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Stereocontrolled synthesis of novel spirocyclic oxa-bridged cyclooetanoids through sequential transformations of pentafulvenes

Stereocontrolled synthesis of novel spirocyclic oxa-bridged cyclooetanoids through sequential transformations of pentafulvenes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Krishnan, KS; Kuthanappillil, JM; John, J; Suresh, CH; Suresh, E; Radhakrishnan, KV
  • Volume :
  • Year : 2008
An efficient three-component reaction involving triazolylidene carbene, DMAD, and aldehydes for the synthesis of furanone derivatives

An efficient three-component reaction involving triazolylidene carbene, DMAD, and aldehydes for the synthesis of furanone derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Mathew, SC; Vellalath, S; Pillai, AN; Suresh, E
  • Volume :
  • Year : 2008
Periselectivity in the cycloaddition reactions of pentafulvenes with 3-oxidopyrylium betaines: Effect of substituent on the C-6 carbon

Periselectivity in the cycloaddition reactions of pentafulvenes with 3-oxidopyrylium betaines: Effect of substituent on the C-6 carbon

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Krishnan, KS; Rajan, R; Radhakrishnan, KV
  • Volume :
  • Year : 2008
N-heterocyclic carbene catalyzed reaction of enals and diaryl-1,2 diones via homoenolate: Synthesis of 4,5,5-trisubstituted gamma-butyrolactones

N-heterocyclic carbene catalyzed reaction of enals and diaryl-1,2 diones via homoenolate: Synthesis of 4,5,5-trisubstituted gamma-butyrolactones

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Vellalath, S; Poonoth, M; Suresh, E; Viji, S
  • Volume :
  • Year : 2007
Efficient condensation reactions of electron-rich arenes with aldehydes and enals promoted by gold(III) chloride: Practical synthesis of triaryl- and triheteroarylmethanes and related compounds

Efficient condensation reactions of electron-rich arenes with aldehydes and enals promoted by gold(III) chloride: Practical synthesis of triaryl- and triheteroarylmethanes and related compounds

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Vidya, N; Abhilash, KG
  • Volume :
  • Year : 2006
Novel pyridine-catalyzed reaction of dimethyl acetylenedicarboxylate with aldehydes and N-tosylimines: Efficient synthesis of 2-benzoylfumarates and 1-azadienes

Novel pyridine-catalyzed reaction of dimethyl acetylenedicarboxylate with aldehydes and N-tosylimines: Efficient synthesis of 2-benzoylfumarates and 1-azadienes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Sreekanth, AR; Abhilash, N; Biju, AT; Devi, BR; Menon, RS; Rath, NP; Srinivas, R
  • Volume :
  • Year : 2003
Chemoselective 1,3-dipolar cycloaddition reactions of rhodium(II)-generated isomunchnones with 1,4-quinones: Synthesis of novel azapolycycles

Chemoselective 1,3-dipolar cycloaddition reactions of rhodium(II)-generated isomunchnones with 1,4-quinones: Synthesis of novel azapolycycles

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Santhi, V; Sheela, KC; Radhakrishnan, KV; Rath, NP
  • Volume :
  • Year : 2003
[4+1] cycloaddition reactions of o-thioquinones with isocyanides: Novel syntheses of 2-imino-1,3-oxathioles

[4+1] cycloaddition reactions of o-thioquinones with isocyanides: Novel syntheses of 2-imino-1,3-oxathioles

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Mathew, B; Vinod, AU; Mathen, JS; Ros, S; Menon, RS; Varma, RL; Srinivas, R
  • Volume :
  • Year : 2003
Indium-mediated allylation and propargylation of isatins: A facile synthesis of 3-substituted 3-hydroxyoxindoles

Indium-mediated allylation and propargylation of isatins: A facile synthesis of 3-substituted 3-hydroxyoxindoles

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Ros, S; Jayan, CN; Viji, S
  • Volume :
  • Year : 2003
Lewis acid catalyzed addition of allylsilane to o-quinonediimides: Formal Diels-Alder reaction versus allylation

Lewis acid catalyzed addition of allylsilane to o-quinonediimides: Formal Diels-Alder reaction versus allylation

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Dhanya, R; Vidya, N; Devipriya, S
  • Volume :
  • Year : 2006