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Please use this identifier to cite or link to this item: http://repositorio.ufba.br/ri/handle/ri/15860

Title: Aqueous Barbier allylation of aldehydes mediated by tin
Other Titles: Molecules
Authors: Guimarães, Ricardo L.
Lima, Dimas J. P.
Barros, Maria Ester de Sá Barreto
Cavalcanti, Lívia Nunes
Hallwass, Fernando
Navarro, Marcelo
Bieber, Lothar Wilhelm
Malvestiti, Ivani
Keywords: Fast Barbier reaction;Hydroxy and methoxy benzaldehydes;Aqueous;Tin
Issue Date: 2007
Abstract: The aqueous tin-mediated Barbier reaction affords good to excellent yields and moderate syn diastereoselectivity under basic and acidic conditions. The high yields and stereoselectivity observed in the case of o-substituted aldehydes suggest a cyclic organotin intermediate or transition state in K2HPO4 solution. A practical and efficient aqueous tin allylation of methoxy- and hydroxybenzaldehydes can be carried out in HCl solution in 15 minutes to afford the corresponding homoallylic alcohols in high yields. Aliphatic aldehydes give moderate to excellent yields with reaction times ranging from 30 to 60 minutes. Under these conditions, crotylation gives exclusively the γ-product and the syn isomer is formed preferentially. For 2-methoxybenzaldehyde, an equilibration of the isomers to a syn/anti ratio of 1:1 can be observed after several hours. Control experiments with radical sources or scavengers give no support for radical intermediates. NMR studies suggest a mechanism involving an organotin intermediate. The major organotin species formed depends on the reaction medium and the reaction time. The use of acidic solution reduces the reaction times, due to the acceleration of the formation of the allyltin(IV) species.
Description: Texto completo: acesso restrito. p. 2089-2105
URI: http://repositorio.ufba.br/ri/handle/ri/15860
ISSN: 1420-3049
Appears in Collections:Artigos Publicados em Periódicos (ICADS)

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