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), pp. 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
Digital Object Identifier (DOI): doi:10.1016/S0040-4039(01)01739-7
ISSNs: 0040-4039 (print)
Keywords: solid-phase synthesis, organic-synthesis, combinatorial chemistry, linkers
Subjects: Q Science
Q Science > QD Chemistry
ePrint ID: 19477
Date :
Date Event
12 November 2001Published
Date Deposited: 14 Feb 2006
Last Modified: 16 Apr 2017 23:02
Further Information:Google Scholar
URI: http://eprints.soton.ac.uk/id/eprint/19477

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