Selectivity in the Elaboration of Bicyclic Borazarenes.

Bhattacharjee, Ayan; Davies, Geraint H M; Saeednia, Borna; Wisniewski, Steven R; Molander, Gary A

Bhattacharjee, Ayan; Davies, Geraint H M; Saeednia, Borna; Wisniewski, Steven R; Molander, Gary A.

Afiliação

Bhattacharjee A; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, United States.
Davies GHM; Small Molecule Drug Development, Bristol Myers Squibb Company, 200 Cambridge Park Drive, Cambridge, Massachusetts 02140, United States.
Saeednia B; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, United States.
Wisniewski SR; Chemical Process Development, Bristol Myers Squibb Company, One Squibb Drive, New Brunswick, New Jersey 08903, United States.
Molander GA; Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323, United States.

Adv Synth Catal ; 363(9): 2256-2273, 2021 Apr 27.

Article em En | MEDLINE | ID: mdl-34335130

ABSTRACT

ABSTRACT

Among aromatic compounds, borazarenes represent a significant class of isosteres in which carbon-carbon bonds have been replaced by B-N bonds. Described herein is a summary of the selective reactions that have been developed for known systems, as well as a summary of computationally-based predictions of selectivities that might be anticipated in reactions of yet unrealized substructures.

Palavras-chave

Bicyclics; Borazarenes; Computations; Isosteres; Selectivity

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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