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Rhodium‐Catalyzed Direct ortho C−H Thiolation of Cyclic N‐Sulfonyl Ketimines
Asian Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2020-02-12 , DOI: 10.1002/ajoc.202000017 Guangrui Shi 1 , Ruhima Khan 1 , Xuexin Zhang 1 , Yong Yang 2 , Yong Zhan 2 , Juan Li 2 , Yang Luo 2 , Baomin Fan 1, 3
Asian Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2020-02-12 , DOI: 10.1002/ajoc.202000017 Guangrui Shi 1 , Ruhima Khan 1 , Xuexin Zhang 1 , Yong Yang 2 , Yong Zhan 2 , Juan Li 2 , Yang Luo 2 , Baomin Fan 1, 3
Affiliation
An efficient method for the synthesis of thiolated cyclic N‐sulfonyl ketimines has been developed. The reaction proceeds via rhodium catalyzed C−H functionalization using disulfides in the presence of silver carbonate, silver triflate and copper acetate in toluene. The methodology showed broad substrate scope as a wide range of N‐sulfonyl ketimines participated in the reaction giving the thiolated products in up to 95%.
中文翻译:
铑催化的环N-磺酰基酮亚胺的直接邻位C H硫代反应
已开发出一种有效的合成硫醇化环状N-磺酰基酮亚胺的方法。反应在甲苯中存在碳酸银,三氟甲磺酸银和乙酸铜的情况下,使用二硫化物通过铑催化的CH官能化进行。该方法显示了广泛的底物范围,因为广泛的N-磺酰基酮亚胺参与了反应,使硫醇化产物的产率高达95%。
更新日期:2020-02-12
中文翻译:
铑催化的环N-磺酰基酮亚胺的直接邻位C H硫代反应
已开发出一种有效的合成硫醇化环状N-磺酰基酮亚胺的方法。反应在甲苯中存在碳酸银,三氟甲磺酸银和乙酸铜的情况下,使用二硫化物通过铑催化的CH官能化进行。该方法显示了广泛的底物范围,因为广泛的N-磺酰基酮亚胺参与了反应,使硫醇化产物的产率高达95%。