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General and Scalable Synthesis of 2-Aryl and 2-Alkyl Pyrimidines via an Electronically Tuned SNAr Approach.
Navuluri, Chandrasekhar; Su, Hsin Y; Sullivan, Ryan J; Lee, Taegyo; Jones, Brian P; Gorin, Boris; McWilliams, J Christopher; Nelson, Jade D; Alberico, Dino; Desrosiers, Jean-Nicolas.
Afiliación
  • Navuluri C; Eurofins CDMO Alphora Inc., 2070 Hadwen Road, Mississauga, Ontario L5K 2C9, Canada.
  • Su HY; Eurofins CDMO Alphora Inc., 2070 Hadwen Road, Mississauga, Ontario L5K 2C9, Canada.
  • Sullivan RJ; Eurofins CDMO Alphora Inc., 2070 Hadwen Road, Mississauga, Ontario L5K 2C9, Canada.
  • Lee T; Chemical Research & Development, Pfizer Worldwide Research & Development, Groton, Connecticut 06340, United States.
  • Jones BP; Chemical Research & Development, Pfizer Worldwide Research & Development, Groton, Connecticut 06340, United States.
  • Gorin B; Eurofins CDMO Alphora Inc., 2070 Hadwen Road, Mississauga, Ontario L5K 2C9, Canada.
  • McWilliams JC; Chemical Research & Development, Pfizer Worldwide Research & Development, Groton, Connecticut 06340, United States.
  • Nelson JD; Chemical Research & Development, Pfizer Worldwide Research & Development, Groton, Connecticut 06340, United States.
  • Alberico D; Eurofins CDMO Alphora Inc., 2070 Hadwen Road, Mississauga, Ontario L5K 2C9, Canada.
  • Desrosiers JN; Chemical Research & Development, Pfizer Worldwide Research & Development, Groton, Connecticut 06340, United States.
Org Lett ; 26(22): 4626-4630, 2024 Jun 07.
Article en En | MEDLINE | ID: mdl-38787438
ABSTRACT
An efficient SNAr approach for generating a wide array of 2-aryl and 2-alkyl pyrimidines in good to high yields was developed. This methodology does not require precious metal catalysts and is compatible with aryl, heteroaryl, and alkyl magnesium halides as nucleophiles. This process is scalable and performed at room temperature well below the temperature of the competing decomposition of the activated 2-tert-butyl sulfonyl pyrimidine electrophile.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Canadá
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