17798-13-9Relevant articles and documents
Regio- and stereoselective ring opening of epoxides and aziridines using zirconyl chloride: An efficient approach for the synthesis of β-chlorohydrins and β-chloroamines
Das, Biswanath,Krishnaiah, Maddeboina,Venkateswarlu, Katta
, p. 82 - 83 (2007)
Zirconyl chloride mediated regio- and stereoselective ring opening of epoxides and aziridines at room temperature affords the corresponding β-chlorohydrins and β-chloroamines, respectively in high yields. Copyright
Unprecedented CO2-promoted aminochlorination of olefins with Chloramine-T
Minakata, Satoshi,Yoneda, Yoshimi,Oderaotoshi, Yoji,Komatsu, Mitsuo
, p. 967 - 969 (2006)
A new synthetic procedure for the aminochlorination of olefins for the synthesis of vicinal chloroamine derivatives using a combination of Chloramine-T and carbon dioxide is described. The method can be applied to a variety of olefins, including an electr
Regioselective ring opening of aziridines with activated DMF complexes: A facile synthesis of β-haloamines
Pandey, Manoj K.,Bisai, Alakesh,Singh, Vinod K.
, p. 9661 - 9663 (2004)
A wide variety of aziridines were converted to the corresponding β-haloamines using activated DMF complexes in good to excellent yields with high regioselectivity.
Use of trichloroacetonitrile as a hydrogen chloride generator for ring-opening reactions of aziridines
Toda, Yasunori,Matsuda, Riki,Gomyou, Shuto,Suga, Hiroyuki
supporting information, p. 3825 - 3829 (2019/04/17)
Regioselective ring-opening reactions of 2-aryl-N-tosylaziridines are described, in which hydrogen chloride is generated by photodegradation of trichloroacetonitrile. HCl adducts are obtained in high yields in 1,4-dioxane, whereas methanol adducts are pre
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