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Substrate-Controlled Three-Component Synthesis of Diverse Fused Heterocycles.
Peshkov, Anatoly A; Gapanenok, Diana; Puzyk, Aleksandra; Amire, Niyaz; Novikov, Alexander S; Martynova, Sofia D; Kalinin, Stanislav; Dar'in, Dmitry; Peshkov, Vsevolod A; Krasavin, Mikhail.
Afiliação
  • Peshkov AA; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
  • Gapanenok D; Nazarbayev University, Department of Chemistry, School of Sciences and Humanities, Nur-Sultan 010000, Kazakhstan.
  • Puzyk A; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
  • Amire N; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
  • Novikov AS; Nazarbayev University, Department of Chemistry, School of Sciences and Humanities, Nur-Sultan 010000, Kazakhstan.
  • Martynova SD; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
  • Kalinin S; Research Institute of Chemistry, Peoples' Friendship University of Russia (RUDN University), Moscow 117198, Russian Federation.
  • Dar'in D; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
  • Peshkov VA; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
  • Krasavin M; Institute of Chemistry, Saint Petersburg State University, Saint Petersburg 199034, Russian Federation.
J Org Chem ; 88(15): 10508-10524, 2023 Aug 04.
Article em En | MEDLINE | ID: mdl-37459446
A chemoselective strategy toward a variety of fused heterocyclic scaffolds relying on a three-component condensation of heterocyclic ketene aminals (HKAs) or corresponding thioaminals with aryl glyoxals and cyclic 1,3-dicarbonyl compounds has been developed and explored. Depending on the applied combination of substrates, the strategy can be tuned to provide straightforward access to imidazo[1,2-a]quinoline, pyrrolo[1,2-a]imidazole, and pyrrolo[2,1-b]thiazole frameworks.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2023 Tipo de documento: Article País de publicação: Estados Unidos