Journal
ORGANIC LETTERS
Volume 13, Issue 5, Pages 908-911Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol1029518
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Funding
- Ministry of Education, Culture, Sports, Science and Technology of Japan [22136006]
- Grants-in-Aid for Scientific Research [21590009] Funding Source: KAKEN
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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.
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