110010-05-4Relevant academic research and scientific papers
Pyridine Syntheses. II. Condensation Routes Toward Streptonigrin Ring C [1]
Robinson, J. Michael,Ahmed, Masood,Alaniz, Nicky J.,Boyles, Timothy P.,Brasher, Chris D.,Floyd, Kimberly A.,Holland, Preston L.,Maruffo, Laura D.,McMahan, Terry L.,Middleton, Stan,O'Hara, Kevin D.,Pack, Marcia J.,Reynolds, Brandon D.,Rodriquez, Romelia R.,Sawyer, Dennis E.,Sharp, Elena,Simpson, Sharai L.,Vanlandingham, Clint L.,Velasquez, Rebecca S.,Welch, Brian M.,Wright, C. David
, p. 65 - 69 (2007/10/03)
Alternative complimentary syntheses of penta-substituted pyridine rings with full regiochemical control of substituents were studied as a method for the synthesis of Streptonigrin (1). Various α-substituted acetophenones 2 were reacted with enones 3 in acetic acid/ammonium acetate and air to afford penta-substituted pyridines 4. α-Substituents that could provide a source of exocyclic nitrogen at position 3 of these Steptonigrin ring-C models proved to be the limiting factor. However, an inverse "3+2+1" cyclocondensation of α-cyanochalcone 5c with 2-furyl ethyl ketone (6b) afforded the desired model 6-(2-furyl)-5-methyl-2,4-diphenyl-3-pyridinecarbonitrile (4g) in 75% yield.
Electrolytic Reduction of Azidochalcones - Electrolytic Investigations on Vinyl Azides, VI.
Knittel, Dierk,Rao, V. Suryanarayana
, p. 1185 - 1193 (2007/10/02)
Cathodic reduction of α-azidochalcones under slightly protic conditions proves to be an excellent method for a selective conversion of the azido function to an amino group without affecting other reducible parts of the molecules.The amino-propenones retai
