Results 11 to 20 of about 281,828 (139)

2‐Aminoindoles and 2‐Iminoindolines as Viable Precursors of Indole‐fused Nitrogenated Polyheterocycles.

open access: yesAdvanced Synthesis & Catalysis
The synthesis of architecturally complex polyheterocyclic structures embedding the indole ring represents a growing field of interest. Carbolines and their partially dehydro derivatives, pyrazinoindoles, indoloindoles, azepinoindoles and other medium ...
Marino Petrini
semanticscholar   +5 more sources

Complex Polyheterocycles and the Stereochemical Reassignment of Pileamartine A via Aza-Heck Triggered Aryl C-H Functionalization Cascades. [PDF]

open access: yesJ Am Chem Soc, 2021
Structurally complex benzo- and spiro-fused N-polyheterocycles can be accessed via intramolecular Pd(0)-catalyzed alkene 1,2-aminoarylation reactions. The method uses N-(pentafluorobenzoyloxy)carbamates as the initiating motif, and this allows aza-Heck ...
Jones BT   +7 more
europepmc   +4 more sources

Ring Reconstruction on a Trichalcogenasumanene Buckybowl: A Facile Approach to Donor–Acceptor‐Type [5‐6‐7] Fused Planar Polyheterocycles

open access: yesAngewandte Chemie - International Edition, 2015
AbstractThe transformation of trichalcogenasumanene buckybowls into donor–acceptor‐type [5‐6‐7] fused polyheterocycles is disclosed. The strategy involves a highly efficient ring‐opening of the flanking benzene upon oxidation at room temperature, and facile ring closure by functional‐group transformation.
Xuexiang Li   +2 more
exaly   +5 more sources

Mo-Catalyzed One-Pot Synthesis of N-Polyheterocycles from Nitroarenes and Glycols with Recycling of the Waste Reduction Byproduct. Substituent-Tuned Photophysical Properties. [PDF]

open access: yesChemistry, 2021
A catalytic domino reduction–imine formation–intramolecular cyclization–oxidation for the general synthesis of a wide variety of biologically relevant N‐polyheterocycles, such as quinoxaline‐ and quinoline‐fused derivatives, and phenanthridines, is ...
Hernández-Ruiz R   +6 more
europepmc   +4 more sources

6-Exo-dig cyclization/dearomatization cascade towards N–O fused spiro polyheterocycles

open access: yesOrganic Chemistry Frontiers, 2023
Herein, we present a metal-free cascade cyclization of alkyne-tethered N-alkoxybenzamides for the construction of structurally novel polyheterocycles.
Erik V Van Der Eycken   +2 more
exaly   +3 more sources

Phenanthridine-Fused Tetracyclic Ring System: Metal-Free Diastereoselective Modular Construction of Highly Constrained Polyheterocycles via Post-Ugi Tandem Modifications.

open access: yesOrganic Letters, 2019
A metal-free diastereo-/regioselective modular synthetic approach for the synthesis of highly constrained tetrahydroquinoline-fused tetracyclic heterocycles from easily available substrates has been developed.
K. Singh   +5 more
semanticscholar   +4 more sources

Aryl Methyl Ketones: Versatile Synthons in the Synthesis of Heterocyclic Compounds [PDF]

open access: yesSynOpen, 2022
The synthesis of aromatic heterocycles has attracted substantial attention due to the abundance of these heterocycles in drug molecules, natural products, and other compounds of biological interest.
Shabber Mohammed   +2 more
doaj   +2 more sources

Metal Coordination-Induced Electronic Tuning in Fused Polyheterocycles: Synthesis and Characterization of Cu, Zn and Fe Complexes of Benzo[a]furo[2,3-c]phenazine, Furo[3′,2′:3,4]naphtho[1,2-d]imidazole and Naphtho[1,2-b]furan-4,5-dione

open access: yesChemistry
We report the synthesis, characterisation and electronic modulation of three novel fused polyheterocyclic ligands—naphtho[1,2-b]furan-4,5-dione (1), furo[3′,2′:3,4]naphtho[1,2-d]imidazole (2), and benzo[a]furo[2,3-c]phenazine (3)—and their Cu(II), Zn(II)
Zoltán Köntös, Máté Varga
doaj   +2 more sources

Rhodium‐Catalyzed Cascade Reactions of Indoles with 4‐Hydroxy‐2‐Alkynoates for the Synthesis of Indole‐Fused Polyheterocycles

open access: yesAdvanced Synthesis & Catalysis, 2020
. Herein, an efficient and regioselective Rh(III)- catalyzed [4+2] annulation/lactonization cascade of indoles with 4-hydroxy-2-alkynoates at room temperature to access the furo[3',4':4,5]pyrimido[1,6-a]indole-1,5(3 H ,4 H )-diones is described.
Xiaowei Wu   +9 more
semanticscholar   +4 more sources

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