Journal
ORGANIC LETTERS
Volume 15, Issue 14, Pages 3714-3717Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol401582e
Keywords
-
Categories
Funding
- European Research Council under the European Union's Seventh Framework Programme/ERC [277588]
Ask authors/readers for more resources
Conversion of a simple furan into the intact erythrinane skeleton in one synthetic operation has been accomplished. The one-pot reaction sequence begins with singlet oxygen photooxygenation of the furan and proceeds via a 2-pyrrolidinone formation, cyclization of the pendant aldehyde moiety and an N-acyliminium ion formation and terminates with a Pictet-Spengler-type aromatic substitution. The method has been used to achieve a rapid and highly effective formal synthesis of erysotramidine.
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