Boron trifluoride-etherate induced rearrangement of bicyclo[2.2.2]octenediones: An efficient synthesis of bicyclo[3.2.1]octenediones

Boron trifluoride-etherate induced rearrangement of bicyclo[2.2.2]octenediones: An efficient synthesis of bicyclo[3.2.1]octenediones

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Maliakal, D; Treesa, PM; Anilkumar, G; Vairamani, M; Prabhakar, S; Rath, NP
  • Volume :
  • Year : 2000
Cerium(IV) ammonium nitrate induced dimerization of methoxystyrenes

Cerium(IV) ammonium nitrate induced dimerization of methoxystyrenes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Sheeba, V; Panicker, SB; George, TG; Rajan, R; Balagopal, L; Vairamani, M; Prabhakar, S
  • Volume :
  • Year : 2000
Cerium(IV) ammonium nitrate mediated addition of thiocyanate and azide to styrenes: Expeditious routes to phenacyl thiocyanates and phenacyl azides

Cerium(IV) ammonium nitrate mediated addition of thiocyanate and azide to styrenes: Expeditious routes to phenacyl thiocyanates and phenacyl azides

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Nair, LG; George, TG; Augustine, A
  • Volume :
  • Year : 2000
Protein folding: The synthesis and conformational studies on cystinyl-cystinyl-cystine [-CSSCCSSCCSSC-] a novel cross linking motif

Protein folding: The synthesis and conformational studies on cystinyl-cystinyl-cystine [-CSSCCSSCCSSC-] a novel cross linking motif

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Ranganathan, S; Tamilarasu, N; Roy, R
  • Volume :
  • Year : 1996
Diels-Alder reactions of a 6-arenyl fulvene with dienes and dienophiles and related chemistry

Diels-Alder reactions of a 6-arenyl fulvene with dienes and dienophiles and related chemistry

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Anilkumar, G; Radhakrishnan, KV; Sheela, KC; Rath, NP
  • Volume :
  • Year : 1997
2-aza-3-oxabicyclo[2.2.1]heptene hydrochloride: An exceptionally versatile synthon for carbocyclic sugars and nucleosides

2-aza-3-oxabicyclo[2.2.1]heptene hydrochloride: An exceptionally versatile synthon for carbocyclic sugars and nucleosides

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Ranganathan, S; George, KS
  • Volume :
  • Year : 1997
Photoelectron transfer induced decarboxylation of substituted carboxylic acids across a liquid/liquid interface

Photoelectron transfer induced decarboxylation of substituted carboxylic acids across a liquid/liquid interface

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Rajesh, CS; Thanulingam, TL; Das, S
  • Volume :
  • Year : 1997
Photolytic double decarbonylation route to highly substituted indenes and benzene derivatives

Photolytic double decarbonylation route to highly substituted indenes and benzene derivatives

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Thomas, A; Anilkumar, G; Nair, V
  • Volume :
  • Year : 1996
Cycloaddition reactions of 3-ethoxycarbonyl-2H-cyclohepta[b]furan-2-one with 6,6-dialkyl, cycloalkyl and diaryl pentafulvenes

Cycloaddition reactions of 3-ethoxycarbonyl-2H-cyclohepta[b]furan-2-one with 6,6-dialkyl, cycloalkyl and diaryl pentafulvenes

  • --- Research Area : Chemical Sciences & Technology Division (CSTD)
  • Author : Nair, V; Anilkumar, G; Radhakrishnan, KV; Nandakumar, MV; Kumar, S
  • Volume :
  • Year : 1997