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A theoretical study of the reaction of alkynylboranes with butadiene: competition between cycloaddition and alkynylboration.

作者信息

Silva María A, Pellegrinet Silvina C, Goodman Jonathan M

机构信息

Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom.

出版信息

J Org Chem. 2002 Nov 15;67(23):8203-9. doi: 10.1021/jo026324i.

DOI:10.1021/jo026324i
PMID:12423152
Abstract

The reactions of alkynyldihaloboranes and alkynyldialkylboranes with butadiene have been explored by using DFT methods at the B3LYP level with the 6-31G basis set. Transition structures for the concerted [4+2] cycloaddition have been found for the alkynylborane derivatives. Along with these, another reactive pathway has been found for the cycloaddition process with transition structures of high [4+3] character. The transition structures for the 1,4-alkynylboration processes have also been found. The geometries computed for the cycloaddition transition structure with high [4+3] character and the 1,4-alkynylboration transition structures are surprisingly similar though leading to different products. IRC calculations suggest that the [4+3] cycloaddition and alkynylboration pathways are associated by a zwitterionic structure.

摘要

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引用本文的文献

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RSC Adv. 2018 Oct 2;8(59):33864-33871. doi: 10.1039/c8ra07089j. eCollection 2018 Sep 28.