| Literature DB >> 17096579 |
Jong Yeon Hwang1, Hyung-Sub Choi, Jin-soo Seo, Hyun-Ju La, Sung-eun Yoo, Young-Dae Gong.
Abstract
A 2000-member library of benzopyran analogues was prepared by using a solid-phase synthesis protocol. Polymer-bound 6-alkylaminobenzopyrans 7 were synthesized as part of a first generation diversification step by employing reactions of a variety of alkyl halides with the amine 6. Transformations of the resin-bound intermediates 8 formed in this manner by reactions with acid halides, sulfonyl chlorides, and isocyanates leads to introduction of the second level of diversification found in the series of 6-alkylamino-2-(functionalized-aminomethyl)-2-methyl-2H-1-benzopyran analogues 11 and 12.Entities:
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Year: 2006 PMID: 17096579 DOI: 10.1021/cc0600526
Source DB: PubMed Journal: J Comb Chem ISSN: 1520-4766