Modular three-component solid-phase synthesis of unsymmetrical guanidines via resin capture of carbodiimides
Modular three-component solid-phase synthesis of unsymmetrical guanidines via resin capture of carbodiimides
Because of their basicity and hydrogen-bonding properties, guanidines are an important functional group in many biologically active compounds of natural or synthetic origin. Consequently, methodologies for the parallel synthesis of guanidines have attracted much attention from both academia and industry. Numerous solid-phase routes have been reported, and the vast majority of these involve either urea or thiourea precursors or guanidine synthesis from pseudoureas or similarly activated amidines.
substituted guanidines, n, n', n'-substituted guanidines, staudinger reaction, annulation reaction, cyclic guanidines, organic-synthesis, linker, strategy, derivatives, reagents
32-34
Boguszewski, Paul A.
a3204dc6-3471-456b-86d7-6fa08d043eb8
Rahman, Shahzad S.
1b62eb43-fac6-4fec-b8f8-b5c167b7b820
Ganesan, A.
62aa5a87-9308-4383-8686-99726b6bcfb9
2004
Boguszewski, Paul A.
a3204dc6-3471-456b-86d7-6fa08d043eb8
Rahman, Shahzad S.
1b62eb43-fac6-4fec-b8f8-b5c167b7b820
Ganesan, A.
62aa5a87-9308-4383-8686-99726b6bcfb9
Boguszewski, Paul A., Rahman, Shahzad S. and Ganesan, A.
(2004)
Modular three-component solid-phase synthesis of unsymmetrical guanidines via resin capture of carbodiimides.
Journal of Combinatorial Chemistry, 6 (1), .
(doi:10.1021/cc034036+).
Abstract
Because of their basicity and hydrogen-bonding properties, guanidines are an important functional group in many biologically active compounds of natural or synthetic origin. Consequently, methodologies for the parallel synthesis of guanidines have attracted much attention from both academia and industry. Numerous solid-phase routes have been reported, and the vast majority of these involve either urea or thiourea precursors or guanidine synthesis from pseudoureas or similarly activated amidines.
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Published date: 2004
Keywords:
substituted guanidines, n, n', n'-substituted guanidines, staudinger reaction, annulation reaction, cyclic guanidines, organic-synthesis, linker, strategy, derivatives, reagents
Identifiers
Local EPrints ID: 20139
URI: http://eprints.soton.ac.uk/id/eprint/20139
ISSN: 1520-4766
PURE UUID: ec646351-22e0-498e-9574-5a5421e28729
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Date deposited: 23 Feb 2006
Last modified: 15 Mar 2024 06:22
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Author:
Paul A. Boguszewski
Author:
Shahzad S. Rahman
Author:
A. Ganesan
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