ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CATALYSIS;
CATALYST;
DRUG STRUCTURE;
DRUG SYNTHESIS;
MICHAEL ADDITION;
MICROWAVE IRRADIATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
SOLID PHASE SYNTHESIS;
SUBSTITUTION REACTION;
CATALYSIS;
LEWIS ACIDS;
MICROWAVES;
MOLECULAR CONFORMATION;
PYRIDINES;
STEROIDS;
Synthesis of pyridine and dihydropyridine derivatives by regio- and stereoselective addition to N-activated pyridines
A.J. Bull, J.J. Mousseau, G. Pelletier, and B.A. Charectte Synthesis of pyridine and dihydropyridine derivatives by regio- and stereoselective addition to N-activated pyridines Chem Rev 112 2012 2642 2713
A metal-free decarboxylative cyclization from natural α-amino acids to construct pyridine derivatives
Q. Wang, C. Wan, Y. Gu, J. Zhang, L. Gao, and Z. Wang A metal-free decarboxylative cyclization from natural α-amino acids to construct pyridine derivatives Green Chem 13 2011 578 581
Steroidal heterocycles X1 steroidal [3,2-d] pyrimidines and related compounds
J.H. Ackerman, G.O. Potts, A.L. Beyler, and R.O. Clinton Steroidal heterocycles X1 steroidal [3,2-d] pyrimidines and related compounds J Med Chem 7 1964 238 240
Synthesis and structure of steroidal pregn-4-eno- and 5-pregnano[3,2-c]pyrazoles. A novel class of potent anti-inflammatory steroids
R. Hirschmann, P. Buchschacher, N.G. Steinberg, J.H. Fried, R. Ellis, and G.J. Kent Synthesis and structure of steroidal pregn-4-eno- and 5-pregnano[3,2-c]pyrazoles. A novel class of potent anti-inflammatory steroids J Am Chem Soc 86 1964 1520 1527
E-ring modified steroids as novel potent inhibitors of 17β- hydroxysteroid dehydrogenase type 1
DOI 10.1021/jm050348a
D.S. Fischer, G.M. Allan, C. Bubert, N. Vicker, A. Smith, and H.J. Tutill E-ring modified steroids as novel potent inhibitors of 17β-hydroxy steroid dehydrogenase type 1 J Med Chem 48 2005 5749 5770 (Pubitemid 41298348)
Anti-inflammatory profile of some synthesized heterocyclic pyridine and pyridine derivatives fused with steroidal structure
A.E. Amr, and M.M. Abdalla Anti-inflammatory profile of some synthesized heterocyclic pyridine and pyridine derivatives fused with steroidal structure Bioorg Med Chem 14 2006 4341 4352
Sequential amination/annulation/aromatization reaction of carbonyl compounds and propargylamine: A new one-pot approach to functionalized pyridines
DOI 10.1021/jo0347260
G. Abbiati, A. Arcadi, G. Bianchi, S. Di Giuseppe, F. Marinelli, and E. Rossi Sequential amination/annulation/aromatization reaction of carbonyl compounds and propargylamine: a new one-pot approach to functionalized pyridines J Org Chem 68 2003 6959 6966 (Pubitemid 37071775)
A microwave promoted solvent-free approach to steroidal quinolines and their in vitro evaluation for antimicrobial activities
S. Gogoi, K. Shekarrao, A. Duarah, T.C. Bora, S. Gogoi, and R.C. Boruah A microwave promoted solvent-free approach to steroidal quinolines and their in vitro evaluation for antimicrobial activities Steroids 77 2012 1438 1445
A revisit to the Hantzsch reaction: Unexpected products beyond 1,4-dihydropyridines
L. Shen, S. Cao, J. Wu, J. Zhang, H. Li, N. Liu, and X. Qian A revisit to the Hantzsch reaction: unexpected products beyond 1,4-dihydropyridines Green Chem 11 2009 1414 1420