Exceptionally easy ring cleavage of benzimidazoles by α,β- acetylenic γ-hydroxy nitriles and water

Synthesis

Volumn , Issue 9, 2010, Pages 1536-1542

  Trofimov, Boris A ^a   Andriyankova, Ludmila V ^a   Nikitina, Lina P ^a   Belyaeva, Kseniya V ^a   Mal'kina, Anastasiya G ^a   Afonin, Andrei V ^a  

^a A E FAVORSKY IRKUTSK INSTITUTE OF CHEMISTRY   (Russian Federation)

Author keywords

Alkynes; Benzimidazoles; Heterocycles; Multicomponent reactions; Nitriles; Polycycles; Ring opening

Indexed keywords

BENZIMIDAZOLES; HETEROCYCLES; MULTI-COMPONENT REACTIONS; POLYCYCLES; RING OPENING;

ACETONITRILE; ACETYLENE; AMIDES; SYNTHESIS (CHEMICAL);

CYANIDES;

[2 [(5 AMINOFURAN 3(2H)YLIDENE)AMINO]PHENYL]FORMAMIDE; ACETONITRILE; ACETYLENE; ALPHA,BETA ACETYLENIC GAMMA HYDROXYNITRILE; AMPHOLYTE; BENZIMIDAZOLE DERIVATIVE; FORMAMIDE DERIVATIVE; IMIDAZOLE; NITRILE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CRYSTAL STRUCTURE; ISOMERIZATION; NUCLEAR OVERHAUSER EFFECT; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; ROOM TEMPERATURE; X RAY ANALYSIS;

EID: 77955347422     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/S-0029-1218704     Document Type: Article

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