期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 135, 期 30, 页码 10890-10893出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja405548b
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资金
- Amgen
- Bristol-Myers Squibb
- NSF [CHE-1058292]
- NIH [GM095076]
- Kitasato Institute
- Uehara Foundation
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1058292] Funding Source: National Science Foundation
This manuscript describes an enantioselective synthesis of the naturally occurring alkaloid citrinadin B. The synthetic effort revealed an anomaly in the original structural assignment that has led to the proposal of a stereochemical revision. This revision is consistent with the structures previously reported for a closely related family of alkaloids, PF1270A-C. The synthesis is convergent and employs a stereoselective intermolecular nitrone cyloaddition reaction as a key step.
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