142598-62-7Relevant articles and documents
A facile regioselective ring opening of aziridines to haloamines using tetrabutylammonium halides in the presence of β-cyclodextrin in water
Narender,Surendra,Krishnaveni, N. Srilakshmi,Reddy, M. Somi,Rao, K. Rama
, p. 7995 - 7997 (2004)
A variety of N-tosylaziridines undergo regioselective ring opening with tetrabutylammonium halides in the presence of β-cyclodextrin in water at pH 4 and room temperature to afford the corresponding haloamines in excellent yields.
Indium trihalide mediated regioselective ring opening of aziridines: A facile synthesis of 2-haloamines
Yadav,Subba Reddy,Mahesh Kumar
, p. 1417 - 1418 (2001)
A variety of N-tosyl aziridines undergo ring opening with indium trihalides in acetonitrile at ambient temperature to afford the corresponding haloamines in excellent yields with high regioselectivity.
Use of allylzinc halide as a source of halide: Differential addition of nucleophiles to Ts-aziridines and aldehydes under similar reaction conditions
Chatterjee, Rana,Samanta, Satyajit,Mukherjee, Anindita,Santra, Sougata,Zyryanov, Grigory V.,Majee, Adinath
supporting information, p. 276 - 283 (2019/01/04)
We have observed that the allylic zinc halide under identical reaction conditions acts in different modes for different electrophiles. For Ts-aziridines the halide part of the allylic halide has been introduced as a nucleophile and for the carbonyl compou
Regioselective (Diacetoxyiodo)benzene-promoted halocyclization of unfunctionalized olefins
Liu, Gong-Qing,Li, Yue-Ming
, p. 10094 - 10109 (2015/02/19)
A metal-free method for intramolecular halocyclization of unfunctionalized olefins was detailed. (Diacetoxyiodo)benzene (PIDA) was very effective for haloamidation, haloetherification, and halolactonization of unfunctionalized olefins. In the presence of
