期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 72, 期 20, 页码 7560-7566出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo070805q
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[GRAPHICS] A new route to alpha-keto acids is described, based on the ozonolysis of enol acetates obtained from alpha-substituted beta-keto esters. Escherichia coli branched chain aminotransferase (BCAT) activity toward a variety of substituted 2-oxoglutaric acids was demonstrated analytically. BCAT was shown to have a broad substrate spectrum, complementary to that of aspartate aminotransferase, and to offer access to a variety of glutamic acid analogues. The usefulness of BCAT was demonstrated through the synthesis of several 3- and 4-substituted derivatives.
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