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Construction of Octahydro-4H-cyclopenta[b]pyridin-6-one Skeletons using Pot, Atom, and Step Economy (PASE) Synthesis.
Raju, Silver; Ghosh, Palash; Nayani, Kiranmai; Prashanth, Jupally; Sridhar, Balasubramanian; Mainkar, Prathama S; Chandrasekhar, Srivari.
Afiliação
  • Raju S; Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500007, India.
  • Ghosh P; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
  • Nayani K; Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500007, India.
  • Prashanth J; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
  • Sridhar B; Department of Organic Synthesis and Process Chemistry, CSIR-Indian Institute of Chemical Technology, Hyderabad, 500007, India.
  • Mainkar PS; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
  • Chandrasekhar S; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Chemistry ; 29(47): e202301058, 2023 Aug 21.
Article em En | MEDLINE | ID: mdl-37337465
ABSTRACT
Cascade aza-Piancatelli reaction and [3+3]/[4+2] cycloaddition reactions are carried out using the ideality principles of pot, atom, and step economy (PASE) synthesis. The reaction resulted in generation of octahydro-4H-cyclopenta[b]pyridin-6-one scaffolds. Moreover, octahydro-5,7a-epoxycyclopenta[cd]isoindol-4-one frameworks of gracilamine alkaloid and a novel decahydro-1H-dicyclopenta[cd,hi]isoindol-6-one were also realized in good yields with excellent regio- and diastereo-selectivities.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Health_economic_evaluation Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Health_economic_evaluation Idioma: En Ano de publicação: 2023 Tipo de documento: Article