Aryl vinyl cyclopropane Cope rearrangements

被引:6
作者
Allegre, Kevin [1 ]
Tunge, Jon [1 ]
机构
[1] Univ Kansas, 1567 Irving Hill Rd, Lawrence, KS 66045 USA
基金
美国国家科学基金会;
关键词
Vinyl cyclopropane; 3,3] sigmatropic rearrangement; Cope rearrangement; Epimerization; Medium ring; 3+2 CYCLOADDITION; ALLYLIC ALKYLATION; CARBON ACIDS; CHEMISTRY; CLAISEN; VINYLCYCLOPROPANES; CONSTRUCTION; PALLADIUM(0); ACIDITIES; ESTERS;
D O I
10.1016/j.tet.2019.04.061
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
While the divinyl cyclopropane Cope rearrangement is well-known, and has been broadly applied in synthesis, examples of the aryl vinyl cyclopropane Cope rearrangement are less common and generally limited in scope or reaction yield. The aryl vinyl cyclopropane Cope rearrangement gives access to the benzocycloheptene scaffold, which is present in a variety of naturally occurring and medicinally relevant products. Herein we report a method to obtain either of two regioisomeric benzocycloheptene products via an aryl vinyl cyclopropane Cope rearrangement, featuring additive-controlled regioselectivity. Mechanistic studies indicate a dynamic equilibration of cyclopropane stereoisomers, followed by rear-rangement of the cis diastereomer. (C) 2019 Published by Elsevier Ltd.
引用
收藏
页码:3319 / 3329
页数:11
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