Journal
ORGANIC LETTERS
Volume 11, Issue 1, Pages 113-116Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol8024555
Keywords
-
Categories
Funding
- NOVARTIS Foundation (Japan)
- Ministry of Education, Culture, Sports, Science and Technology of Japan
Ask authors/readers for more resources
Stereoselective synthesis of a trans-fused 7,6,6,7-membered tetracyclic ether, corresponding to the EFGH-ring of gambierol and the BCDE-ring of gambieric acids, was efficiently accomplished via a two-directional approach. The key reactions were SMI2-induced double cyclization for construction of the F- and H-rings and SMI2-induced cyclization followed by ring expansion for construction of the E-ring.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available