The Experts below are selected from a list of 294 Experts worldwide ranked by ideXlab platform

C. V. Asokan - One of the best experts on this subject based on the ideXlab platform.

Marcus Bollyn - One of the best experts on this subject based on the ideXlab platform.

  • thermal hazards of the Vilsmeier Haack Reaction on n n dimethylaniline
    Organic Process Research & Development, 2005
    Co-Authors: Marcus Bollyn
    Abstract:

    From literature data and a preliminary calorimetric study it is clear that the VilsmeierHaack Reaction poses specific thermal hazards as both the VilsmeierHaack intermediate (1) in N,N-dimethylformamide (2) and the Reaction mixture with N,N-dimethylaniline (3) are thermally unstable and can generate high and fast temperature and pressures rises when heated. Therefore alternatives were investigated for their thermal hazards. The stability of Vilsmeier intermediates generated from a series of other formamides was investigated. In principle the Vilsmeier intermediate could be generated and converted in situ, thus avoiding large amounts of an unstable intermediate in the process vessel and yielding the same Reaction mixture. This concept could also be applied to the other formamides studied, and this option was also included in the investigation.

  • Thermal Hazards of the VilsmeierHaack Reaction on N,N-Dimethylaniline
    Organic Process Research & Development, 2005
    Co-Authors: Marcus Bollyn
    Abstract:

    From literature data and a preliminary calorimetric study it is clear that the VilsmeierHaack Reaction poses specific thermal hazards as both the VilsmeierHaack intermediate (1) in N,N-dimethylformamide (2) and the Reaction mixture with N,N-dimethylaniline (3) are thermally unstable and can generate high and fast temperature and pressures rises when heated. Therefore alternatives were investigated for their thermal hazards. The stability of Vilsmeier intermediates generated from a series of other formamides was investigated. In principle the Vilsmeier intermediate could be generated and converted in situ, thus avoiding large amounts of an unstable intermediate in the process vessel and yielding the same Reaction mixture. This concept could also be applied to the other formamides studied, and this option was also included in the investigation.

Mmakwena M. Mmonwa - One of the best experts on this subject based on the ideXlab platform.

  • VilsmeierHaack Reaction of 7-acetyl-2-arylindoles: a convenient method for the synthesis of 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes
    Organic & biomolecular chemistry, 2019
    Co-Authors: Malose J. Mphahlele, Mmakwena M. Mmonwa
    Abstract:

    A simple and efficient method for the one-pot synthesis of novel 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes via the VilsmeierHaack Reaction of the corresponding 7-acetyl-2-arylindoles has been developed. The mechanism of this Reaction is envisaged to involve initial C-3 formylation and subsequent diformylation at the acetyl group with the excess VilsmeierHaack reagent followed by heteroannulation of the six-membered ring with concomitant extrusion of dimethylamine to afford the 1,2,5,8-tetrasubstituted pyrroloquinolinones. The highlight of this method is the construction of carbon–carbon and carbon–nitrogen bonds in a single-pot operation to afford polycarbo-substituted pyrroloquinolinones.

  • Vilsmeier Haack Reaction of 7 acetyl 2 arylindoles a convenient method for the synthesis of 6 oxo 6h pyrrolo 3 2 1 ij quinoline 1 5 dicarbaldehydes
    Organic and Biomolecular Chemistry, 2019
    Co-Authors: Malose J. Mphahlele, Mmakwena M. Mmonwa
    Abstract:

    A simple and efficient method for the one-pot synthesis of novel 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes via the VilsmeierHaack Reaction of the corresponding 7-acetyl-2-arylindoles has been developed. The mechanism of this Reaction is envisaged to involve initial C-3 formylation and subsequent diformylation at the acetyl group with the excess VilsmeierHaack reagent followed by heteroannulation of the six-membered ring with concomitant extrusion of dimethylamine to afford the 1,2,5,8-tetrasubstituted pyrroloquinolinones. The highlight of this method is the construction of carbon–carbon and carbon–nitrogen bonds in a single-pot operation to afford polycarbo-substituted pyrroloquinolinones.

Palathurai Subramaniam Mohan - One of the best experts on this subject based on the ideXlab platform.

Malose J. Mphahlele - One of the best experts on this subject based on the ideXlab platform.

  • VilsmeierHaack Reaction of 7-acetyl-2-arylindoles: a convenient method for the synthesis of 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes
    Organic & biomolecular chemistry, 2019
    Co-Authors: Malose J. Mphahlele, Mmakwena M. Mmonwa
    Abstract:

    A simple and efficient method for the one-pot synthesis of novel 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes via the VilsmeierHaack Reaction of the corresponding 7-acetyl-2-arylindoles has been developed. The mechanism of this Reaction is envisaged to involve initial C-3 formylation and subsequent diformylation at the acetyl group with the excess VilsmeierHaack reagent followed by heteroannulation of the six-membered ring with concomitant extrusion of dimethylamine to afford the 1,2,5,8-tetrasubstituted pyrroloquinolinones. The highlight of this method is the construction of carbon–carbon and carbon–nitrogen bonds in a single-pot operation to afford polycarbo-substituted pyrroloquinolinones.

  • Vilsmeier Haack Reaction of 7 acetyl 2 arylindoles a convenient method for the synthesis of 6 oxo 6h pyrrolo 3 2 1 ij quinoline 1 5 dicarbaldehydes
    Organic and Biomolecular Chemistry, 2019
    Co-Authors: Malose J. Mphahlele, Mmakwena M. Mmonwa
    Abstract:

    A simple and efficient method for the one-pot synthesis of novel 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes via the VilsmeierHaack Reaction of the corresponding 7-acetyl-2-arylindoles has been developed. The mechanism of this Reaction is envisaged to involve initial C-3 formylation and subsequent diformylation at the acetyl group with the excess VilsmeierHaack reagent followed by heteroannulation of the six-membered ring with concomitant extrusion of dimethylamine to afford the 1,2,5,8-tetrasubstituted pyrroloquinolinones. The highlight of this method is the construction of carbon–carbon and carbon–nitrogen bonds in a single-pot operation to afford polycarbo-substituted pyrroloquinolinones.