Reactions of 2-substituted epichlorohydrins

1996-01-01
Tanyeli, Cihangir
Akhmedov, IM
Ozgul, E
Kandemir, CG
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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.
Organic Chemistry
https://hdl.handle.net/11511/38327
SYNTHETIC COMMUNICATIONS
Department of Chemistry, Article

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Citation Formats
C. Tanyeli, I. Akhmedov, E. Ozgul, and C. Kandemir, “Reactions of 2-substituted epichlorohydrins,” SYNTHETIC COMMUNICATIONS, pp. 2967–2980, 1996, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/38327.
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