39735-81-4Relevant academic research and scientific papers
Synthesis of β-chlorohydrins in water
Das, Biswanath,Venkateswarlu, Katta,Krishnaiah, Maddeboina
, p. 149 - 152 (2007/10/03)
2,4,6-Trichloro-1,3,5-triazine (TCT, cyanuric chloride) was found to mediate the regio- and stereoselective ring opening of epoxides in H 2O in the presence of morpholine at room temperature to afford the corresponding β-chlorohydrins in excellent yields (Table). The transformation is very simple, fast, efficient, and ecologically beneficial.
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 (2007/10/03)
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
