The development of N-aryl trifluoroacetimidate-based benzyl and allyl protecting group reagents-Reference-Cited by-同舟云学术

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The development of N-aryl trifluoroacetimidate-based benzyl and allyl protecting group reagents

Published:2013-12 Issue:51 Volume:54 Page:6983-6985
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tsabedze Sinele B.,Kabotso Daniel E.K.,Pohl Nicola L.B.

Funder

US National Science Foundation

the Joan and Marvin Carmack fund

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Protecting Groups in Carbohydrate Chemistry: Influence on Stereoselectivity of Glycosylations

2. Greene Protective Groups in Organic Synthesis;Greene,2006

3. Regio- and Stereocontrolled Selective Debenzylation and Substitution Reactions of C-2 Formyl Glycals. Application in the Synthesis of Constrained β-Sugar Amino Acids

4. Mix-and-Heat Benzylation of Alcohols Using a Bench-Stable Pyridinium Salt

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1. α-Selective glycosylations using glycosyl N-(ortho-methoxyphenyl)trifluoroacetimidates;Organic & Biomolecular Chemistry;2020

2. Comparison of disaccharide donors for heparan sulfate synthesis: uronic acids vs. their pyranose equivalents;Organic & Biomolecular Chemistry;2020

3. Trifluoroacetimidoyl halides: a potent synthetic origin;Organic Chemistry Frontiers;2020

4. Glycosyl nitrates in synthesis: streamlined access to glucopyranose building blocks differentiated at C-2;Organic & Biomolecular Chemistry;2018

5. A carbon tetrachloride-free synthesis of N -phenyltrifluoroacetimidoyl chloride;Carbohydrate Research;2017-10

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