TY - JOUR
T1 - The aza-wharton reaction
T2 - Syntheses of cyclic allylic amines and vicinal hydroxyamines from the respective acylaziridines
AU - Silva, Saúl
AU - Rodrigues, Paula
AU - Bento, Isabel
AU - Maycock, Christopher D.
PY - 2015/3/20
Y1 - 2015/3/20
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84925352028&partnerID=8YFLogxK
U2 - 10.1021/jo5029387
DO - 10.1021/jo5029387
M3 - Article
AN - SCOPUS:84925352028
VL - 80
SP - 3067
EP - 3074
JO - Journal of Organic Chemistry
JF - Journal of Organic Chemistry
SN - 0022-3263
IS - 6
ER -