Comparing B–H Bond Activation in Ni<sup>II</sup>X(NNN)-Catalyzed Nitrile Dihydroboration (X = Anionic N-, C-, O-, S-, or P-donor)-Reference-Cited by-同舟云学术

Comparing B–H Bond Activation in Ni^IIX(NNN)-Catalyzed Nitrile Dihydroboration (X = Anionic N-, C-, O-, S-, or P-donor)

Published:2022-12-01 Issue:49 Volume:61 Page:19998-20007
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Ataie Saeed¹,Baker R. Tom¹^ORCID

Affiliation:

1. Department of Chemistry and Biomolecular Sciences and Centre for Catalysis Research and Innovation, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada

Funder

Canada Research Chairs

Natural Sciences and Engineering Research Council of Canada

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.2c03273

Reference57 articles.

1. Aminoboranes as “Compatible” Iminium Ion Generators in Aminative C−C Bond Formations

2. Aminoboration: Addition of B–N σ Bonds across C–C π Bonds

3. Readily Available Primary Aminoboranes as Powerful Reagents for Aldimine Synthesis

4. Double and Single Hydroboration of Nitriles Catalyzed by a Ruthenium–Bis(silyl)xanthene Complex: Application to One-Pot Synthesis of Diarylamines and N-Arylimines

5. Efficient Cobalt Catalyst for Ambient-Temperature Nitrile Dihydroboration, the Elucidation of a Chelate-Assisted Borylation Mechanism, and a New Synthetic Route to Amides

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