Synthesis, spectral and antimicrobial evaluation of some novel 1-methyl-3-alkyl-2,6-diphenylpiperidin-4-one oxime carbonates.

[1]  H. V. Kumar,et al.  Synthesis, antioxidant and antimicrobial activity of novel vanillin derived piperidin-4-one oxime esters: preponderant role of the phenyl ester substituents on the piperidin-4-one oxime core. , 2012, Bioorganic & medicinal chemistry letters.

[2]  M. Shanmugam,et al.  Design, synthesis, spectral and biological evaluation of novel 1-allyl substituted 2,6-diphenylpiperidin-4-ones and its derivatives of oximes/oxime ethers. , 2012, Bioorganic & medicinal chemistry letters.

[3]  Sherine N. Khattab,et al.  Cyanoacetamide-based oxime carbonates: an efficient, simple alternative for the introduction of Fmoc with minimal dipeptide formation , 2012 .

[4]  V. Ramkumar,et al.  Synthesis, stereochemistry and antimicrobial studies of novel oxime ethers of aza/diazabicycles. , 2009, Bioorganic & medicinal chemistry letters.

[5]  V. Ramkumar,et al.  Synthesis, spectral, crystal and antimicrobial studies of biologically potent oxime ethers of nitrogen, oxygen and sulfur heterocycles. , 2009, Bioorganic & medicinal chemistry letters.

[6]  C. Ramalingan,et al.  Synthesis and study of antibacterial and antifungal activities of novel 8-methyl-7,9-diaryl-1,2,4,8-tetraazaspiro[4.5]decan-3-thiones. , 2005, European journal of medicinal chemistry.

[7]  A. Llebaria,et al.  A practical synthesis of carbamates using an ‘in-situ’ generated polymer-supported chloroformate , 2004 .

[8]  C. Ramalingan,et al.  Synthesis and study of antibacterial and antifungal activities of novel 1-[2-(benzoxazol-2-yl)ethoxy]- 2,6-diarylpiperidin-4-ones. , 2004, European journal of medicinal chemistry.

[9]  C. Ramalingan,et al.  Synthesis and Microbiological Evaluation of Novel [N-Acetyl-2,6-Diarylpiperidin-4-YL]-5-Spiro-4-Acetyl-2-(Acetylamino)-Δ2-1,3,4-Thiadiazolines , 2004, Medicinal Chemistry Research.

[10]  C. Ramalingan,et al.  Synthesis and microbiological evaluation of spiro piperidinyl heterocycles , 2003 .

[11]  C. Ramalingan,et al.  Synthesis and microbiological evaluation of benzimidazolylethoxypiperidones , 2003 .

[12]  K. W. Jung,et al.  Perspectives on Alkyl Carbonates in Organic Synthesis , 2000 .

[13]  B. Vergani,et al.  A New Simple One-Pot Regioselective Preparation of Mixed Diesters of Carbonic Acid. , 1998, The Journal of organic chemistry.

[14]  H. Meshram,et al.  Zinc promoted simple and convenient synthesis of carbamates: An easy access for amino group protection , 1998 .

[15]  C. Ghiron,et al.  The stereoselective synthesis of 4-formyltrinem, a key intermediate for novel trinems , 1997 .

[16]  P. Majer,et al.  A safe and efficient method for preparation of N,N'-unsymmetrically disubstituted ureas utilizing triphosgene , 1994 .

[17]  M. Roof,et al.  A safe and efficient method for conversion of 1,2- and 1,3-diols to cyclic carbonates utilizing triphosgene , 1993 .

[18]  S. Pelletier.  Alkaloids: Chemical and Biological Perspectives , 1992, Alkaloids: Chemical and Biological Perspectives.

[19]  E. Giralt,et al.  Piperidine: Structure, Preparation, Reactivity, and Synthetic Applications of Piperidine and its Derivatives , 1991 .

[20]  S. Pelletier.  Alkaloids: Chemical and Biological Perspectives , 1991, Alkaloids: Chemical and Biological Perspectives.

[21]  A. Katritzky,et al.  The chemistry of benzotriazole. A novel and versatile synthesis of 1-alkyl-, 1-aryl-, 1-(alkylamino)-, or 1-amido-substituted and of 1,2,6-trisubstituted piperidines from glutaraldehyde and primary amines or monosubstituted hydrazines , 1990 .

[22]  G. Grynkiewicz,et al.  The synthesis of mixed carbonates from alcohols, dialkyl azodicarboxylate and tris(dimethylamino)-phosphine , 1975 .

[23]  E. May,et al.  Agonists--antagonists derived from desomorphine and metopon. , 1970, Journal of medicinal chemistry.

[24]  M. Balasubramanian,et al.  Studies on conformation—I : Preparation and stereochemistry of some 4-piperidinols , 1963 .

[25]  C. Noller,et al.  The preparation of some piperidine derivatives by the Mannich reaction. , 1948, Journal of the American Chemical Society.