COPPER-CATALYZED CONJUGATE ADDITIONS OF ORGANOZIRCONOCENES - SYNTHETIC AND MECHANISTIC STUDIES

被引：52

作者：

WIPF, P ^{[1
]}

XU, WJ ^{[1
]}

SMITROVICH, JH ^{[1
]}

LEHMANN, R ^{[1
]}

VENANZI, LM ^{[1
]}

机构：

[1] ETH ZENTRUM, INORGAN CHEM LAB, CH-8092 ZURICH, SWITZERLAND

来源：

TETRAHEDRON | 1994年 / 50卷 / 07期

关键词：

D O I：

10.1016/S0040-4020(01)85058-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

In the presence of 3-10 mol % of Cu(l) salts such as CuBr.SMe(2) or CuCN, alkylzirconocenes add readily to alpha,beta-unsaturated ketones, aldehydes, and sulfones. The reaction yield is sensitive to the presence of Lewis acids and bases. Steric hindrance as well as a broad range of functional groups are tolerated in the conjugate addition process. Unsaturated N-acyl oxazolidinones give high diastereoselectivities for the formation of the new asymmetric carbon. The resulting zirconium enolates can be used for tandem aldol addition reactions to aldehydes. Depending on the type of copper salt used, slow, or fast formation of copper mirror occurs, but no intermediate copper species is detected spectroscopically. Therefore, a mechanism involving enone complexation by the Lewis-acidic zirconocene followed by inner-sphere transfer of the alkyl substituent to chelated Cu(l) is proposed.

引用

页码：1935 / 1954

页数：20

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