relation: http://d-scholarship-dev.library.pitt.edu/17968/
title: The parent borylene: Betwixt and between
creator: Curran, DP
creator: Boussonnière, A
creator: Geib, SJ
creator: Lacôte, E
description: Still elusive: The reduction of dimethylimidazol-2-ylidene dichloroborane by sodium naphthalenide has been suggested to provide a borylene that cycloadds to naphthalene to make a borirane. Evidence has been provided that this borirane instead arises from coupling of a boryl radical and sodium naphthalenide. In contrast, reduction of 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene dichloroborane and the related dimesityl derivative provide novel C-H insertion products that may have arisen from a borylene. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
date: 2012-02-13
type: Article
type: PeerReviewed
format: text/plain
language: en
rights: attached
identifier: http://d-scholarship-dev.library.pitt.edu/17968/1/licence.txt
identifier:   Curran, DP and Boussonnière, A and Geib, SJ and Lacôte, E  (2012) The parent borylene: Betwixt and between.  Angewandte Chemie - International Edition, 51 (7).  1602 - 1605.  ISSN 1433-7851     
relation: 10.1002/anie.201107238