Journal of heterocyclic chemistry

N??acyl and N??alkoxycarbonyl derivatives of 1H??1, 2, 3??triazolo??[4, 5??c] pyridine; Preparation and application

J Holt, A Fiksdahl

Index: Holt, Jarle; Fiksdahl, Anne Journal of Heterocyclic Chemistry, 2006 , vol. 43, # 2 p. 417 - 423

Full Text: HTML

Citation Number: 6

Abstract

Some substituted 1, 2, 3-triazolopyridines (1, 2) are analgesic, antipyretic, antiasthmatic or useful as inflammation inhibitors [1, 2] while others have been patented for their anxiolytic antidepressant properties [3] and herbicidal activity [4]. The 1, 2, 3-triazolo [4, 5-c] pyridine (1) is a commercially available fine chemical, but to our knowledge, only to a very high price. Substituted 1, 2, 3-triazolopyridines (1, 2) have previously been prepared by amine ...

~73%

~77%

~73%

~72%

~85%

~0%

~0%

~0%

~0%

~0%

~0%

~0%

~0%

~0%

~0%

~10%

~73%

~70%

~71%

Direct reductive amination using triethylsilane and catalyti...

[Matsumura, Takehiko; Nakada, Masahisa Tetrahedron Letters, 2014 , vol. 55, # 10 p. 1829 - 1834]

N-substituted carbamates syntheses with alkyl carbamates as ...

[Shang, Jianpeng; Guo, Xiaoguang; Shi, Feng; Ma, Yubo; Zhou, Feng; Deng, Youquan Journal of Catalysis, 2011 , vol. 279, # 2 p. 328 - 336]

Electrochemically promoted CN bond formation from amines and...

[Feroci; Orsini; Rossi; Sotgiu; Inesi Journal of Organic Chemistry, 2007 , vol. 72, # 1 p. 200 - 203]

Catalytic activity of MCM-41–TBD in the selective preparatio...

[Carloni, Silvia; De Vos, Dirk E.; Jacobs, Pierre A.; Maggi, Raimondo; Sartori, Giovanni; Sartorio, Raffaella Journal of Catalysis, 2002 , vol. 205, # 1 p. 199 - 204]

Nucleophilic Attack vs. General Base Assisted Hydrolysis in ...

[King, James F.; Guo, Zhen Rong; Klassen, Darryl F. Journal of Organic Chemistry, 1994 , vol. 59, # 5 p. 1095 - 1101]