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 |
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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