Enantiopure Eta(4)-(1-Sulfinyldiene)Iron(0) Tricarbonyl Complexes As Templates For Carbocycle Construction Via Ring-Closing Metathesis
Document Type
Article
Publication Date
2-10-2000
Published In
Organic Letters
Abstract
Enantiomerically pure 1-(1Z,3E)-sulfinyl iron(0) dienols have been elaborated to bis-olefins capable of undergoing ring-closing metathesis chemistry. Using Grubbs' ruthenium carbene catalyst, a six-membered carbocycle (with one chiral center) and seven-, eight-, and nine-membered carbocycles (with two chiral centers) have been prepared. Novel transformations include the LiClO4-promoted allylation of an alkylidene malonate and a reductive sulfur-carbon bond cleavage to convert a vinyl sulfoxide into an alkene with SmI2.
Recommended Citation
Robert S. Paley; Lara Ann Estroff , '97; Jean-Marc Gauguet , '98; Diana K. Hunt , '89; and Rebecca C. Newlin , '00.
(2000).
"Enantiopure Eta(4)-(1-Sulfinyldiene)Iron(0) Tricarbonyl Complexes As Templates For Carbocycle Construction Via Ring-Closing Metathesis".
Organic Letters.
Volume 2,
Issue 3.
365-368.
DOI: 10.1021/ol991311l
https://works.swarthmore.edu/fac-chemistry/74