期刊
ORGANIC LETTERS
卷 19, 期 7, 页码 1784-1787出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.7b00550
关键词
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资金
- Board of Research in Nuclear Sciences [2013/37C/51/BRNS]
- SERB, DST [EMR/2014/000235]
- University Grants Commission (UGC-ISF Project) [6-2/2016(IC)]
- CSIR New Delhi
Herein, we report, for the first time, a strategy to differerttiate O4/O4' positions of 1,1'-alpha,alpha-trehalose via, regioselective protection or site-selective functionalization and its application in. the first chemical synthesis, of succinoyl trehalose lipids. The biosurfactant glycolipids were obtained in 11-12 steps starting from trehalose in time span of 8=10 days and 11-12% overall yields.
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