Chemical investigations in the synthesis of O-serinyl aminoribosides
Chemical investigations in the synthesis of O-serinyl aminoribosides
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DOI：
10.1016/j.tetasy.2005.11.019
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发表时间：
2006-01-09
影响因子：
--
通讯作者：
Le Merrer, Y
中科院分区：
文献类型：
--
作者：
Ginisty, M;Gravier-Pelletier, C;Le Merrer, Y
Glycosylation involving D-ribose derivatives and various N-protected tert-butyl L-serinates can be achieved efficiently by careful choice of the activation method at the anomeric position and of the Lewis acid promoter. The conditions described allow the major formation of the P-anomer required for further elaboration to liposidomycin and caprazamycin analogues. (c) 2005 Elsevier Ltd. All rights reserved.
