| Literature DB >> 12688748 |
Daniel J Weix1, Jonathan A Ellman.
Abstract
[reaction: see text] An improved synthesis of tert-butanesulfinamide that overcomes the scalability problems of the previous syntheses is described. The key step is the catalytic asymmetric oxidation of the inexpensive di-tert-butyl disulfide starting material. The new homogeneous reaction conditions utilize an inexpensive chiral ligand prepared in a single step from commercially available cis-1-amino-indan-2-ol. The reaction is performed at a 2.3 M concentration in the practical solvent acetone and can readily be run on a kilogram scale.Entities:
Year: 2003 PMID: 12688748 DOI: 10.1021/ol034254b
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005