A HIGHLY STEREOSELECTIVE TOTAL SYNTHESIS OF THE NATURAL ENANTIOMER OF OLIVIN

被引：40

作者：

ROUSH, WR ^{[1
]}

MICHAELIDES, MR ^{[1
]}

TAI, DF ^{[1
]}

CHONG, WKM ^{[1
]}

机构：

[1] MIT,DEPT CHEM,CAMBRIDGE,MA 02139

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1987年 / 109卷 / 24期

关键词：

D O I：

10.1021/ja00258a077

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：7575 / 7577

页数：3

共 24 条

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[6] THE REACTIONS OF COMBINED ORGANOCUPRATE CHLOROTRIMETHYLSILANE REAGENTS WITH CONJUGATED CARBONYL-COMPOUNDS
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[7] EVIDENCE FOR A REVERSIBLE D,PI-STAR-COMPLEXATION, BETA-CUPRATION SEQUENCE IN THE CONJUGATE ADDITION-REACTION OF GILMAN REAGENTS WITH ALPHA-ENONES, BETA-ENONES
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[9] STEREOSELECTIVE TOTAL SYNTHESIS OF THE NATURAL ENANTIOMER OF OLIVIN TRIMETHYL ETHER
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[10] SELECTIVE SYNTHESES WITH ORGANOMETALLICS .10. A CONVENIENT AND DIASTEREOSELECTIVE ROUTE TO HOMOALLYL ALCOHOLS - ADDITION OF (Z)-ALKENYL-DIMETHOXYBORANE OR (E)-ALKENYL-DIMETHOXYBORANE TO ALDEHYDES
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[J]. HELVETICA CHIMICA ACTA, 1982, 65 (04) : 1258 - 1263

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