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Structural Insights into the TES/TFA Reduction of Differently Substituted Benzofurans: Dihydrobenzofurans or Bibenzyls?
Synlett ( IF 2 ) Pub Date : 2020-10-22 , DOI: 10.1055/s-0040-1705949
Lucia Chiummiento 1 , Rosarita D’Orsi , Ilaria Caivano , Maria Funicello , Paolo Lupattelli
Affiliation  


Abstract

Various polysubstituted benzofurans were reduced by using triethylsilane in trifluoracetic acid. 2,3-Dihydrobenzofurans or bibenzyl compounds were obtained in high yields, depending on the nature of the substituents at C2 and on the benzene ring of the core structure. A p-anisole substituent at C2 of benzofurans always led to the corresponding bibenzyls.



Publication History

Received: 09 September 2020

Accepted after revision: 30 September 2020

Publication Date:
22 October 2020 (online)

© 2020. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany



中文翻译:

TES / TFA还原不同取代的苯并呋喃的结构见解:二氢苯并呋喃或联苄?


摘要

通过在三氟乙酸中使用三乙基硅烷还原各种多取代的苯并呋喃。取决于C2处取代基的性质以及核心结构的苯环,可以高收率获得2,3-二氢苯并呋喃或联苄化合物。甲p在苯并呋喃的C2 -苯甲醚取代基总是导致了相应的联苄类。



出版历史

收到:2020年9月9日

修订后接受:2020年9月30日

发布日期:
2020年10月22日(在线)

©2020年。Thieme。版权所有

Georg Thieme Verlag
KGRüdigerstraße14,70469斯图加特,德国

更新日期:2020-10-26
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