IMPROVED SYNTHETIC ROUTES TO PROSTAGLANDINS UTILIZING SULFIDE-MEDIATED OXIDATION OF PRIMARY AND SECONDARY ALCOHOLS

被引：103

作者：

COREY, EJ ^{[1
]}

KIM, CU ^{[1
]}

机构：

[1] HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1973年 / 38卷 / 06期

关键词：

D O I：

10.1021/jo00946a041

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：1233 / 1234

页数：2

共 10 条

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[4] TOTAL SYNTHESIS OF PROSTAGLANDINS F2ALPHA AND E2 AS NATURALLY OCCURRING FORMS [J].

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[6] REAGENTS FOR STEREOSELECTIVE CARBONYL REDUCTION - IMPROVED SYNTHETIC ROUTE TO PRIMARY PROSTAGLANDINS [J].

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[7] STEREO-CONTROLLED SYNTHESIS OF PROSTAGLANDINS F2ALPHA AND E2 (DL) [J].

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[8] NEW AND HIGHLY EFFECTIVE METHOD FOR OXIDATION OF PRIMARY AND SECONDARY ALCOHOLS TO CARBONYL-COMPOUNDS [J].

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[9] SULFOXIDE-CARBODIIMIDE REACTIONS .I. A FACILE OXIDATION OF ALCOHOLS [J].

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