STEREOSELECTIVE SYNTHESIS OF 2-SUBSTITUTED 1-METHOXY-1,3-DIENES BY 1,4-ELIMINATION WITH TRIBUTYLSTANNYLLITHIUM

被引：4

作者：

FUJIWARA, S ^{[1
]}

KATSUMURA, S ^{[1
]}

ISOE, S ^{[1
]}

机构：

[1] OSAKA CITY UNIV,FAC SCI,INST ORGAN CHEM,SUGIMOTO 3-3-138,SUMIYOSHI KU,OSAKA 558,JAPAN

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 05期

关键词：

D O I：

10.1016/S0040-4039(00)94604-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Highly stereoselective synthesis of 2-substituted 1-methoxy-1,3-dienes was developed by 1,4-elimination of 2-substituted 4-chlorocrotonaldehyde dimethylacetal derivatives with tributylstannyllithium. © 1990.

引用

页码：691 / 694

页数：4

共 13 条

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[6] 1-ACETOXY AND 1-SILYLOXY-1,3-DIENES VIA REDUCTIVE HOMOLOGATION OF ALPHA,BETA-UNSATURATED ESTERS
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[7] ELIMINATION AND SUBSTITUTION IN THE REACTIONS OF VICINAL DIHALIDES AND OXYHALIDES WITH TRIMETHYLSTANNYLSODIUM - EFFECTS OF SOLVENT AND OF ION AGGREGATION ON COURSE AND STEREOCHEMISTRY
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[8] STEREOSPECIFIC SYNTHESIS OF Z-1-ALKOXY-1,3-BUTADIENES AND E-1-ALKOXY-1,3-BUTADIENES
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