A new route to keto and alkyl derivatives of (R)-carvone via diastereoselective conjugate addition of nitronate ions



Document title: A new route to keto and alkyl derivatives of (R)-carvone via diastereoselective conjugate addition of nitronate ions
Journal: Journal of the Brazilian Chemical Society
Database: PERIÓDICA
System number: 000311933
ISSN: 0103-5053
Authors: 1
2

Institutions: 1Centro Federal de Educacao Tecnologica de Quimica de Nilopolis, Nilopolis, Rio de Janeiro. Brasil
2Universidade Federal do Rio de Janeiro, Centro de Ciencias da Saude, Rio de Janeiro. Brasil
Year:
Season: Dic
Volumen: 17
Number: 7
Pages: 1229-1232
Country: Brasil
Language: Inglés
Document type: Artículo
Approach: Experimental, aplicado
English abstract The reactivity and diastereoselectivity of conjugate addition of different nitronates ions to (R)-carvone was systematically studied. The Michael adducts 2a-e were obtained in good yield and 3,2-cis-3,5-trans selectivity. The nitroadducts 2b,c were transformed via Nef reaction into (R)-carvone ketone derivatives 9,10 and nitroadducts 2b,d led to (R)-carvone alkylated derivatives 11,12, via a denitration reaction
Portuguese abstract A reatividade e diastereosseletividade da adição conjugada de íons nitronatos representativos à (R)-carvona foi estudada. Os adutos de Michael 2a-e foram obtidos em bom rendimento e boa 3,2-cis-3,5-trans-seletividade. Os nitroadutos 2b e 2c foram transformados via uma reação de Nef nos ceto-derivados 9 e 10 ao passo que uma reação de desnitração transformou 2b e 2d nos derivados alquilados da carvona 11 e 12
Disciplines: Química
Keyword: Química orgánica,
Síntesis orgánica,
Aniones nitroalquilo,
Adiciones de Michael,
Reacción de Nef,
Fluoruro de tetrabutilamonio
Keyword: Chemistry,
Organic chemistry,
Organic synthesis,
Nitroalkyl anions,
Michael additions,
Nef reaction,
Tetrabutylammonium fluoride
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