期刊
ORGANIC LETTERS
卷 13, 期 1, 页码 66-69出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol102549a
关键词
-
资金
- National Institutes of Health
A stereoselective synthesis of (+)-herboxidiene is described. The convergent synthesis utilized a Suzuki cross-coupling reaction to assemble the key segments. The synthesis of the functionalized tetrahydropyran ring utilized an Achmatowicz reaction as the key step. The synthesis of the C10-C19 segment was accomplished using Brown's crotylboration, asymmetric alkylation, and a stereoselective allylic chlorination reactions.
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