Regioselective reductions of 2,3-epoxy acetals with zinc-chlorotrimethylsilane and lithium aluminium hydride: convenient synthesis of 1,2 and 1,3-diones-Reference-Cited by-同舟云学术

Regioselective reductions of 2,3-epoxy acetals with zinc-chlorotrimethylsilane and lithium aluminium hydride: convenient synthesis of 1,2 and 1,3-diones

Published:1987-01 Issue:5 Volume:28 Page:551-554
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Vankar Yashwant D.,Chaudhuri Narayan C.,Rao C.Trinadha

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference6 articles.

1. 2Inc/Chlorotrimethns Ilane: A Mild Reducing System for the Conversion of Epoxides into Alcohols

2. Y.D. Vankar, G. Kumaravel, N. Mukherjee and C.T. Rao, Synthetic Communications (in the press) (For the reduction of conjugated ene-diones into 1,4-diketones).

3. Cycloalk-2-enones and α,β,α',β'-Cycloalkadienones. A. Synthesis. B. On the Direction of Bromination of 2-Substituted Cycloalkanones and Their Ketals

4. Bromohydrin formation in dimethyl sulfoxide

5. Base-catalyzed autoxidation of cyclic ketones

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