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Exploring the combinatorial explosion of amine-acid reaction space via graph editing.
Zhang, Rui; Mahjour, Babak; Outlaw, Andrew; McGrath, Andrew; Hopper, Tim; Kelley, Brian; Walters, W Patrick; Cernak, Tim.
Afiliação
  • Zhang R; Department of Chemistry, University of Michigan, Ann Arbor, MI, USA.
  • Mahjour B; Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI, USA.
  • Outlaw A; Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI, USA.
  • McGrath A; Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI, USA.
  • Hopper T; Relay Therapeutics, Cambridge, MA, USA.
  • Kelley B; Relay Therapeutics, Cambridge, MA, USA.
  • Walters WP; Relay Therapeutics, Cambridge, MA, USA.
  • Cernak T; Department of Chemistry, University of Michigan, Ann Arbor, MI, USA. tcernak@med.umich.edu.
Commun Chem ; 7(1): 22, 2024 Feb 03.
Article em En | MEDLINE | ID: mdl-38310120
ABSTRACT
Amines and carboxylic acids are abundant chemical feedstocks that are nearly exclusively united via the amide coupling reaction. The disproportionate use of the amide coupling leaves a large section of unexplored reaction space between amines and acids two of the most common chemical building blocks. Herein we conduct a thorough exploration of amine-acid reaction space via systematic enumeration of reactions involving a simple amine-carboxylic acid pair. This approach to chemical space exploration investigates the coarse and fine modulation of physicochemical properties and molecular shapes. With the invention of reaction methods becoming increasingly automated and bringing conceptual reactions into reality, our map provides an entirely new axis of chemical space exploration for rational property design.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article