9 research outputs found
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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline 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 indolylcyclopenta[<i>b</i>]quinoline derivatives
Techniques and methods of assessing projects including inflation
Навчальний посібник виготовлено відповідно до програми з нормативної навчальної дисципліни "Фінансовий менеджмент", яку включено до навчального плану підгтовки освітньо-кваліфікаційного рівня "спеціаліст" і "магістр" спеціальностей. У ньому викладено сутність і завдання фінансового менеджменту, підходи до управління активами, капіталом, інвестиціями, фінансовими ризиками підприємства, основи управління вартістю бізнесу.The book is made in accordance with the program of regulatory discipline "Financial Management", which is included in the educational program for qualification of "expert" and "master" specialties. It outlines the nature and objectives of financial management, approaches to asset management, capital investment, financial risk companies, foundations of business value
Synthesis of Isocoumarin Derivatives via the Copper-Catalyzed Tandem Sequential Cyclization of 2- Halo-<i>N</i>-phenyl Benzamides and Acyclic 1,3-Diketones
A facile and rapid synthesis of isocoumarin derivatives
using a
copper-catalyzed tandem C–C/C–O coupling strategy from
readily available substrates is described. The reactions of a wide
range of 2-iodo-<i>N</i>-phenyl benzamides and acyclic diketones
as starting materials were investigated
Synthesis of Isocoumarin Derivatives via the Copper-Catalyzed Tandem Sequential Cyclization of 2- Halo-<i>N</i>-phenyl Benzamides and Acyclic 1,3-Diketones
A facile and rapid synthesis of isocoumarin derivatives
using a
copper-catalyzed tandem C–C/C–O coupling strategy from
readily available substrates is described. The reactions of a wide
range of 2-iodo-<i>N</i>-phenyl benzamides and acyclic diketones
as starting materials were investigated
Synthesis of Isocoumarin Derivatives via the Copper-Catalyzed Tandem Sequential Cyclization of 2- Halo-<i>N</i>-phenyl Benzamides and Acyclic 1,3-Diketones
A facile and rapid synthesis of isocoumarin derivatives
using a
copper-catalyzed tandem C–C/C–O coupling strategy from
readily available substrates is described. The reactions of a wide
range of 2-iodo-<i>N</i>-phenyl benzamides and acyclic diketones
as starting materials were investigated