PALLADIUM - CATALYZED-REACTIONS OF TRIALKYLSTANNYL PHENYL SULFIDES WITH ALKENYL BROMIDES - A NEW DIASTEREOSELECTIVE SYNTHESIS OF (E)-1-ALKENYL PHENYL SULFIDES

被引：63

作者：

CARPITA, A ^{[1
]}

ROSSI, R ^{[1
]}

SCAMUZZI, B ^{[1
]}

机构：

[1] UNIV PISA,DIPARTIMENTO CHIM & CHIM IND,VIA RISORGIMENTO 35,I-56100 PISA,ITALY

来源：

TETRAHEDRON LETTERS | 1989年 / 30卷 / 20期

关键词：

D O I：

10.1016/S0040-4039(00)99102-0

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：2699 / 2702

页数：4

共 33 条

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[5] SYNTHESIS OF STEREOISOMERICALLY PURE (E)-1,5-DIYN-3-ENES AND (E)-1-BROMO-3-YN-1-ENES BY DIASTEREOSELECTIVE PALLADIUM-CATALYZED CROSS-COUPLING REACTION OF 1-ALKYNYLZINC CHLORIDES WITH A STEREOISOMERIC MIXTURE OF 1,2-DIBROMOETHYLENE
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[6] NEW SYNTHESIS OF ALPHA,BETA-UNSATURATED ALDEHYDES USING 1,3-BIS(METHYLTHIO)ALLYLLITHIUM
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[7] THE ROLE OF SULFUR FUNCTIONALITIES IN ACTIVATING AND DIRECTING OLEFINS IN CYCLO-ADDITION REACTIONS
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[9] STEREOSPECIFIC SYNTHESIS OF ALKENYL SULFIDES BY CROSS-COUPLING REACTIONS OF SECONDARY ALKYL GRIGNARD-REAGENTS WITH Z-1-BROMO-2-PHENYLTHIOETHENE OR E-1-BROMO-2-PHENYLTHIOETHENE IN THE PRESENCE OF TRANSITION-METAL CATALYSTS
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[10] A STEREOSPECIFIC ROUTE TO OLEFINS THROUGH SEQUENTIAL COUPLING REACTIONS OF GRIGNARD-REAGENTS WITH 1-BROMO-2-PHENYLTHIOETHENE IN THE PRESENCE OF NICKEL OR PALLADIUM CATALYSTS
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