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Three-component difluoroalkylation and trifluoromethylthiolation/trifluoromethylselenolation of π-bonds
Chemical Communications ( IF 4.3 ) Pub Date : 2018-01-09 00:00:00 , DOI: 10.1039/c7cc09083h Bo-Sheng Zhang 1, 2, 3, 4 , Lu-Yao Gao 1, 2, 3, 4 , Zhe Zhang 1, 2, 3, 4 , Yu-Hua Wen 1, 2, 3, 4 , Yong-Min Liang 1, 2, 3, 4
Chemical Communications ( IF 4.3 ) Pub Date : 2018-01-09 00:00:00 , DOI: 10.1039/c7cc09083h Bo-Sheng Zhang 1, 2, 3, 4 , Lu-Yao Gao 1, 2, 3, 4 , Zhe Zhang 1, 2, 3, 4 , Yu-Hua Wen 1, 2, 3, 4 , Yong-Min Liang 1, 2, 3, 4
Affiliation
This report describes a new method for three-component difluoroalkylation and trifluoromethylthiolation/trifluoromethylselenolation of π-bonds via air-stable SCF3 and SeCF3 reagents as free-radical initiators of ethyl iododifluoroacetate. β-Proton elimination can be overcome effectively in this reaction system, and a broad substrate scope, including alkenes and alkynes, makes this approach practical and attractive.
中文翻译:
π键的三组分二氟烷基化和三氟甲基硫醇化/三氟甲基硒化
该报告描述了一种新的方法,该方法通过空气稳定的SCF 3和SeCF 3试剂作为碘代二氟乙酸乙酯的自由基引发剂,对三键进行三组分二氟烷基化和三氟甲基硫醇化/三氟甲基硒化。在该反应系统中可以有效克服β-质子的消除,并且广泛的底物范围(包括烯烃和炔烃)使该方法实用且有吸引力。
更新日期:2018-01-31
中文翻译:
π键的三组分二氟烷基化和三氟甲基硫醇化/三氟甲基硒化
该报告描述了一种新的方法,该方法通过空气稳定的SCF 3和SeCF 3试剂作为碘代二氟乙酸乙酯的自由基引发剂,对三键进行三组分二氟烷基化和三氟甲基硫醇化/三氟甲基硒化。在该反应系统中可以有效克服β-质子的消除,并且广泛的底物范围(包括烯烃和炔烃)使该方法实用且有吸引力。