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Regio- and stereoselective base-catalyzed assembly of 6-methylene-5-oxaspiro[2.4]heptanones from alkynyl cyclopropyl ketones.
Samultceva, Sofia O; Dvorko, Marina Yu; Shabalin, Dmitrii A; Ushakov, Igor' A; Vashchenko, Alexander V; Schmidt, Elena Yu; Trofimov, Boris A.
Afiliação
  • Samultceva SO; A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, 1 Favorsky St, Irkutsk, 664033, Russian Federation. shabalin.chemistry@gmail.com.
  • Dvorko MY; A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, 1 Favorsky St, Irkutsk, 664033, Russian Federation. shabalin.chemistry@gmail.com.
  • Shabalin DA; A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, 1 Favorsky St, Irkutsk, 664033, Russian Federation. shabalin.chemistry@gmail.com.
  • Ushakov IA; A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, 1 Favorsky St, Irkutsk, 664033, Russian Federation. shabalin.chemistry@gmail.com.
  • Vashchenko AV; A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, 1 Favorsky St, Irkutsk, 664033, Russian Federation. shabalin.chemistry@gmail.com.
  • Schmidt EY; A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, 1 Favorsky St, Irkutsk, 664033, Russian Federation. shabalin.chemistry@gmail.com.
  • Trofimov BA; A.E. Favorsky Irkutsk Institute of Chemistry SB RAS, 1 Favorsky St, Irkutsk, 664033, Russian Federation. shabalin.chemistry@gmail.com.
Org Biomol Chem ; 20(26): 5325-5333, 2022 07 06.
Article em En | MEDLINE | ID: mdl-35735091
6-Methylene-5-oxaspiro[2.4]heptanones have been synthesized via base-catalyzed dimerization of available alkynyl cyclopropyl ketones. The reaction proceeds effectively in the presence of the t-BuOK/t-BuOH/THF catalytic system at room temperature to afford the desired spirocycles in a regio- and stereoselective manner. A wider synthetic utility of alkynyl cyclopropyl ketones as novel building blocks was demonstrated by the synthesis of diverse spirocyclopropanes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cetonas Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2022 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cetonas Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2022 Tipo de documento: Article País de publicação: Reino Unido