Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/85149
Title: Azaborabutadienes: Synthesis by Metal-Free Carboboration of Nitriles and Utility as Building Blocks for B,N-Heterocycles
Authors: Kong, Lingbing
Lu, Wei
Li, Yongxin
Ganguly, Rakesh
Kinjo, Rei
Keywords: Carboboration
Azaborabutadiene
Issue Date: 2016
Source: Kong, L., Lu, W., Li, Y., Ganguly, R., & Kinjo, R. (2016). Azaborabutadienes: Synthesis by Metal-Free Carboboration of Nitriles and Utility as Building Blocks for B,N-Heterocycles. Angewandte Chemie International Edition, 55(47), 14718-14722.
Series/Report no.: Angewandte Chemie International Edition
Abstract: Metal-free regioselective carboboration of arylnitriles with L2PhB: (1: L=oxazol-2-ylidene) catalyzed by Et3B afforded the unprecedented acyclic 2-aza-4-borabutadienes 2, thus demonstrating a new strategy to construct a B,C,N-mixed π-system involving B=C and C=N bonds. Thermal isomerization of 2 gave C-borylimines (3), and diverse reactivity of 2 a towards several substrates, such as H+, F+, O2, S, Se, and isonitriles, allowed construction of boron-containing heterocycles with various ring sizes, thus illustrating the utility of 2 as a synthetic building block.
URI: https://hdl.handle.net/10356/85149
http://hdl.handle.net/10220/43658
ISSN: 1433-7851
DOI: 10.1002/anie.201608994
Rights: © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the author created version of a work that has been peer reviewed and accepted for publication by Angewandte Chemie International Edition, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1002/anie.201608994].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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