Palladium-catalysed nucleophilic release of allylic amines from a phenolic resin


Fisher, M. and Brown, R. C. D. (2001) Palladium-catalysed nucleophilic release of allylic amines from a phenolic resin. Tetrahedron Letters, 42, (46), 8227-8230. (doi:10.1016/S0040-4039(01)01739-7).

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Description/Abstract

2 circle Allylic alcohols were coupled to phenolic polystyrene resin under Mitsunobu conditions to provide substituted allyl ethers. which underwent efficient nucleophilic cleavage by 1 degrees and 2 degrees amines in the presence of catalytic palladium to afford allylic amines.

Item Type: Article
Related URLs:
Keywords: solid-phase synthesis, organic-synthesis, combinatorial chemistry, linkers
Subjects: Q Science
Q Science > QD Chemistry
Divisions: University Structure - Pre August 2011 > School of Chemistry
ePrint ID: 19477
Date Deposited: 14 Feb 2006
Last Modified: 27 Mar 2014 18:09
URI: http://eprints.soton.ac.uk/id/eprint/19477

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