Molecules 2013, 18(10), 12264-12289; doi:10.3390/molecules181012264

Schiff Bases: A Short Survey on an Evergreen Chemistry Tool

1email, 1email, 2,* email and 3,* email
Received: 10 August 2013; in revised form: 18 September 2013 / Accepted: 23 September 2013 / Published: 8 October 2013
(This article belongs to the Special Issue Named Organic Reactions based on Italian Chemists)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: The review reports a short biography of the Italian naturalized chemist Hugo Schiff and an outline on the synthesis and use of his most popular discovery: the imines, very well known and popular as Schiff Bases. Recent developments on their “metallo-imines” variants have been described. The applications of Schiff bases in organic synthesis as partner in Staudinger and hetero Diels-Alder reactions, as “privileged” ligands in the organometallic complexes and as biological active Schiff intermediates/targets have been reported as well.
Keywords: imines; Schiff bases; metallo-imines; salen complexes; bio-active-imines
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MDPI and ACS Style

Qin, W.; Long, S.; Panunzio, M.; Biondi, S. Schiff Bases: A Short Survey on an Evergreen Chemistry Tool. Molecules 2013, 18, 12264-12289.

AMA Style

Qin W, Long S, Panunzio M, Biondi S. Schiff Bases: A Short Survey on an Evergreen Chemistry Tool. Molecules. 2013; 18(10):12264-12289.

Chicago/Turabian Style

Qin, Wenling; Long, Sha; Panunzio, Mauro; Biondi, Stefano. 2013. "Schiff Bases: A Short Survey on an Evergreen Chemistry Tool." Molecules 18, no. 10: 12264-12289.

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