STEREOSELECTIVE HYDROXYLATION OF A PEPTIDE SIDE-CHAIN - THE SYNTHESIS OF THE ECHINOCANDIN RIGHT-HALF EQUIVALENT

被引：7

作者：

SAKAITANI, M ^{[1
]}

OHFUNE, Y ^{[1
]}

机构：

[1] SUNTORY INST BIOORGAN RES,SHIMAMOTO CHO,MISHIMA,OSAKA 618,JAPAN

来源：

TETRAHEDRON LETTERS | 1989年 / 30卷 / 17期

关键词：

D O I：

10.1016/S0040-4039(00)99661-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：2251 / 2254

页数：4

共 12 条

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[8] TOTAL SYNTHESIS OF ECHINOCANDINS .2. TOTAL SYNTHESIS OF ECHINOCANDIN-D VIA EFFICIENT PEPTIDE COUPLING REACTIONS [J].

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[9] AN EFFICIENT ROUTE TO 1,3-AMINO HYDROXYL SYSTEM VIA ELECTROPHILIC LACTONIZATION OF 2-AMINO-4-PENTENOIC ACID-DERIVATIVES - STEREOSELECTIVE SYNTHESIS OF (-)-BULGECININE [J].

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[10] A NEW MODE OF CYCLIC CARBAMATE FORMATION VIA TERT-BUTYLDIMETHYLSILYL CARBAMATE - STEREOSELECTIVE SYNTHESIS OF STATINE AND ITS ANALOG [J].

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