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A facile three-component reaction involving [4+1] cycloaddition leading to furan annulated heterocycles

A facile three-component reaction involving [4+1] cycloaddition leading to furan annulated heterocycles

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Menon, RS; Vinod, AU; Viji, S
  • Volume :
  • Year : 2002
An efficient one-pot synthesis of vinyl sulphones via CAN mediated reaction of aryl sulphinates and alkenes

An efficient one-pot synthesis of vinyl sulphones via CAN mediated reaction of aryl sulphinates and alkenes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Augustine, A; George, TG; Nair, LG
  • Volume :
  • Year : 2001
The reaction of cyclohexyl isocyanide and dimethyl acetylenedicarboxylate with o- and p-quinones: a novel synthesis of iminolactones

The reaction of cyclohexyl isocyanide and dimethyl acetylenedicarboxylate with o- and p-quinones: a novel synthesis of iminolactones

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Vinod, AU; Nair, JS; Sreekanth, AR; Rath, NP
  • Volume :
  • Year : 2000
Formal dipolar cycloaddition of allylsilanes to o-quinonoid compounds: a convenient route to benzofused and spirofused heterocycles

Formal dipolar cycloaddition of allylsilanes to o-quinonoid compounds: a convenient route to benzofused and spirofused heterocycles

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Rajesh, C; Dhanya, R; Rath, NP
  • Volume :
  • Year : 2002
Hetero Diels-Alder trapping of 3-methylene-1,2,4-[3H]naphthalenetrione: an efficient protocol for the synthesis of alpha- and beta-lapachone derivatives

Hetero Diels-Alder trapping of 3-methylene-1,2,4-[3H]naphthalenetrione: an efficient protocol for the synthesis of alpha- and beta-lapachone derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Treesa, PM
  • Volume :
  • Year : 2001
A novel CAN-mediated oxidative rearrangement of monoterpenes

A novel CAN-mediated oxidative rearrangement of monoterpenes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Rajan, R; Balagopal, L; Thomas, S; Narasimlu, K
  • Volume :
  • Year : 2002
Cerium(IV) mediated oxygenation of dialkyl malonates: A novel synthesis of tartronic acid derivatives.

Cerium(IV) mediated oxygenation of dialkyl malonates: A novel synthesis of tartronic acid derivatives.

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Nair, LG; Mathew, J
  • Volume :
  • Year : 1998
Cycloaddition reactions of carbonyl ylides to [60] fullerene: Synthesis of novel C60 derivatives

Cycloaddition reactions of carbonyl ylides to [60] fullerene: Synthesis of novel C60 derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair V., Sethumadhavan D., Sheela K.C., Eigendorf G.K.
  • Volume :
  • Year : 1999
Novel 1,3-dipolar cycloaddition reaction of carbonyl ylide with o-quinones

Novel 1,3-dipolar cycloaddition reaction of carbonyl ylide with o-quinones

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Sheela, KC; Radhakrishnan, KV; Rath, NP
  • Volume :
  • Year : 1998
Hetero Diels-Alder reactions of o-thioquinones with pentafulvenes: efficient synthesis of novel benzoxathiins

Hetero Diels-Alder reactions of o-thioquinones with pentafulvenes: efficient synthesis of novel benzoxathiins

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Mathew, B
  • Volume :
  • Year : 2000