Titanium promoted reduction of imines with Grignards, silanes, and zinc: identification of a new mechanism with silanes


Autoria(s): Kumar, Akshai; Pandiakumar, Arun Kumar; Samuelson, AG
Data(s)

2014

Resumo

Aldimines react with reducing agents, such as Grignards, phenylsilane or zinc in the presence of titanium(IV) isopropoxide to form amines and reductively coupled imines (diamines). Using deuterium labeled reagents, the mechanism of reduction to form amines is described. Reducing agents, such as the Grignard and zinc result in the formation of low valent titanium (LVT), which in turn reduces the imine. On the other hand, phenylsilane reacts by a distinctly different mechanism and where a hydrogen atom from silicon is directly transferred to the titanium coordinated imine. (c) 2014 Elsevier Ltd. All rights reserved.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/49161/1/tet_70-19_3185_2014.pdf

Kumar, Akshai and Pandiakumar, Arun Kumar and Samuelson, AG (2014) Titanium promoted reduction of imines with Grignards, silanes, and zinc: identification of a new mechanism with silanes. In: TETRAHEDRON, 70 (19). pp. 3185-3190.

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

http://dx.doi.org/10.1016/j.tet.2014.03.035

http://eprints.iisc.ernet.in/49161/

Palavras-Chave #Inorganic & Physical Chemistry
Tipo

Journal Article

PeerReviewed