1021372-74-6Relevant articles and documents
Metal-free synthesis of sulfonamides via iodine-catalyzed oxidative coupling of sulfonyl hydrazides and amines
Parumala, Santosh Kumar Reddy,Peddinti, Rama Krishna
supporting information, p. 1232 - 1235 (2016/03/01)
A novel, rapid, and environmentally-friendly protocol for the synthesis of sulfonamides using iodine as catalyst under solvent-free conditions is described. This method involves the oxidative coupling of sulfonyl hydrazides and amines in the presence of catalytic amount of iodine using TBHP as oxidant. This protocol does not require purification techniques such as column chromatography and recrystalization.
Synthesis of 1,2,4-trisubstituted-1,2,5,6-tetrahydropyridines
Chang, Meng-Yang,Lee, Ming-Fang,Lee, Nien-Chia,Huang, Yu-Ping,Lin, Chung-Han
scheme or table, p. 588 - 591 (2011/03/18)
A novel method for the synthesis of 1,2,4-trisubstituted- or 1,2,3,4-tetrasubstituted-1,2,5,6-tetrahydropyridine is presented. The process was carried out by the bromomethoxylation of 4-substituted-1,2,5,6- tetrahydropyridines 1 with N-bromosuccinimide (NBS) in methanol, dehydrobromination with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), and boron trifluoride etherate (BF3-OEt2)-catalyzed cross coupling of the corresponding enamine with trimethylsilyl-based nucleophiles. Homokainoid analogs were also synthesized via the protocol.