Research graph
References from K2CO3-Catalyzed Rapid Conversion of N -Sulfonylhydrazones to Sulfinates. Local targets link to admitted publications; unresolved targets remain external evidence.
Recent developments in the synthesis and utilization of chiral sulfoxides
10.1021/cr990372u · 2003 · External reference
Synthesis and Applications of tert-butanesulfinamide
10.1021/cr900382t · 2010 · External reference
Bismuth(III) bromide-catalysed substitution of benzyl alcohols with arylsulfonylmethyl isocyanides: an unexpected access to sulfinates
10.1002/adsc.201401173 · 2015 · External reference
Highly sensitive bioluminescent probe for thiol detection in living cells
10.1002/asia.201701774 · 2018 · External reference
The two faces of sulfinates: illustrating umpolung reactivity
10.1021/acs.jchemed.6b00102 · 2016 · External reference
Methyl sulfinates as electrophiles in Friedel–Crafts reactions. Synthesis of aryl sulfoxides
10.1021/jo2006335 · 2011 · External reference
Sulfinate derivatives: dual and versatile partners in organic synthesis
10.1039/c4ob01727g · 2014 · External reference
Alkyl sulfinates: formal nucleophiles for synthesizing TosMIC analogs
10.1002/ejoc.201403615 · 2015 · External reference
Asymmetric synthesis of sulfinamides using (−)-quinine as chiral auxiliary
10.1021/jo201825b · 2012 · External reference
Recent developments in the synthesis and utilization of chiral sulfoxides
10.1021/cr990372u · 2003 · External reference
Electrochemical synthesis of sulfinic esters via aerobic oxidative esterification of thiophenols with alcohols
10.1055/s-0040-1707966 · 2020 · External reference
Electrochemical synthesis of sulfinic esters from alcohols and thiophenols
10.1016/j.tetlet.2020.151631 · 2020 · External reference
Metal- and oxidant-free electrochemical synthesis of sulfinic esters from thiols and alcohols
10.1039/c9gc02125f · 2019 · External reference
A sustainable oxidative esterification of thiols with alcohols by a cobalt nanocatalyst supported on doped carbon
10.1039/c8gc00441b · 2018 · External reference
Copper-catalyzed aerobic formation of unstable sulfinyl radicals for the synthesis of sulfinates and thiosulfonates
10.1002/adsc.201500785 · 2016 · External reference
TBHP/TBAI-mediated oxidation of thiophenols for the synthesis of tert-butyl arylsulfinates
10.1016/j.tetlet.2018.08.048 · 2018 · External reference
Copper-catalyzed aerobic oxidative reaction of sulfonyl hydrazides with alcohols: an easy access to sulfinates
10.1002/asia.201501262 · 2016 · External reference
tert-Butyl sulfoxide as a starting point for the synthesis of sulfinyl containing compounds
10.1021/acs.orglett.5b02743 · 2015 · External reference
Sulfination of alcohols with sodium sulfinates promoted by BF3.OEt2: an unexpected access
10.1039/c5gc02846a · 2016 · External reference
Sodium arenesulfinates-involved sulfinate synthesis revisited: improved synthesis and revised reaction mechanism
10.1002/ejoc.201900097 · 2019 · External reference
Non-expensive, open-flask and selective catalytic systems for the synthesis of sulfinate esters and thiosulfonates
10.1016/j.tetlet.2017.02.025 · 2017 · External reference
Sulfination of alcohols with p-toluenesulfonylmethyl isocyanide under metal-free conditions: a Mitsunobu approach
10.1002/adsc.201600997 · 2016 · External reference
Tosylhydrazones: new uses for classic reagents in palladium-catalyzed cross-coupling and metal-free reactions
10.1002/anie.201007961 · 2011 · External reference
N-Tosylhydrazones: versatile reagents for metal-catalyzed and metal-free cross-coupling reactions
10.1039/c1cs15127d · 2012 · External reference
Diazo compounds and N-tosylhydrazones: novel cross-coupling partners in transition-metal-catalyzed reactions
10.1021/ar300101k · 2013 · External reference
Catalytic cascade reactions involving metal carbene migratory insertion
10.1021/cs4006666 · 2013 · External reference
Copper-catalyzed direct cross-coupling of compounds containing activated C–H/heteroatom–H bonds with N-tosylhydrazones
10.1002/ejoc.201600074 · 2016 · External reference
C–H bond functionalization based on metal carbene migratory insertion
10.1039/c5cc00497g · 2015 · External reference
Transition-metal-catalyzed cross-couplings through carbene migratory insertion
10.1021/acs.chemrev.7b00382 · 2017 · External reference
N-Tosylhydrazones: versatile synthons in the construction of cyclic compounds
10.1039/c6cs00737f · 2017 · External reference
