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Synthesis of alkynamides through reaction of alkyl- or aryl-substituted alkynylaluminums with isocyanates.
Cho, Soohong; Lee, Yeonjoo; Lee, Kyeongmin; Lee, Hwiwoong; Lee, Yunmi; Jung, Byunghyuck.
Afiliación
  • Cho S; Department of Chemistry, Kwangwoon University, Seoul 01897, Republic of Korea. ymlee@kw.ac.kr.
  • Lee Y; Department of Emerging Materials Science, DGIST, Daegu 42988, Republic of Korea. byunghyuck.jung@dgist.ac.kr.
  • Lee K; Department of Chemistry, Kwangwoon University, Seoul 01897, Republic of Korea. ymlee@kw.ac.kr.
  • Lee H; Department of Chemistry, Kwangwoon University, Seoul 01897, Republic of Korea. ymlee@kw.ac.kr.
  • Lee Y; Department of Chemistry, Kwangwoon University, Seoul 01897, Republic of Korea. ymlee@kw.ac.kr.
  • Jung B; Department of Emerging Materials Science, DGIST, Daegu 42988, Republic of Korea. byunghyuck.jung@dgist.ac.kr.
Org Biomol Chem ; 20(1): 139-151, 2021 12 22.
Article en En | MEDLINE | ID: mdl-34874041
ABSTRACT
An efficient and facile method for the preparation of alkynamides through Et3N-catalyzed alumination of alkyl- or aryl-substituted terminal alkynes with AlMe3 and sequential nucleophilic addition of in situ generated alkynylaluminums to isocyanates is described. This method has the merits of using readily available isocyanates and monosubstituted alkynes, easy access to organoaluminums, short reaction times, and high efficiency. A gram-scale synthesis of the desired alkynamide and its application to the formation of α-methylene-ß-lactams demonstrates the synthetic utility of this method.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2021 Tipo del documento: Article