Azabrendanes. III. Synthesis of stereoisomeric exo- and endo-5-acylaminomethyl-exo-2,3-epoxybicyclo[2.2.1]heptanes and their reduction by lithium aluminum hydride-Reference-Cited by-同舟云学术

Azabrendanes. III. Synthesis of stereoisomeric exo- and endo-5-acylaminomethyl-exo-2,3-epoxybicyclo[2.2.1]heptanes and their reduction by lithium aluminum hydride

Published:2001 Issue:3 Volume:12 Page:119-130
ISSN:1042-7163
Container-title:Heteroatom Chemistry
language:en
Short-container-title:Heteroatom Chem.

Author:

Kasyan Lilija I.,Tarabara Igor N.,Savel'yeva Oxana A.,Kasyan Andrey O.

Publisher

Wiley

Subject

General Chemistry

Reference39 articles.

1. New synthesis of 2-exo-brendanol

2. Intramolecular trapping by epoxides of intermediates generatedby organocuprate additions to propiolate esters.

3. Heterocage Compound [1]. Synthesis of Oxacage Tricyclic Systems: Oxabrendane, Oxahomobrendane, Oxaisotwistane, Oxahomoisotwistane and Oxatwistbrendane Skeleton with an Amino Function

4. Enzymatic preparation of optically active bicyclo[2.2.1]heptene derivatives, building blocks for terpenoid natural products. An attractive alternative to enantioselective Diels–Alder syntheses

5. 40. Aspects of stereochemistry. Part XI. Epoxide formation in the cyclohexene and bicycloheptene series

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