79026-62-3Relevant academic research and scientific papers
Cyclosulfamide as a chiral auxiliary: Application to efficient asymmetric synthesis (alkylation/aldolization)
Fecourt, Fabien,Lopez, Gerald,Lee, Arie Van Der,Martinez, Jean,Dewynter, Georges
experimental part, p. 2361 - 2366 (2010/12/20)
The chiral cyclosulfamide (S)-2-benzyl-4-isopropyl-1,2,5-thiadiazolidine 1,1-dioxide was designed as a chimera of Evans and Oppolzer chiral auxiliaries. The N-propionyl derivative appeared to be very powerful for the stereocontrolled synthesis of chiral building blocks through asymmetric aldolization and alkylation reactions.
Synthesis of a new fluorinated oxazolidinone and its reactivity as a chiral auxiliary in Aldol reactions
Fustero, Santos,Piera, Julio,Sanz-Cervera, Juan F.,Bello, Paula,Mateu, Natalia
, p. 647 - 653 (2008/01/06)
A new enantiomerically pure fluorinated oxazolidinone has been prepared from a fluorinated imidoyl chloride and an optically pure sulfoxide. The diastereoselective reduction of the β-iminosulfoxide thus formed followed by elimination of the sulfoxide and
