416841-46-8Relevant academic research and scientific papers
The aza-wharton reaction: Syntheses of cyclic allylic amines and vicinal hydroxyamines from the respective acylaziridines
Silva, Saúl,Rodrigues, Paula,Bento, Isabel,Maycock, Christopher D.
, p. 3067 - 3074 (2015)
The Wharton reaction, initially described for acyl epoxides, has been studied using the structurally similar aziridines. By this reaction, a range of cyclic allylic amines and vicinal amino alcohols have been prepared stereoselectively and, in some cases, enantiomerically pure.
Radical Cyclisations of Dienes and Enynes using Phosphorus- and Sulfur-Centered Radicals
Brumwell, Julie E.,Simpkins, Nigel S.,Terrett, Nicholas K.
, p. 13533 - 13552 (2007/10/02)
Reaction of a number of 1,6-diene or enyne systems with TolSO2SePh, under free radical conditions, results in selenosulfonylation with concomitant C-C bond formation, to give cyclised alkyl or vinyl sulfones containing the synthetically useful phenylselen
