A head-to-head comparison of α- and β-alkoxy effects on stereoselectivity. Nucleophilic additions to a cyclohexanone substituted with five axial CO bonds-Reference-Cited by-同舟云学术

A head-to-head comparison of α- and β-alkoxy effects on stereoselectivity. Nucleophilic additions to a cyclohexanone substituted with five axial CO bonds

Published:1999-08 Issue:33 Volume:40 Page:5971-5974
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Paquette Leo A.,Tae Jinsung

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

2. Torsional strain involving partial bonds. The steric course of the reaction between allyl magnesium bromide and 4-t-butyl-cyclohexanone

3. Preparation of cyclopentadienes and diazocyclopentadienesvia cyclopentenolones and cyclopentenones

4. Stereochemistry of organometallic compound addition to ketones

5. Theory and Modeling of Stereoselective Organic Reactions

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