期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2011, 期 30, 页码 5959-5961出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201101038
关键词
Inhibitors; Asymmetric synthesis; Fluorine; Organocatalysis
资金
- Ministry of Education, Science, Sports and Culture, Japan [21390030, 22106515, 2105]
- Asahi Glass Foundation
- Grants-in-Aid for Scientific Research [10J08891, 22106515, 21390030] Funding Source: KAKEN
The organocatalyzed asymmetric synthesis of efavirenz was achieved in five steps from a commercially available substrate through the operationally simple, enantioselective trifluoromethylation of an alkynyl ketone by using the Ruppert-Prakash reagent. The present method provides the first example of the enantioselective synthesis of efavirenz by using a direct trifluoromethylation approach.
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