REGIOSELECTIVE ALLYLIC AMINATION CATALYZED BY IRON SALTS

被引：48

作者：

SRIVASTAVA, RS ^{[1
]}

NICHOLAS, KM ^{[1
]}

机构：

[1] UNIV OKLAHOMA,DEPT CHEM & BIOCHEM,NORMAN,OK 73019

来源：

TETRAHEDRON LETTERS | 1994年 / 35卷 / 47期

关键词：

D O I：

10.1016/S0040-4039(00)78485-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Alkenes react with phenylhydroxylamine in the presence of Fe(II) and Fe(III) salts to produce N-phenyl-N-allyl amines in moderate to good yields. Unsymmetrical substrates react with high regioselectivity giving the products of double bond transposition.

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页码：8739 / 8742

页数：4

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