Results 11 to 20 of about 1,317 (206)

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

Molybdenum‐Catalyzed One‐Pot Multi‐Step Synthesis of N‐Polyheterocycles from Nitroarenes and Glycols [PDF]

open access: yesEuropean Journal of Organic Chemistry, Volume 27, Issue 18, May 13, 2024.
We report the efficient, sustainable one-pot synthesis of a wide variety of N-polyheterocycles, such as imidazo-quinolines and quinoxalines, and furoquinolines, from easily available nitroaromatics and glycols via a molybdenum catalytic domino reduction ...
Cases, Nuria   +6 more
core   +3 more sources

Highly Stereoselective Ugi/Pictet-Spengler Sequence. [PDF]

open access: yesJ Org Chem, 2022
Discovering novel synthetic routes for rigid nitrogen-containing polyheterocycles using sustainable, atom-economical, and efficient (= short) synthetic pathways is of high interest in organic chemistry. Here, we describe an operationally simple and short
Zhang B, Kurpiewska K, Dömling A.
europepmc   +4 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

Cp∗Rh/Ag catalyzed C–H activation/cyclization sequences of NH-sulfoximines to fused aza-polyheterocycles under gentle conditions

open access: yesGreen Synthesis and Catalysis, 2023
Disclosed herein is a novel Rh/Ag co-catalyzed SNH directed C–H activation and C–H/N–H bond functionalization protocol of free NH-sulfoximines with hypervalent iodonium ylides.
Jiapian Huang   +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

Rhodacyclopentanones as Linchpins for the Atom Economical Assembly of Diverse Polyheterocycles [PDF]

open access: yesJournal of the American Chemical Society, 2020
We outline a conceptual blueprint that provides direct and atom economical access to a wide range of complex polyheterocycles. Our method capitalizes on the ambiphilic reactivity of rhodacyclopentanones that arise upon exposure of cyclopropanes to Rh(I ...
Bertrand, Sophie M.   +4 more
core   +3 more sources

Intramolecular Povarov Reactions for the Synthesis of Chromenopyridine Fused 2-Pyridone Polyheterocycles Binding to α-Synuclein and Amyloid-β Fibrils. [PDF]

open access: yesJ Org Chem, 2020
A BF3·OEt2 catalyzed intramolecular Povarov reaction was used to synthesize 15 chromenopyridine fused thiazolino-2-pyridone peptidomimetics. The reaction works with several O-alkylated salicylaldehydes and amino functionalized thiazolino-2-pyridones, to ...
Adolfsson DE   +10 more
europepmc   +2 more sources

An easy access to furan fused polyheterocyclic systems [PDF]

open access: yesMolecules, 2022
Nitrostilbenes characterized by two different or differently substituted aryl moieties can be obtained from the initial ring-opening of 3-nitrobenzo[b]thiophene with amines.
Alice Benzi   +6 more
core   +5 more sources

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