AgNO2 as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines
摘要:
A straightforward method for synthesizing the pyrazole N-oxides from N-propargylamines and AgNO2, through oxidation/cyclization reaction had been developed. AgNO2, was used as the NO source for the first time to synthesize pyrazole N-oxides. Various substituted groups on N-propargylamines proceeded smoothly, and the desired products were obtained in good yields.
AgNO2 as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines
摘要:
A straightforward method for synthesizing the pyrazole N-oxides from N-propargylamines and AgNO2, through oxidation/cyclization reaction had been developed. AgNO2, was used as the NO source for the first time to synthesize pyrazole N-oxides. Various substituted groups on N-propargylamines proceeded smoothly, and the desired products were obtained in good yields.
Synthesis of 3-sulfonylquinolines by visible-light promoted metal-free cascade cycloaddition involving <i>N</i>-propargylanilines and sodium sulfinates
A visible-light promoted radical cascade reaction of N-propargylanilines with sodium sulfinates as sulfonyl radical precursors was developed under metal-free conditions.
Visible-light-induced multicomponent cascade cycloaddition involving <i>N</i>-propargyl aromatic amines, diaryliodonium salts and sulfur dioxide: rapid access to 3-arylsulfonylquinolines
作者:Deli Sun、Kun Yin、Ronghua Zhang
DOI:10.1039/c7cc09410h
日期:——
A visible-light-induced, Eosin Y catalyzed three-component synthesis of 3-arylsulfonylquinoline derivatives through N-propargyl aromatic amines, diaryliodonium salts and sulfurdioxide has been discovered. This transformation represents an efficient and attractive method for the straightforward synthesis of 3-arylsulfonylquinoline derivatives via the formation of C–S bonds and quinolines in one step
Electrooxidative tandem cyclization of <i>N</i>-propargylanilines with sulfinic acids for rapid access to 3-arylsulfonylquinoline derivatives
作者:Jie Liu、Min Wang、Laiqiang Li、Lei Wang
DOI:10.1039/d1gc00171j
日期:——
A series of N-propargylanilines (0.2 mmol) and sulfinic acids (0.5 mmol) afforded 3-arylsulfonylquinoline derivatives in high yields (70–93%) and low current efficiencies upon electrooxidation. Electrolyses were carried out in a one-compartment cell, under constant current and ambient conditions, in methanol-nBu4NBF4 containing pyridine (0.4 mmol), without any added chemical oxidant. A scale-up electrolysis
一系列N-炔丙基苯胺(0.2 mmol)和亚磺酸(0.5 mmol)以高收率(70-93%)和低电氧化效率提供了3-芳基磺酰基喹啉衍生物。在恒定电流和环境条件下,在单隔室的电解池中,在不添加任何化学氧化剂的,含有吡啶(0.4 mmol)的甲醇-n Bu 4 NBF 4中进行电解。在5mmol的N-炔丙基苯胺1a上进行放大电解,得到3-芳基磺酰基喹啉3aa,产率为65%,电流效率为56%。提出了机械学假说。
A visible-light-induced oxidative cyclization of <i>N</i>-propargylanilines with sulfinic acids to 3-sulfonated quinoline derivatives without external photocatalysts
作者:Yicheng Zhang、Wei Chen、Xueshun Jia、Lei Wang、Pinhua Li
DOI:10.1039/c8cc10235j
日期:——
A visible-light-induced oxidative cyclization of N-propargyl anilines with sulfinic acids was developed under external photocatalyst-free conditions. The reaction provides a straightforward route to 3-sulfonated quinoline derivatives with good functional group tolerance, excellent yields and high regio-selectivity.
Ag-Catalyzed or Ag/PPh<sub>3</sub>-Catalyzed Chemoselective Switchable Cascade Reactions of <i>N</i>-Propargyl Thiocarbamoyl Fluorides and Malonate Esters
作者:Zhongliang Cai、Junyi Zhou、Miao Yu、Liqin Jiang
DOI:10.1021/acs.orglett.1c03950
日期:2022.1.14
The divergent chemoselective synthesis of 2-methylene-2,3-dihydrothiazoles and 4-benzylidene pyrrolidine-2-thiones (most with E stereoselectivity) from N-propargyl thiocarbamoyl fluorides and malonate esters in moderate to excellent yields with a broad substrate scope and functional group tolerance has been accomplished. AgNTf2 catalyst at 60 °C in dichloroethane provided 4-benzylidene pyrrolidine-2-thiones
从N-炔丙基硫代氨基甲酰氟和丙二酸酯以中等至优异的产率,具有广泛的底物范围和功能性,不同的化学选择性合成 2-亚甲基-2,3-二氢噻唑和 4-亚苄基吡咯烷-2-硫酮(大多数具有 E 立体选择性)群体容忍度已经完成。AgNTf 2催化剂在 60 °C 下在二氯乙烷中提供 4-亚苄基吡咯烷-2-硫酮。AgOTf 催化剂和 PPh 3配体在回流乙腈中导致形成的 α,α-二酯硫代酰胺中间体的反应性发生完全转换,随后异构化得到 2-亚甲基-2,3-二氢噻唑。