Diastereo- and regioselective petasis aryl and allyl boration of ninhydrins towards synthesis of functionalized indene-diones and dihydrobenzoindeno-oxazin-ones.

Sengupta, Ayon; Maity, Suvendu; Saha, Pinaki; Ghosh, Prasanta; Rudra, Sonali; Mukhopadhyay, Chhanda

Sengupta, Ayon; Maity, Suvendu; Saha, Pinaki; Ghosh, Prasanta; Rudra, Sonali; Mukhopadhyay, Chhanda.

Afiliação

Sengupta A; Department of Chemistry, University of Calcutta, 92 APC Road, Kolkata, 700009, India.
Maity S; TCG Lifesciences Pvt. Ltd., BN 7, Sector V, Salt Lake City, Kolkata, 700091, India.
Saha P; Department of Chemistry, R.K. Mission Residencial College, Narendrapur, Kolkata, 700103, India.
Ghosh P; Department of Chemistry, R.K. Mission Residencial College, Narendrapur, Kolkata, 700103, India.
Rudra S; Department of Chemistry, R.K. Mission Residencial College, Narendrapur, Kolkata, 700103, India.
Mukhopadhyay C; TCG Lifesciences Pvt. Ltd., BN 7, Sector V, Salt Lake City, Kolkata, 700091, India. sonali.rudra@tcgls.com.

Mol Divers ; 27(3): 1385-1400, 2023 Jun.

Article em En | MEDLINE | ID: mdl-35913662

Assuntos

Ácidos Borônicos; Ninidrina; Estereoisomerismo; Ácidos Borônicos/química; Fenóis/química

Palavras-chave

Catalyst free; Diastereo- and regioselective; Easily available starting materials; Functionalized indene-diones and dihydrobenzo-indenooxazinones; Ninhydrin as carbonyl source; Petasis Borono Mannich reaction

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácidos Borônicos / Ninidrina Idioma: En Revista: Mol Divers Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Índia

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