Unexpected ring size effect of the annulation reaction of heterocyclic secondary enamines with dicarboxylic acid dichlorides

Ying Cheng; Hai Bo Yang; Mei Xiang Wang; David J. Williams

doi:10.1016/S0040-4020(02)00177-1

Unexpected ring size effect of the annulation reaction of heterocyclic secondary enamines with dicarboxylic acid dichlorides

Ying Cheng^*
, Hai Bo Yang
, Mei Xiang Wang
, David J. Williams

^*此作品的通讯作者

科研成果: 期刊稿件 › 文章 › 同行评审

14 引用（Scopus）

摘要

Heterocyclic enamines are versatile ambident nucleophilic reagents able to react with both aliphatic and aromatic dicarboxylic acid dichlorides in diverse manners. The reaction outcome was strongly dependent upon the heterocyclic structure of the enamines and the nature of the diacid dichlorides employed.

源语言	英语
页（从-至）	2821-2829
页数	9
期刊	Tetrahedron
卷	58
期	14
DOI	https://doi.org/10.1016/S0040-4020(02)00177-1
出版状态	已出版 - 1 4月 2002
已对外发布	是

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title = "Unexpected ring size effect of the annulation reaction of heterocyclic secondary enamines with dicarboxylic acid dichlorides",

abstract = "Heterocyclic enamines are versatile ambident nucleophilic reagents able to react with both aliphatic and aromatic dicarboxylic acid dichlorides in diverse manners. The reaction outcome was strongly dependent upon the heterocyclic structure of the enamines and the nature of the diacid dichlorides employed.",

keywords = "Annulation, Dicarboxylic acid dichlorides, Heterocyclic secondary enamines",

author = "Ying Cheng and Yang, \{Hai Bo\} and Wang, \{Mei Xiang\} and Williams, \{David J.\}",

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AU - Cheng, Ying

AU - Yang, Hai Bo

AU - Wang, Mei Xiang

AU - Williams, David J.

PY - 2002/4/1

Y1 - 2002/4/1

N2 - Heterocyclic enamines are versatile ambident nucleophilic reagents able to react with both aliphatic and aromatic dicarboxylic acid dichlorides in diverse manners. The reaction outcome was strongly dependent upon the heterocyclic structure of the enamines and the nature of the diacid dichlorides employed.

AB - Heterocyclic enamines are versatile ambident nucleophilic reagents able to react with both aliphatic and aromatic dicarboxylic acid dichlorides in diverse manners. The reaction outcome was strongly dependent upon the heterocyclic structure of the enamines and the nature of the diacid dichlorides employed.

KW - Annulation

KW - Dicarboxylic acid dichlorides

KW - Heterocyclic secondary enamines

UR - https://www.scopus.com/pages/publications/0036532581

U2 - 10.1016/S0040-4020(02)00177-1

DO - 10.1016/S0040-4020(02)00177-1

M3 - 文章

AN - SCOPUS:0036532581

SN - 0040-4020

VL - 58

SP - 2821

EP - 2829

JO - Tetrahedron

JF - Tetrahedron

IS - 14

ER -

Unexpected ring size effect of the annulation reaction of heterocyclic secondary enamines with dicarboxylic acid dichlorides

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