| Literature DB >> 19954974 |
Francesco Piscitelli1, Carlo Ballatore, Amos B Smith.
Abstract
A traceless solid supported protocol for the synthesis of 2-aminobenzothiazoles is described, employing resin-bound acyl-isothiocyanate and a series of anilines. Cyclization of the resulting N-acyl, N'-phenyl-thioureas generates the 2-aminobenzothiazole scaffold, which can be further elaborated prior to hydrazine-mediated cleavage of the final products from the carboxy-polystyrene resin. A small, focused library of 2-aminobenzothiazoles was prepared. Copyright 2009 Elsevier Ltd. All rights reserved.Entities:
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Year: 2009 PMID: 19954974 PMCID: PMC2818510 DOI: 10.1016/j.bmcl.2009.11.055
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823