Publications

Engaging the pyridine-DMAD Zwitterion in a novel strategy for the selective synthesis of highly substituted benzene and cyclopentenedione derivatives

Engaging the pyridine-DMAD Zwitterion in a novel strategy for the selective synthesis of highly substituted benzene and cyclopentenedione derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Pillai, AN; Beneesh, PB; Suresh, E
  • Volume :
  • Year : 2005
Reaction of Huisgen zwitterion with 1,2-benzoquinones and isatins: Expeditious synthesis of dihydro-1,2,3-benzoxadiazoles and spirooxadiazolines

Reaction of Huisgen zwitterion with 1,2-benzoquinones and isatins: Expeditious synthesis of dihydro-1,2,3-benzoxadiazoles and spirooxadiazolines

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Biju, AT; Vinod, AU; Suresh, E
  • Volume :
  • Year : 2005
Reaction of diaryl-1,2-diones with triphenylphosphine and diethyl azodicarboxylate leading to N,N-dicarboethoxy monohydrazones via a novel rearrangement

Reaction of diaryl-1,2-diones with triphenylphosphine and diethyl azodicarboxylate leading to N,N-dicarboethoxy monohydrazones via a novel rearrangement

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Biju, AT; Abhilash, KG; Menon, RS; Suresh, E
  • Volume :
  • Year : 2005
Practical synthesis of triaryl and triheteroarylmethanes by reaction of aldehydes and activated arenes promoted by gold(III) chloride

Practical synthesis of triaryl and triheteroarylmethanes by reaction of aldehydes and activated arenes promoted by gold(III) chloride

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Abhilash, KG; Vidya, N
  • Volume :
  • Year : 2005
Pyridine-catalyzed addition of diaryl-1,2-diones to dimethyl butynedioate leading to the formation of 1,2-diaroyl dimethyl maleates via an unprecedented rearrangementt

Pyridine-catalyzed addition of diaryl-1,2-diones to dimethyl butynedioate leading to the formation of 1,2-diaroyl dimethyl maleates via an unprecedented rearrangementt

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Pillai, AN; Menon, RS; Suresh, E
  • Volume :
  • Year : 2005
Synthesis of a novel cyclic donor-acceptor conjugate for selective recognition of ATP

Synthesis of a novel cyclic donor-acceptor conjugate for selective recognition of ATP

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Neelakandan, PP; Hariharan, M; Ramaiah, D
  • Volume :
  • Year : 2005
Modified (22 pi) smaragdyrins with large two-photon absorption cross section: A structure function correlation

Modified (22 pi) smaragdyrins with large two-photon absorption cross section: A structure function correlation

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Misra, R; Kumar, R; Chandrashekar, TK; Nag, A; Goswami, D
  • Volume :
  • Year : 2006
Effect of meso aryl substituents on the synthesis of core-modified expanded porphyrins

Effect of meso aryl substituents on the synthesis of core-modified expanded porphyrins

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Kumar, R; Misra, R; Chandrashekar, TK
  • Volume :
  • Year : 2006
Synthesis of new cholesterol- and sugar-anchored squaraine dyes: Further evidence of how electronic factors influence dye formation

Synthesis of new cholesterol- and sugar-anchored squaraine dyes: Further evidence of how electronic factors influence dye formation

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Jyothish, K; Avirah, RR; Ramaiah, D
  • Volume :
  • Year : 2006
Two unprecedented multicomponent reactions involving N-heterocyclic carbenes, activated acetylenes, and aldehydes

Two unprecedented multicomponent reactions involving N-heterocyclic carbenes, activated acetylenes, and aldehydes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Sreekumar, V; Bindu, S; Suresh, E
  • Volume :
  • Year : 2005