文献类型：期刊文献

英文题名：Asymmetric syntheses of (-)-methyl shikimate and (-)-5a-carba-β-D-gulopyranose from D-arabinose via Mukaiyama-type intramolecular aldolization

作者：Liu, Shi-Ling[1];Shi, Xiao-Xin[1];Xu, Yu-Lan[1];Xu, Wei[1];Dong, Jing[1]

机构：[1]E China Univ Sci & Technol, Dept Pharmaceut Engn, Sch Pharm, Shanghai 200237, Peoples R China

年份：2009

卷号：20

期号：1

起止页码：78

外文期刊名：TETRAHEDRON-ASYMMETRY

收录：;WOS:【SCI-EXPANDED(收录号:WOS:000264650100004)，CCR-EXPANDED(收录号:WOS:000264650100004)】；

基金：We thank the Chinese National Science Foundation (No. A-20172015) and Shanghai Educational Development Foundation (The Dawn Program: No. 03SG27) for the financial support of this work.

语种：英文

摘要：New asymmetric syntheses of (-)-methyl shikimate 1 and (-)-5a-carba-beta-D-gulopyranose 11 from D-arabinose through a common route which employed Mukaiyama-type intramolecular aldolization as a key step were described. (C) 2009 Elsevier Ltd. All rights reserved.