Selective ring-opening reaction of styrene oxide with lithium azide in the presence of cyclodextrins in aqueous media-Reference-Cited by-同舟云学术

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Selective ring-opening reaction of styrene oxide with lithium azide in the presence of cyclodextrins in aqueous media

Published:1992-01 Issue:2 Volume:3 Page:247-250
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Guy Alain,Doussot Joël,Garreau Robert,Godefroy-Falguieres Annie

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference13 articles.

1. Enantioselective synthesis using chiral heterogeneous catalysts.

2. Selective aromatic substitution by hydrophobic binding of a substrate to a simple cyclodextrin catalyst

3. Selective syntheses using cyclodextrins as catalyst. 2. The para-oriented carboxylation of phenols

4. Cyclodextrin-H O: A New System for Asymmetric Epoxidation

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1. Ring-opening reactions in water;Green Sustainable Process for Chemical and Environmental Engineering and Science;2020

2. LiBr/β-CD/IBX/H2O-DMSO: A new approach for one-pot biomimetic regioselective ring opening of chalcone epoxides to bromohydrins and conversion to 1,2,3-triketones;Synthetic Communications;2017-05-05

3. Water as Reaction Medium in the Synthetic Processes Involving Epoxides;Green Solvents I;2012

4. Stereoselective Ring-Opening Reactions of Epoxides in Water;Current Organic Synthesis;2011-06-01

5. Ring‐Opening of Epoxides in Water;European Journal of Organic Chemistry;2011-03-30

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