Reactions of Imines, Nitriles, and Isocyanides with Pentaphenylborole: Coordination, Ring Expansion, C–H Bond Activation, and Hydrogen Migration Reactions-Reference-Cited by-同舟云学术

Reactions of Imines, Nitriles, and Isocyanides with Pentaphenylborole: Coordination, Ring Expansion, C–H Bond Activation, and Hydrogen Migration Reactions

Published:2015-09-01 Issue:18 Volume:54 Page:8957-8968
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Huang Kexuan¹,Couchman Shannon A.²,Wilson David J. D.²,Dutton Jason L.²,Martin Caleb D.¹

Affiliation:

1. Department of Chemistry and Biochemistry, Baylor University, One Bear Place #97348, Waco, Texas 76798, United States

2. Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria, Australia, 3086

Funder

Australian Research Council

Baylor University

Welch Foundation

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.5b01040

Reference76 articles.

1. Braunschweig, H.; Krummenacher, I.; Wahler, J.InAdvances in Organometallic Chemistry;Hill, A. F., Fink, M. J., Eds.Academic Press:San Diego, CA, 2013; Vol.61, p1.

2. Recent developments in the chemistry of antiaromatic boroles

3. Structural Evidence for Antiaromaticity in Free Boroles

4. Synthesis of pentaphenylborole, a potentially antiaromatic system

5. Derivative des borols

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