Control of stereoselectivity in samarium metal induced cyclopropanations. Synthesis of 1,25-dihydroxycholecalciferol-Reference-Cited by-同舟云学术

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Control of stereoselectivity in samarium metal induced cyclopropanations. Synthesis of 1,25-dihydroxycholecalciferol

Published:1991-05 Issue:21 Volume:32 Page:2343-2346
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kabat M.,Kiegiel J.,Cohen N.,Toth K.,Wovkulich P.M.,Uskoković M.R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. Cyclovitamins D3: the preparation of C6-ketocyclovitamin and its conversion to a ring B/C spirosteroid

2. Proc. Workshop Vitam. D;Wilson;7th Vitam. D: Mol.; Cell. Clin. Encocrinol.,1988

3. Lanthanides in organic synthesis. 7. Samarium-promoted, stereocontrolled cyclopropanation reactions

4. Samarium-promoted cyclopropanation of allylic alcohols

5. Homochiral ketals in organic synthesis. Diastereoselective cyclopropanation of α,β-unsaturated ketals derived from 1,4-D1-O-benzyl-l-threitol

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