Transition-metal mediated carbon–sulfur bond activation and transformations: an update
J Lou, Q Wang, P Wu, H Wang, YG Zhou… - Chemical Society …, 2020 - pubs.rsc.org
Carbon–sulfur bond cross-coupling has become more and more attractive as an alternative
protocol to establish carbon–carbon and carbon–heteroatom bonds. Diverse …
protocol to establish carbon–carbon and carbon–heteroatom bonds. Diverse …
Advances in palladium‐catalyzed cascade cyclizations
The past decades in organic chemistry have witnessed significant improvements in synthetic
efficiency as a result of considerable progress in cascade reactions, tandem reactions, and …
efficiency as a result of considerable progress in cascade reactions, tandem reactions, and …
Palladium-Catalyzed Approach to the Synthesis of S-heterocycles
N Kaur - Catalysis Reviews, 2015 - Taylor & Francis
Heterocyclic compounds containing sulfur atom is an important division of compounds which
play important role in new drug development. The S-heterocycles synthesis and their …
play important role in new drug development. The S-heterocycles synthesis and their …
Na2S·9H2O Enabled Defluorodisulfuration and Hydrodefluorination of Perfluorobutyl Tetralones: Synthesis of Trifluoromethyl 1,2-Dithioles
ZL Yu, MH Feng, PY Zhang, H Xu, D Ge, M Ma… - Organic …, 2023 - ACS Publications
An unprecedented defluorocyclization of perfluorobutyl tetralones with Na2S· 9H2O was
developed for the synthesis of trifluoromethyl 1, 2-dithioles, which provided chemists novel …
developed for the synthesis of trifluoromethyl 1, 2-dithioles, which provided chemists novel …
Access to Fully Substituted Thiazoles and 2,3-Dihydrothiazoles via Copper-Catalyzed [4 + 1] Heterocyclization of α-(N-Hydroxy/aryl)imino-β-oxodithioesters with α …
An efficient chemoselective practical route to fully substituted thiazoles and 2, 3-
dihydrothiazoles has been devised by [4+ 1] heterocyclization of α-(N-hydroxy/aryl) imino-β …
dihydrothiazoles has been devised by [4+ 1] heterocyclization of α-(N-hydroxy/aryl) imino-β …
Metal-free one-pot four-component cascade annulation in ionic liquids at room temperature: convergent access to Thiazoloquinolinone derivatives
A Singh, A Srivastava, MS Singh - The Journal of Organic …, 2018 - ACS Publications
An efficient, eco-friendly, and highly convergent one-pot route to privileged
thiazoloquinolinone derivatives has been developed via four-component cascade coupling …
thiazoloquinolinone derivatives has been developed via four-component cascade coupling …
Copper-catalyzed one-pot cross-dehydrogenative thienannulation: Chemoselective access to naphtho [2, 1-b] thiophene-4, 5-diones and subsequent transformation …
A facile, cost-effective, and highly efficient copper-catalyzed, TEMPO-mediated
straightforward synthesis of 2, 3-disubstituted naphtho [2, 1-b] thiophene-4, 5-diones has …
straightforward synthesis of 2, 3-disubstituted naphtho [2, 1-b] thiophene-4, 5-diones has …
Regioselective dehydrative intramolecular heteroannulation of β-allyl-β-hydroxy dithioesters: facile and straightforward entry to 2H-thiopyrans
Abstract β-Allyl-β-hydroxy dithioesters have been employed in the synthesis of hitherto
unreported and synthetically demanding 2 H-thiopyrans via regioselective intramolecular …
unreported and synthetically demanding 2 H-thiopyrans via regioselective intramolecular …
A Study of [3+ 2] Cycloaddition Reaction of Hydrazonoyl Chloride and β‐Oxodithioester Under Lewis Acid Catalysis: Stereoselective Synthesis of (Z)‐1, 3, 4 …
RK Chellu, S Kurva, AK Soda… - Asian Journal of …, 2021 - Wiley Online Library
Hydrazonoyl chlorides underwent unprecedented stereoselective [3+ 2] cycloaddition
reaction with β‐oxodithioesters and β‐oxothioamides under Lewis acid catalysis producing …
reaction with β‐oxodithioesters and β‐oxothioamides under Lewis acid catalysis producing …
Regioselective Synthesis of Dihydrothiophene and Thiopyran Frameworks via Catalyst-Controlled Intramolecular Cγ/Cδ–S Fusion of α-Allyl-β′-oxodithioesters
A highly efficient and atom-economic dual reaction manifold has been developed to
synthesize 4 H-thiopyran and 4, 5-dihydrothiophene frameworks via regioselective …
synthesize 4 H-thiopyran and 4, 5-dihydrothiophene frameworks via regioselective …