Nucleophilic substitution reactions of heterocyclic amines and acyclic diamines with chlorofluoro olefins and hexafluoropropylene oxide
摘要:
The reactions of CH3N(H)CH2CH2N(H)CH3, CH3N(H)CH2CH2CH2N(H)CH3, and the cyclic amines piperazine, N-phenylpiperazine, and N-methylpiperazine with both cyclic and acyclic 1,2-dichloroperfluoroolefins are reported. Nucleophilic attack occurs at olefinic carbon, followed, in some cases, by cyclization and beta-elimination A variety of unusual polyfluorinated tertiary amines and heterocycles are synthesized.
Mir Qui-Chee, Guo Cai-Yun, Kirchmeier Robert L., Shreeve Jeanne M., J. Org. Chem, 59 (1994) N 1, S 173-177
作者:Mir Qui-Chee, Guo Cai-Yun, Kirchmeier Robert L., Shreeve Jeanne M.
DOI:——
日期:——
Nucleophilic substitution reactions of heterocyclic amines and acyclic diamines with chlorofluoro olefins and hexafluoropropylene oxide
作者:Qui Chee Mir、Cai Yun Guo、Robert L. Kirchmeier、Jean'ne M. Shreeve
DOI:10.1021/jo00080a028
日期:1994.1
The reactions of CH3N(H)CH2CH2N(H)CH3, CH3N(H)CH2CH2CH2N(H)CH3, and the cyclic amines piperazine, N-phenylpiperazine, and N-methylpiperazine with both cyclic and acyclic 1,2-dichloroperfluoroolefins are reported. Nucleophilic attack occurs at olefinic carbon, followed, in some cases, by cyclization and beta-elimination A variety of unusual polyfluorinated tertiary amines and heterocycles are synthesized.