Studies on epoxidation of enantiomerically pure 2,3-dideoxy hex-2-enitols: a convenient access to highly functionalized enantiomerically pure tetrahydrofuran derivatives-Reference-Cited by-同舟云学术

Studies on epoxidation of enantiomerically pure 2,3-dideoxy hex-2-enitols: a convenient access to highly functionalized enantiomerically pure tetrahydrofuran derivatives

Published:2006-04 Issue:8 Volume:17 Page:1189-1198
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Sagar Ram,Reddy L. Vijaya Raghava,Shaw Arun K.

Publisher

Elsevier BV

Subject

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

Reference68 articles.

1. Formation of a hexoseptanose by unusual rearrangements of a furanoid glycal

2. Chemistry of sulfonylmethyl isocyanides. 30. A new synthesis of indoles by electrocyclic ring closure of dialkenylpyrroles. Synthesis of alkenylpyrroles from 1-tosylalkenyl isocyanides and Michael acceptors

3. Preparation of pyranoid glycal derivatives from phenyl thioglycosides and glycosyl phenyl sulphones

4. Synthesis of all 2,3,4-trimethoxy-5-hexenal (5,6-dideoxy-2,3,4-tri-O-methylaldohex-5-enose) isomers

5. Synthesis of Acyclic Unsaturated Sugar Derivatives

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