40 research outputs found
ChemInform Abstract: Molecular Iodine-Mediated Reaction of 2-(2-Phenylethynyl)-Morita-Baylis-Hillman Adducts: An Easy Route to Naphthyl Ketones and Iodo-Substituted Isochromenes.
ChemInform Abstract: Palladium(II) Chloride-Catalyzed Aerobic Oxidative Intermolecular Cycloaddition Reaction of 2-Alkynylbenzaldehydes and Electron-Deficient Terminal Alkenes: An Efficient Synthesis of Naphthyl Ketones.
Synthesis of Indolylquinolines, Indolylacridines, and Indolylcyclopenta[<i>b</i>]quinolines from the Baylis–Hillman Adducts: An in Situ [1,3]-Sigmatropic Rearrangement of an Indole Nucleus To Access Indolylacridines and Indolylcyclopenta[<i>b</i>]quinolines
A simple and easy route to the synthesis of a variety
of structurally
diverse indolylquinolines, indolylacridines, and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives via the reductive cyclization of
C-alkylated indole derivatives, derived from acyclic as well as cyclic
Baylis–Hillman adducts with indoles, is described. An unusual
in situ [1,3]-sigmatropic rearrangement of the indole nucleus was
observed during the reductive cyclicization of α-regioselective
B–H adducts containing indoles to produce indolylacridines
and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives
Synthesis of Indolylquinolines, Indolylacridines, and Indolylcyclopenta[<i>b</i>]quinolines from the Baylis–Hillman Adducts: An in Situ [1,3]-Sigmatropic Rearrangement of an Indole Nucleus To Access Indolylacridines and Indolylcyclopenta[<i>b</i>]quinolines
A simple and easy route to the synthesis of a variety
of structurally
diverse indolylquinolines, indolylacridines, and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives via the reductive cyclization of
C-alkylated indole derivatives, derived from acyclic as well as cyclic
Baylis–Hillman adducts with indoles, is described. An unusual
in situ [1,3]-sigmatropic rearrangement of the indole nucleus was
observed during the reductive cyclicization of α-regioselective
B–H adducts containing indoles to produce indolylacridines
and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives
Synthesis of Indolylquinolines, Indolylacridines, and Indolylcyclopenta[<i>b</i>]quinolines from the Baylis–Hillman Adducts: An in Situ [1,3]-Sigmatropic Rearrangement of an Indole Nucleus To Access Indolylacridines and Indolylcyclopenta[<i>b</i>]quinolines
A simple and easy route to the synthesis of a variety
of structurally
diverse indolylquinolines, indolylacridines, and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives via the reductive cyclization of
C-alkylated indole derivatives, derived from acyclic as well as cyclic
Baylis–Hillman adducts with indoles, is described. An unusual
in situ [1,3]-sigmatropic rearrangement of the indole nucleus was
observed during the reductive cyclicization of α-regioselective
B–H adducts containing indoles to produce indolylacridines
and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives
Synthesis of Indolylquinolines, Indolylacridines, and Indolylcyclopenta[<i>b</i>]quinolines from the Baylis–Hillman Adducts: An in Situ [1,3]-Sigmatropic Rearrangement of an Indole Nucleus To Access Indolylacridines and Indolylcyclopenta[<i>b</i>]quinolines
A simple and easy route to the synthesis of a variety
of structurally
diverse indolylquinolines, indolylacridines, and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives via the reductive cyclization of
C-alkylated indole derivatives, derived from acyclic as well as cyclic
Baylis–Hillman adducts with indoles, is described. An unusual
in situ [1,3]-sigmatropic rearrangement of the indole nucleus was
observed during the reductive cyclicization of α-regioselective
B–H adducts containing indoles to produce indolylacridines
and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives
Synthesis of Indolylquinolines, Indolylacridines, and Indolylcyclopenta[<i>b</i>]quinolines from the Baylis–Hillman Adducts: An in Situ [1,3]-Sigmatropic Rearrangement of an Indole Nucleus To Access Indolylacridines and Indolylcyclopenta[<i>b</i>]quinolines
A simple and easy route to the synthesis of a variety
of structurally
diverse indolylquinolines, indolylacridines, and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives via the reductive cyclization of
C-alkylated indole derivatives, derived from acyclic as well as cyclic
Baylis–Hillman adducts with indoles, is described. An unusual
in situ [1,3]-sigmatropic rearrangement of the indole nucleus was
observed during the reductive cyclicization of α-regioselective
B–H adducts containing indoles to produce indolylacridines
and indolylcyclopentaÂ[<i>b</i>]Âquinoline derivatives