Stereoselective amino-hydroxylation of the double bond in 7-oxabicyclo[2.2.1]hept-5-en-2-yl derivatives. Remote substituent participation in acid-catalyzed decompositions of aziridines and triazolines-Reference-Cited by-同舟云学术

Stereoselective amino-hydroxylation of the double bond in 7-oxabicyclo[2.2.1]hept-5-en-2-yl derivatives. Remote substituent participation in acid-catalyzed decompositions of aziridines and triazolines

Published:1988 Issue:30 Volume:29 Page:3695-3698
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Reymond Jean-Louis,Vogel Pierre

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. The Preparation of Optically Pure 7-Oxabicyclo [2.2.1]hept-2-ene Derivatives. The CD Spectrum of (+)-(1R)-7-Oxabicyclo [2.2.1]hept-5-en-2-one

2. Optical resolution of 7-oxabicyclo[2.2.1]hept-21-ene derivatives. Diastereoselectivity in the formation of cyanohydrine-brucine complexes

3. Enzymatic preparation of optically active 7-oxabicyclo[2.2.1] heptane derivatives

4. Regioselectivity of electrophilic additions to 7-oxabicyclo[2.2.1]heptenes controlled by remote substituents. Arenesulfonyl substituted 7-oxabicyclo[2.2.1]heptenes as stereo- and regioselective chiral dienophiles

5. C-nucleosides and related compounds. Synthesis of D,L-3,4- isopropylidene-2,5-anhydroallose: a novel periodate cleavage

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