BF3· OEt2-Mediated highly regioselective SN2-type ring-opening of N-activated aziridines and N-activated azetidines by tetraalkylammonium halides
MK Ghorai, A Kumar, DP Tiwari
Index: Ghorai, Manas K.; Kumar, Amit; Tiwari, Deo Prakash Journal of Organic Chemistry, 2010 , vol. 75, # 1 p. 137 - 151
Full Text: HTML
Citation Number: 70
Abstract
A highly regioselective Lewis acid-mediated SN2-type ring-opening of N-sulfonylaziridines and azetidines with tetraalkylammonium halides in CH2Cl2 solution to afford 1, 2-and 1, 3- haloamines in excellent yields is described. An easy diastereoselective route toward substituted chiral N-tosylaziridines has been developed. The mechanism of ring-opening via SN2 pathway has been confirmed by the formation of chiral haloamines with excellent er ...
Related Articles:
[Barn; Caulfield; Cottney; McGurk; Morphy; Rankovic; Roberts Bioorganic and Medicinal Chemistry, 2001 , vol. 9, # 10 p. 2609 - 2624]
[Das, Biswanath; Reddy, Parigi Raghavendar; Sudhakar, Chithaluri; Lingaiah, Maram Tetrahedron Letters, 2011 , vol. 52, # 27 p. 3521 - 3522]
[Shi, Wei; Bai, Chun-Mei; Zhu, Kai; Cui, Dong-Mei; Zhang, Chen Tetrahedron, 2014 , vol. 70, # 2 p. 434 - 438]
[Alexander, Michael D.; Anderson, Robert E.; Sisko, Joseph; Weinreb, Steven M. Journal of Organic Chemistry, 1990 , vol. 55, # 8 p. 2563 - 2564]
[Stamm, Helmut; Onistschenko, Andreas; Buchholz, Berthold; Mall, Thomas Journal of Organic Chemistry, 1989 , vol. 54, # 1 p. 193 - 199]