Conformational preferences of methacrolein in Diels-Alder and 1,3-dipolar cycloaddition reactions.

Barba, Carmen; Carmona, Daniel; García, José Ignacio; Lamata, María Pilar; Mayoral, José Antonio; Salvatella, Luis; Viguri, Fernando

Barba, Carmen; Carmona, Daniel; García, José Ignacio; Lamata, María Pilar; Mayoral, José Antonio; Salvatella, Luis; Viguri, Fernando.

Affiliation

Barba C; Departamento de Química InorgAnica, Instituto de Ciencia de Materiales de Aragón, Instituto Universitario de CatAlisis Homogénea, Facultad de Ciencias, Universidad de Zaragoza-CSIC, Pedro Cerbuna 12, E-50009 Zaragoza, Spain.

J Org Chem ; 71(26): 9831-40, 2006 Dec 22.

Article in En | MEDLINE | ID: mdl-17168603

Subject(s)

Acrolein/analogs & derivatives; Computer Simulation; Acrolein/chemical synthesis; Acrolein/chemistry; Aniline Compounds/chemistry; Benzylamines/chemistry; Boranes/chemistry; Cyclic N-Oxides/chemistry; Cyclization; Cyclopentanes/chemistry; Methylene Chloride/chemistry; Models, Molecular; Molecular Conformation; Nitrogen Oxides/chemistry; Pyrrolidines/chemistry; Stereoisomerism

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Collection: 01-internacional Database: MEDLINE Main subject: Acrolein / Computer Simulation Type of study: Prognostic_studies Language: En Journal: J Org Chem Year: 2006 Type: Article Affiliation country: Spain

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