An update of N-tosylhydrazones: versatile reagents for metal-catalyzed and metal-free coupling reactions
10.1055/s-0036-1591993 · 2018 · External reference
Luxury of N-tosylhydrazones in transition-metal-free transformations
10.1002/adsc.201801031 · 2019 · External reference
Domino synthesis of benzo-fused β,γ-unsaturated ketones from alkenylboronic acids and N-tosylhydrazone-tethered benzonitriles
10.1021/acs.orglett.8b03705 · 2019 · External reference
Heterocyclization and spirocyclization processes based on domino reactions of N-tosylhydrazones and boronic acids involving intramolecular allylborylations of nitriles
10.1002/chem.201803309 · 2018 · External reference
Stereoselective domino carbocyclizations of γ- and δ-cyano-N-tosylhydrazones with Alkenylboronic acids with formation of two different C(sp3)–C(sp2) bonds on a quaternary stereocenter
10.1021/jacs.6b08116 · 2016 · External reference
Metal-free carbon-carbon bond-forming reductive coupling between boronic acids and tosylhydrazones
10.1038/nchem.328 · 2009 · External reference
The decomposition of toluene-p-sulphonylhydrazones by alkali
10.1039/jr9520004735 · 1952 · External reference
Base and solvent mediated decomposition of tosylhydrazones: highly selective synthesis of N-alkyl substituted hydrazones, dialkylidenehydrazines, and oximes
10.1016/j.tet.2013.03.055 · 2013 · External reference
N-Alkylation of tosylhydrazones via a metal-free reductive coupling procedure
10.1016/j.tetlet.2012.11.124 · 2013 · External reference
Iron(III) phthalocyanine-chloride-catalyzed synthesis of sulfones from sulfonylhydrazones
10.1016/j.tetlet.2016.04.044 · 2016 · External reference
Synthesis of sulfones by iron-catalyzed decomposition of sulfonylhydrazones
10.1002/ejoc.201001492 · 2011 · External reference
Copper-catalyzed nitrogen loss of sulfonylhydrazones: a reductive strategy for the synthesis of sulfones from carbonyl compounds
10.1021/ol101955x · 2010 · External reference
Ruthenium(II) porphyrin catalyzed cyclopropanation of alkenes with tosylhydrazones
10.1016/j.tetlet.2003.09.157 · 2003 · External reference
Wittig ylide mediated decomposition of N-sulfonylhydrazones to sulfinates
10.1021/acs.orglett.7b03953 · 2018 · External reference
Base-promoted direct synthesis of sulfinates from N-sulfonylhydrazones under metal-free conditions
10.1055/s-0039-1690754 · 2020 · External reference
Ethyl glyoxylate N-tosylhydrazone as sulfonyl-transfer reagent in base-catalyzed sulfa-Michael reactions
10.1021/jo402518q · 2014 · External reference
Reactivity profiles of diazo amides, esters, and ketones in transition-metal-free C–H insertion reactions
10.1021/jacs.8b12420 · 2019 · External reference
Transition metal and base free coupling of N-tosylhydrazones with 1, 3-dicarbonyl compound
10.1016/j.tetlet.2017.02.001 · 2017 · External reference
1,3-Dipolar cycloaddition of alkyne-tethered N-tosylhydrazones: synthesis of fused polycyclic pyrazoles
10.1021/acs.joc.6b02076 · 2016 · External reference
Unified approach to pyrazole-fused heterocyclic and carbocyclic motifs through one-pot condensation and intramolecular dipolar cycloaddition reaction
10.1055/s-0035-1562533 · 2016 · External reference
“On water” cascade synthesis of benzopyranopyrazoles and their macrocycles
10.1016/j.tetlet.2018.03.013 · 2018 · External reference
A step-economical route to fused 1,2,3-triazoles via an intramolecular 1,3-dipolar cycloaddition between a nitrile and an in situ generated aryldiazomethane
10.1021/jo5013288 · 2014 · External reference
Oxidative Mizoroki–Heck-type reaction of arylsulfonyl hydrazides for a highly regio- and stereoselective synthesis of polysubstituted alkenes
10.1002/chem.201103671 · 2012 · External reference
Purple acid phosphatase inhibitors as leads for osteoporosis chemotherapeutics
10.1016/j.ejmech.2018.08.004 · 2018 · External reference
A convenient approach to an advanced intermediate toward the naturally occurring, bioactive 6-substituted 5-hydroxy-4-aryl-1H-quinolin-2-ones
10.1039/c5ob02680f · 2016 · External reference
Efficient synthesis of novel 1,2,4-triazole fused acyclic and 21–28 membered macrocyclic and/or lariat macrocyclic oxaazathia crown compounds with potential antimicrobial activity
10.1016/j.ejmech.2010.08.046 · 2010 · External reference
Cinchona alkaloid/sulfinyl chloride combinations: Enantioselective sulfinylating agents of alcohols
10.1021/ja0430189 · 2005 · External reference
