Results 1 to 10 of about 119 (101)

Conducting polyheterocycle composites based on porous hosts

open access: yesJournal of Electronic Materials, 1992
Conducting composites based on porous substrates (cotton fiber, non-woven polypropylene mat and porous crosslinked polystyrene) have been prepared by a two step imbibition technique. First, the substrate was imbibed with a solution of monomer (pyrrole or bithiophene) in acetonitrile, followed by partial drying.
J S Park, Ruckenstein E
exaly   +3 more sources

Two Annulated Azaheterocyclic Cores Readily Available from a Single Tetrahydroisoquinolonic Castagnoli–Cushman Precursor

open access: yesMolecules, 2020
A novel approach to indolo[3,2-c]isoquinoline and dibenzo[c,h][1,6]naphthyridine tetracyclic systems was discovered based on switchable reduction of 2-methoxy-3-(2-nitrophenyl)-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylic acid prepared via ...
Elizaveta Karchuganova   +3 more
doaj   +2 more sources

Design and Synthesis of a Conformationally Rigid Mimic of the Dihydropyrimidine Calcium Channel Modulator SQ 32,926

open access: yesMolecules, 2000
A conformationally rigid polyheterocycle (3) which mimics the putative receptorbound conformation of dihydropyridine-type calcium channel modulators is prepared in a seven-step reaction sequence based on a Biginelli-type cyclocondensation reaction.
Birgit Jauk   +2 more
doaj   +2 more sources

4,5,6,7-Tetrahydroindol-4-Ones as a Valuable Starting Point for the Synthesis of Polyheterocyclic Structures

open access: yesMolecules, 2021
This review focuses on the synthesis of polyheterocyclic structures with a variety of medicinal and optoelectronic applications, starting from readily available 4,5,6,7-tetrahydroindol-4-one analogs. First, routes toward the 4,5,6,7-tetrahydroindol-4-one
Tomáš Horsten   +2 more
exaly   +3 more sources

Pd(II)-Catalyzed [4 + 2] Heterocyclization Sequence for Polyheterocycle Generation [PDF]

open access: yesOrganic Letters, 2018
A new Pd(II)-catalyzed cascade sequence for the formation of polyheterocycles, from simple starting materials, is reported. The sequence is applicable to both indole and pyrrole substrates, and a range of substituents are tolerated.
Kevin I Booker-Milburn
exaly   +2 more sources

A Palladium(II)‐Catalyzed CH Activation Cascade Sequence for Polyheterocycle Formation

open access: yesAngewandte Chemie, 2015
Polyheterocycles are found in many natural products and are useful moieties in functional materials and drug design. As part of a program towards the synthesis of Stemona alkaloids, a novel palladium(II)-catalyzed C-H activation strategy for the ...
Kevin I Booker-Milburn
exaly   +4 more sources

Fused-Ring Oxazolopyrrolopyridopyrimidine Systems with Gram-Negative Activity

open access: yesAntibiotics, 2017
Fused polyheterocyclic derivatives are available by annulation of a tetramate scaffold, and been shown to have antibacterial activity against a Gram-negative, but not a Gram-positive, bacterial strain.
Yiyuan Chen   +2 more
exaly   +3 more sources

(8R,10aS)-Methyl 2,4-diamino-8-(tert-butyl)-6-oxo-6,8,10,10a-tetrahydrooxazolo[3′′,4′′:1′,5′]-pyrrolo[3′,4′:5,6]pyrido[2,3-d]pyrimidine-10a-carboxylate

open access: yesMolBank, 2015
A fused polyheterocyclic derivative is available by annulation of a tetramate scaffold, and has been shown to have some Gram-negative, but not Gram-positive, antibacterial activity.
Mark G Moloney
exaly   +3 more sources

Silver‐Catalyzed Carbon‐Phosphorus Functionalization for Polyheterocycle Formation

open access: yesAdvanced Synthesis and Catalysis, 2017
Jianming Liu   +2 more
exaly   +2 more sources

Copper-Catalyzed Modular Assembly of Polyheterocycles [PDF]

open access: yesThe Journal of Organic Chemistry, 2020
Easy operation, readily accessible starting materials, and short syntheses of the privileged scaffold indeno[1,2-c]isoquinolinone were achieved by an multicomponent reaction (MCR)-based protocol via an ammonia-Ugi-four component reaction (4CR)/copper-catalyzed annulation sequence.
Qian Wang   +5 more
openaire   +3 more sources

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