期刊
TETRAHEDRON-ASYMMETRY
卷 19, 期 6, 页码 721-729出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2008.02.003
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A new stereodivergent synthesis towards piperidine iminosugar and azido lactones is described. The reaction of ethylidene-D-erythrose with amide sulfur ylides gave two isomeric trans-epoxyamides which were converted to 2-azido derivatives. Hydrolysis of the allo isomer gave 2-azido-1,4-lactone while the manno isomer gave the open chain epoxyamide. The latter gave a DMJ derivative in two steps. Direct hydrolysis of ethylidene epoxyamides gave the 3,6-anhydro glyconamides. (c) 2008 Elsevier Ltd. All rights reserved.
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