6436-61-9Relevant articles and documents
A new and efficient multicomponent solid-phase synthesis of 2-acylaminomethylthiazoles
Henkel, Bernd,Sax, Michael,D?mling, Alexander
, p. 3679 - 3682 (2003)
A new multicomponent reaction (MCR) for the preparation of 2-substituted thiazole libraries using Rink amide resin is described. Thiazoles are assembled in a one-pot MCR of a thiocarboxylic acid, aldehyde, 3-(N,N-dimethylamino)-2-isocyanoacrylate with a resin-bound primary amine. Aliphatic and aromatic thiocarboxylic acids as well as aliphatic and (hetero-) aromatic aldehydes work in the reaction. Cleavage of the product yields the substituted thiazoles in reasonable to good purity.
Peptides. XXI. Dehydrogenation of some thiazolines derived from cysteine.
Barton,Kenner,Sheppard
, p. 1061 - 1065 (2007/10/05)
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