Synthesis of louisianin C.
J Org Chem
; 68(12): 4970-2, 2003 Jun 13.
Article
in En
| MEDLINE
| ID: mdl-12790613
ABSTRACT
The synthesis of louisianin C (3), a member of a small family of 3,4,5-trisubstituted pyridyl natural products, is achieved in six steps and 11% overall yield starting from commercially available 3,5-dibromopyridine. The key step is a fluoride-induced desilylation-cyclization to afford carbinol 12.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Pyridines
/
Alkaloids
/
Allyl Compounds
Language:
En
Journal:
J Org Chem
Year:
2003
Document type:
Article
Affiliation country:
