

A-STEP

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Opportunities and challenges in synthetic oligosaccharide and glycoconjugate research

2. The impact of oxacarbenium ion conformers on the stereochemical outcome of glycosylations

3. Stereocontrolled 1,2-cis glycosylation as the driving force of progress in synthetic carbohydrate chemistry

4. Evidence for Endocyclic Cleavage of Conformationally Restricted Glycopyranosides

5. Study of the Endocyclic versus Exocyclic C–O Bond Cleavage Pathways of α- and β-Methyl Furanosides

Cited by 1 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. Lewis acid promoted anomerisation of alkyl O- and S-xylo-, arabino- and fucopyranosides;Carbohydrate Research;2019-01

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