Publications

Gold(III) chloride promoted addition of electron-rich heteroaromatic compounds to the C=C and C=O bonds of enals

Gold(III) chloride promoted addition of electron-rich heteroaromatic compounds to the C=C and C=O bonds of enals

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Vidya, N; Abhilash, KG
  • Volume :
  • Year : 2006
An efficient multicomponent protocol for the stereoselective synthesis of oxazinobenzothiazole derivatives

An efficient multicomponent protocol for the stereoselective synthesis of oxazinobenzothiazole derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Pillai A.N., Rema Devi B., Suresh E., Nair V.
  • Volume :
  • Year : 2007
Sterically encumbered regioselective cycloaddition of a calixarene derived bis(spirodienone) with 1,2-benzoquinones

Sterically encumbered regioselective cycloaddition of a calixarene derived bis(spirodienone) with 1,2-benzoquinones

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Varma, RL; Ganga, VB; Suresh, E; Suresh, CH
  • Volume :
  • Year : 2006
A facile and efficient stereoselective synthesis of highly functionalized trisubstituted alkene derivatives of ferrocenealdehyde

A facile and efficient stereoselective synthesis of highly functionalized trisubstituted alkene derivatives of ferrocenealdehyde

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Shanmugam, P; Vaithiyanathan, V; Viswambharan, B; Madhavan, S
  • Volume :
  • Year : 2007
An efficient synthesis of isothiazolidines via sulfonium ylides formed by the reaction of thietanes and nitrene

An efficient synthesis of isothiazolidines via sulfonium ylides formed by the reaction of thietanes and nitrene

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Nair, SM; Devipriya, S; Sethumadhavan, D
  • Volume :
  • Year : 2006
Efficient synthesis of [1,3]oxazino[2,3-a]quinoline derivatives by a novel 1,4-dipolar cycloaddition involving a quinoline-DMAD zwitterion and carbonyl compounds

Efficient synthesis of [1,3]oxazino[2,3-a]quinoline derivatives by a novel 1,4-dipolar cycloaddition involving a quinoline-DMAD zwitterion and carbonyl compounds

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Devipriya, S; Eringathodi, S
  • Volume :
  • Year : 2007
Reaction of TPP-azodicarboxylate zwitterions and aryl aldehydes: unprecedented synthesis of acyl carbamates

Reaction of TPP-azodicarboxylate zwitterions and aryl aldehydes: unprecedented synthesis of acyl carbamates

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Mathew, SC; Biju, AT; Suresh, E
  • Volume :
  • Year : 2007
Analogues of the Quararibea metabolite chiral enolic-gamma-lactone from (2S,3S)- and (2S,3R)-tetrahydro-3-hydroxy-5-oxo-2,3-furandicarboxylic acids

Analogues of the Quararibea metabolite chiral enolic-gamma-lactone from (2S,3S)- and (2S,3R)-tetrahydro-3-hydroxy-5-oxo-2,3-furandicarboxylic acids

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Gopinath, C; Thomas, S; Nair, MS; Ibnusaud, I
  • Volume :
  • Year : 2006
A novel reaction of vicinal tricarbonyl compounds with the isocyanide-DMAD zwitterion: formation of highly substituted furan derivatives

A novel reaction of vicinal tricarbonyl compounds with the isocyanide-DMAD zwitterion: formation of highly substituted furan derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Deepthi, A
  • Volume :
  • Year : 2006
Stereoselective synthesis of 3,4-trans-disubstituted pyrrolidines and cyclopentanes via intramolecular radical cyclizations mediated by CAN

Stereoselective synthesis of 3,4-trans-disubstituted pyrrolidines and cyclopentanes via intramolecular radical cyclizations mediated by CAN

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Mohanan, K; Suja, TD; Suresh, E
  • Volume :
  • Year : 2006