108167-42-6Relevant articles and documents
ASYMMETRIC EPOXIDATION OF NONFUNCTIONALIZED ALKENES WITH HIGH ENANTIOSELECTIVITY USING CHIRAL SULFAMYLOXAZIRIDINES
Davis, Franklin A.,Chattopadhyay, Sankar
, p. 5079 - 5082 (1986)
High enantioselectivities (19-65percent ee) are reported for the asymmetric epoxidation of a series of nonfunctionalized alkenes using chiral sulfamyloxaziridines (1b/2b).
Chemistry of Oxaziridines. 8. Asymmetric Oxidation of Nonfunctionalized Sulfides to Sulfoxides with High Enantioselectivity by 2-Sulfamyloxaziridines. The Influence of the Oxaziridine C-Aryl Group on the Asymmetric Induction
Davis, Franklin A.,McCauley, John P.,Chattopadhyay, Sankar,Harakal, Mark E.,Towson, James C.,et al.
, p. 3370 - 3377 (2007/10/02)
Chiral sulfamyloxaziridines 6 and 7, prepared by biphasic oxidation of the corresponding sulfamylimines 5, afford high asymmetric induction for the oxidation of a series of nonfunctionalized sulfides to sulfoxides (53-91percent ee).The enantioselectivitie