Reactions of 2-substituted epichlorohydrins

1996-01-01
Tanyeli, Cihangir
Demir, AS
Akhmedov, IM
Ozgul, E
Kandemir, CG
2-Substituted epichlorohydrins have been synthesized by starting with 1,2-dichloro acetone and various alkyl and aryl halides via dichlorohydrins followed by cyclization. The reactive 2-substituted epichlorohydrins were subjected to nucleophilic attacking of azide and cyanide ions to afford corresponding beta-azido alcohols and alpha,beta-unsaturated nitriles.

Citation Formats
C. Tanyeli, A. Demir, I. Akhmedov, E. Ozgul, and C. Kandemir, “Reactions of 2-substituted epichlorohydrins,” SYNTHETIC COMMUNICATIONS, vol. 26, no. 16, pp. 2967–2980, 1996, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/38327.