ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Convenient Synthesis of Ferrocene Conjugates Mediated by Benzyltriethylammonium Tetrathiomolybdate in a Multi-Step Tandem Process

Sudhir, Sai V and Baig, Nasir Baig Rashid and Chandrasekaran, Srinivasan (2009) Convenient Synthesis of Ferrocene Conjugates Mediated by Benzyltriethylammonium Tetrathiomolybdate in a Multi-Step Tandem Process. In: European Journal of Organic Chemistry (31). pp. 5365-5372.

[img] PDF
5.pdf - Published Version
Restricted to Registered users only

Download (368Kb) | Request a copy
Official URL: http://www3.interscience.wiley.com/journal/1225991...

Abstract

The synthesis of a wide range of ferrocene-derived sulfur-linked mono- and disubstituted Michael adducts and conjugates mediated by benzyltriethylammonium tetrathiomolybdate (1) in a tandem process is reported. New route to access acryloylferrocene (4) and 1,1'-diacryloylferrocene (5) is discussed. Conjugation of amino acids to ferrocene is established via their N and C termini and also via side chains employing conjugate addition as key step to furnish mono-and divalent conjugates. This methodology has also been extended to access several ferrocene-carbohydrate conjugates. The electrochemical behavior of some selected ferrocene conjugates was studied by cyclic voltammetry.

Item Type: Journal Article
Additional Information: Copyright for this article belongs to Wiley.
Keywords: Sandwich complexes; Ferrocene conjugates; Cyclic voltammetry; Amino acids; Carbohydrates
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 01 Dec 2009 06:08
Last Modified: 01 Aug 2011 12:20
URI: http://eprints.iisc.ernet.in/id/eprint/25021

Actions (login required)

View Item View Item