The development of an asymmetric Nicholas reaction using chiral phosphoramidite ligands
Journal article, 2008

An asymmetric version of the Nicholas reaction involving the use of chiral phosphoramidite ligands has been developed. Treatment of a cobalt carbonyl complexed propargylic alcohol with two equivalents of the chiral ligand, followed by reaction with a silyl enol ether in the presence of a Lewis acid, afforded, after decomplexation, the desired product in up to 74% ee for the carbon-carbon bond forming step. © Georg Thieme Verlag Stuttgart.

Author

N. Ljungdahl

Chalmers

N. P. Pera

Chalmers

K. H. O. Andersson

Chalmers

Nina Kann

Chalmers, Chemical and Biological Engineering, Organic Chemistry

Synlett

0936-5214 (ISSN) 1437-2096 (eISSN)

3 394-398

Subject Categories

Chemical Sciences

DOI

10.1055/s-2008-1032059

More information

Latest update

9/10/2018