Results 1 to 10 of about 888 (170)

Complexity-Building ESIPT-Assisted Synthesis of Fused Polyheterocyclic Sulfonamides [PDF]

open access: yesMolecules, 2023
Excited State Intramolecular Proton Transfer (ESIPT), originally discovered and explored in depth in a number of extensive photophysical studies, is more recently rediscovered as a powerful synthetic tool, offering rapid access to complex ...
Srinivas Beduru, Andrei G. Kutateladze
doaj   +4 more sources

Palladium‐Catalyzed Dual Csp2─Csp3 Bond Formation: A Versatile Platform for the Synthesis of Benzo‐Fused Heterocycles [PDF]

open access: yesAdvanced Science
Transition‐metal‐catalyzed transformations offer a powerful approach to rapidly synthesize complex benzo‐fused heterocycles, crucial for drug and material development.
Jiahui Huang   +9 more
doaj   +3 more sources

Synthesis of New Polyheterocyclic Pyrrolo[3,4-b]pyridin-5-ones via an Ugi-Zhu/Cascade/Click Strategy [PDF]

open access: yesMolecules, 2023
A diversity-oriented synthesis (DOS) of two new polyheterocyclic compounds was performed via an Ugi-Zhu/cascade (N-acylation/aza Diels-Alder cycloaddition/decarboxylation/dehydration)/click strategy, both step-by-step to optimize all involved ...
Roberto E. Blanco-Carapia   +4 more
doaj   +2 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

One-Pot Sequence of Staudinger/aza-Wittig/Castagnoli–Cushman Reactions Provides Facile Access to Novel Natural-like Polycyclic Ring Systems [PDF]

open access: yesMolecules, 2022
Realization of the one-pot Staudinger/aza-Wittig/Castagnoli–Cushman reaction sequence for a series of azido aldehydes and homophthalic anhydrides is described. The reaction proceeded at room temperature and delivered novel polyheterocycles related to the
Rodion Lebedev   +4 more
doaj   +2 more sources

Free-radical cyclization approach to polyheterocycles containing pyrrole and pyridine rings [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2021
A wide range of derivatives with new pyrido[2,1-a]pyrrolo[3,4-c]isoquinoline skeleton was synthesized by free-radical intramolecular cyclization of o-bromophenyl-substituted pyrrolylpyridinium salts using the (TMS)3SiH/AIBN system.
Ivan P. Mosiagin   +5 more
doaj   +2 more sources

Recent Developments in Azomethine Ylide-Initiated Double Cycloadditions [PDF]

open access: yesMolecules
Azomethine ylides (AMYs) have a nitrogen–carbon double bond and an electron lone pair on the nitrogen atom. They are essential 1,3-dipoles for [3+2] cycloadditions in the synthesis of pyrrolidine-containing heterocycles.
Tieli Zhou   +4 more
doaj   +2 more sources

Synthetic routes to benzimidazole-based fused polyheterocycles [PDF]

open access: yesARKIVOC, 2010
The review article represents a survey covering the synthetic strategies leading to benzimidazole- based fused polyheterocyclic systems utilizing simple reactive benzimidazole synthons since 1980. The polyheterocyclic systems are classified based on the number of rings; tetra-, penta-, hexa- and hepta-fused ring systems.
Kamal M. Dawood, Bakr F. Abdel-Wahab
doaj   +2 more sources

Enantioselective aza-electrophilic dearomatization of naphthalene derivatives [PDF]

open access: yesNature Communications
The catalytic asymmetric dearomatization of naphthalenes is a pivotal strategy for generating enantioenriched three-dimensional aliphatic polycycles from flat aromatic precursors.
Jun Liu   +5 more
doaj   +2 more sources

Diverse Synthesis of Fused Polyheterocyclic Compounds via [3 + 2] Cycloaddition of In Situ-Generated Heteroaromatic N-Ylides and Electron-Deficient Olefins [PDF]

open access: yesMolecules, 2023
[3 + 2] Cycloaddition reactions of heteroaromatic N-ylides with electron-deficient olefins have been developed. The heteroaromatic N-ylides, in situ generated from N-phenacylbenzothiazolium bromides, can smoothly react with maleimides under very mild ...
Zhen-Hua Wang   +7 more
doaj   +2 more sources

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