期刊
ORGANIC LETTERS
卷 12, 期 15, 页码 3324-3327出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol100929z
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资金
- UC Davis Academic Senate Committee
- NIH/NIAID [R56AI80931-01]
- United States Department of Education
An efficient, convergent synthesis of totarol by a diastereoselective epoxide/alkene/arene bicyclization is described. The reported synthesis enables the preparation of related diterpenes totaradiol and totarolone as well as previously unavailable derivatives that exhibit comparable Inhibition of the bacterial cell division protein FtsZ.
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