A rational approach to chiral α-hydroxy aryl ketones from chiral aryl epoxides via regioselective, stereo retentive oxidative epoxide opening: Its application to the synthesis of antifungal Sch 42427/SM 9164-Reference-Cited by-同舟云学术

A rational approach to chiral α-hydroxy aryl ketones from chiral aryl epoxides via regioselective, stereo retentive oxidative epoxide opening: Its application to the synthesis of antifungal Sch 42427/SM 9164

Published:1994-11 Issue:45 Volume:35 Page:8299-8302
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Gala Dinesh,DiBenedetto Donald J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

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2. Asymmetric hydroxylation of enolates with N-sulfonyloxaziridines

3. Selective oxidation of optically active sec,sec-1,2-diols by dioxiranes. A practical method for the synthesis of homochiral .alpha.-hydroxy ketones in high optical purity

4. Saji, T.; Ohashi, N.; Tamoto, K.; Tanio, T.; Okuda, T.; Atsumi, T., 28th ICAAC Conference, Los Angeles, U.S.A., 1988, Abstract No. 173

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