期刊
TETRAHEDRON
卷 66, 期 26, 页码 4730-4737出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2010.04.019
关键词
GPR40; Conjugate addition; Diastereoselective; Enantioselective; Oxazepanedione; Cinchonidine; beta-Alkynyl acid; Zincate
Two asymmetric methods to synthesize a potent GPR40 receptor agonist are reported. Both synthetic routes utilize readily available, inexpensive starting materials and reagents. The first route relies on a highly diastereoselective conjugate alkynylation of an ephedrine-derived oxazepanedione acceptor. The second route features the enantioselective alkynylation of a Meldrum's acid-derived acceptor mediated by a chiral zinc cinchonidine reagent. (C) 2010 Elsevier Ltd. All rights reserved.
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