Abstract
A convergent asymmetric total synthesis of (+)-danicalipin A is accomplished, in which two chlorinated fragments are stereoselectively joined by 1,3-dipolar coupling, leading to the confirmation of the absolute configuration of the natural product.(Figure Presented)
| Original language | English |
|---|---|
| Pages (from-to) | 908-911 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 13 |
| Issue number | 5 |
| DOIs | |
| Publication status | Published - Mar 4 2011 |
| Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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Cite this
Yoshimitsu, T., Nakatani, R., Kobayashi, A., & Tanaka, T. (2011). Asymmetric total synthesis of (+)-danicalipin A. Organic Letters, 13(5), 908-911. https://doi.org/10.1021/ol1029518