Addition of dimethyloxosulfonium methylide to enantiomerically pure sulfinimines: Asymmetric synthesis of 2-substituted aziridines
FA Davis, P Zhou, CH Liang, RE Reddy
Index: Davis; Zhou; Liang; Reddy Tetrahedron Asymmetry, 1995 , vol. 6, # 7 p. 1511 - 1514
Full Text: HTML
Citation Number: 70
Abstract
Download full text in PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Diastereoselective addition of dimethyloxosulfonium methylide to chiral nonracemic pure sulfinimines 1 affords N-sulfinyl aziridines 3 in 58–70% de which are readily separated. The N-sulfinyl auxiliary in 3 was removed, without ring-opening, by treatment with MeLi.
Related Articles:
[Oppolzer, Wolfgang; Flaskamp, Elmar; Bieber, Lothar W. Helvetica Chimica Acta, 2001 , vol. 84, # 1 p. 141 - 145]
[Farmer, Jay J.; Attygalle, Athula B.; Smedley, Scott R.; Eisner, Thomas; Meinwald, Jerrold Tetrahedron Letters, 1997 , vol. 38, # 16 p. 2787 - 2790]