Recent Advances in the Direct Nucleophilic Substitution of Allylic Alcohols through SN1-Type Reactions


Autoria(s): Baeza, Alejandro; Nájera Domingo, Carmen
Contribuinte(s)

Universidad de Alicante. Departamento de Química Orgánica

Nuevos Materiales y Catalizadores (MATCAT)

Síntesis Asimétrica (SINTAS)

Data(s)

22/09/2016

22/09/2016

2014

Resumo

Direct nucleophilic substitution reactions of allylic alcohols are environmentally friendly, since they generate only water as a byproduct, allowing access to new allylic compounds. This reaction has, thus, attracted the interest of the chemical community and several strategies have been developed for its successful accomplishment. This review gathers the latest advances in this methodology involving SN1-type reactions.

Spanish Ministerio de Ciencia e Innovación (MICINN) (projects CTQ2010-20387 and Consolider Ingenio 2010, CSD2007-00006), FEDER, the Generalitat Valenciana (PROMETEO 2009/039) and the University of Alicante are gratefully acknowledged for financial support. A.B. would also like to thank MICINN for a Juan de la Cierva contract (JCI-2009-03710) and the University of Alicante (Project GRE12-03).

Identificador

Synthesis. 2014, 46(01): 25-34. doi:10.1055/s-0033-1340316

0039-7881 (Print)

1437-210X (Online)

http://hdl.handle.net/10045/58135

10.1055/s-0033-1340316

Idioma(s)

eng

Publicador

Georg Thieme Verlag

Relação

http://dx.doi.org/10.1055/s-0033-1340316

Direitos

© Georg Thieme Verlag Stuttgart · New York

info:eu-repo/semantics/restrictedAccess

Palavras-Chave #SN1 reaction #Allylic substitution #Carbocations #Allylic alcohols #Green chemistry #Química Orgánica
Tipo

info:eu-repo/semantics/article