Research graph
References from Sulfenylation of Arenes with Ethyl Arylsulfinates in Water. Local targets link to admitted publications; unresolved targets remain external evidence.
Iron-sulfur cluster biosynthesis: Toward an understanding of cellular machinery and molecular mechanism
10.1021/ar0301781 · 2004 · External reference
A highly selective and sensitive near-infrared fluorescence probe for arylamine N-acetyltransferase 2 in vitro and in vivo
10.1039/c3sc51079d · 2013 · External reference
Fifty years of smelling sulfur
10.1080/17415993.2012.717294 · 2013 · External reference
SAR of 3, 4-Dihydropyrido [3, 2-d] pyrimidone p38 Inhibitors
10.1016/j.bmcl.2003.08.059 · 2003 · External reference
Viracept (Nelfinavir Mesylate, AG1343): A Potent, Orally Bioavailable Inhibitor of HIV-1 Protease
10.1021/jm9704098 · 1997 · External reference
Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
10.1039/b316241a · 2005 · External reference
Bis and tris indole alkaloids from marine organisms: new leads for drug discovery
10.2174/092986707781058904 · 2007 · External reference
Medicinal applications of (benz) imidazole-and indole-based macrocycles
10.1111/cbdd.12802 · 2017 · External reference
Marine indole alkaloids: potential new drug leads for the control of depression and anxiety
10.1021/cr900211p · 2010 · External reference
Novel routes to pyrroles, indoles and carbazoles-applications in natural product synthesis
10.2174/138527205774370496 · 2005 · External reference
Imaging induction of cytoprotective enzymes in intact human cells: coumberone, a metabolic reporter for human AKR1C enzymes reveals activation by panaxytriol, an active component of red ginseng
10.1021/ja801245y · 2008 · External reference
Organosulfur compounds and cardiovascular disease
10.1016/j.mam.2010.09.009 · 2010 · External reference
Transition metal catalyzed synthesis of aryl sulfides
10.3390/molecules16010590 · 2011 · External reference
Metal-catalyzed carbon-sulfur bond formation
10.1021/cr9902749 · 2000 · External reference
Organocatalytic carbon-sulfur bond-forming reactions
10.1021/cr500235v · 2014 · External reference
A general and long-lived catalyst for the palladium-catalyzed coupling of aryl halides with thiols
10.1021/ja0580340 · 2006 · External reference
Cobalt-catalyzed aryl-sulfur bond formation
10.1021/ol062344l · 2006 · External reference
Recent advances in C-S bond formation via C-H bond functionalization and decarboxylation
10.1039/c4cs00239c · 2015 · External reference
Sustainable and site-selective C-H sulfenylation of aromatic compounds with thiol using catalytic graphene oxide and NaI
10.1002/ajoc.201700275 · 2017 · External reference
Sulfenylation of C-H bonds for C-S bond formation under metal-free conditions
10.1002/ejoc.201700853 · 2017 · External reference
Recent advances in the C(sp2)-S bond formation reactions by transition metal-free C(sp2)-H functionalization
10.6023/cjoc201702009 · 2017 · External reference
Progress in iodine-mediated sulfonylation reactions
10.6023/cjoc201504039 · 2015 · External reference
Transition metal-free direct C-H bond sulfenylation of alkenes and arenes
10.6023/cjoc201912044 · 2020 · External reference
Recent advances and prospects of organic reactions “on water”
10.1002/slct.201903360 · 2019 · External reference
Green chemistry oriented organic synthesis in water
10.1039/c1cs15222j · 2012 · External reference
Facile synthesis of 1, 4-diketones via three-component reactions of α-ketoaldehyde, 1, 3-dicarbonyl compound, and a nucleophile in water
10.1039/c7gc03644b · 2018 · External reference
Bifunctional solid catalyst for organic reactions in water: simultaneous anchoring of acetylacetone ligands and amphiphilic ionic liquid “tags” by using a dihydropyran linker
10.1002/asia.201800567 · 2018 · External reference
Utilization of bio-based glycolaldehyde aqueous solution in organic synthesis: application to the synthesis of 2, 3-dihydrofurans
10.1039/c8gc04000a · 2019 · External reference
Catalytic organic reactions in water toward sustainable society
10.1021/acs.chemrev.7b00417 · 2018 · External reference
Green and sustainable solvents in chemical processes
10.1021/acs.chemrev.7b00571 · 2018 · External reference
Bis(imino)pyridine palladium(II) complexes: Synthesis, structure and catalytic activity
10.1016/j.jorganchem.2009.03.021 · 2009 · External reference
Preparation and catalytic properties of bis(imino)pyridine palladium(II) complexes as efficient catalysts for Suzuki cross-coupling reaction in water
10.1002/aoc.1481 · 2009 · External reference
Bis(imino)pyridine palladium(II) complexes as efficient catalysts for the Suzuki-Miyaura reaction in water
10.1002/aoc.1591 · 2010 · External reference
Metallomicelles of palladium(II) complexes as efficient catalysts for the Suzuki-Miyaura reaction in neat water
10.1002/aoc.3021 · 2013 · External reference
Synthesis of terphenyl derivatives by Pd-catalyzed Suzuki-Miyaura reaction of dibromobenzene Using 2N2O-salen as a ligand in aqueous solution
10.1002/cjoc.201500446 · 2015 · External reference
A simple and efficient 2N2O-Cu(II) complex as a catalyst for N-arylation of imidazoles in water
10.1002/aoc.3317 · 2015 · External reference
Water-soluble salen-Pd complex as an efficient catalyst for Suzuki-Miyaura reaction of sterically hindered substrates in pure water
10.1016/j.tet.2015.08.070 · 2015 · External reference
Copper-catalyzed three-component one-pot synthesis of aryl sulfides with sulfur powder under aqueous conditions
10.1002/adsc.201600642 · 2016 · External reference
Odorless, regioselective synthesis of diaryl sulfides and α-thioaryl carbonyls from sodium arylsulfinates via a metal-free radical strategy in water
10.1002/adsc.201600846 · 2016 · External reference
Phenyliodine (III) bis (trifluoroacetate)(PIFA)-mediated synthesis of aryl sulfides in water
10.1021/acs.joc.8b00435 · 2018 · External reference
Cooperative catalysis by bovine serum albumin-iodine towards cascade oxidative coupling-C(sp2)-H sulfenylation of indoles/hydroxyaryls with thiophenols on water
10.1039/c6ob00930a · 2016 · External reference
Cobalt-catalyzed aerobic cross-dehydrogenative coupling of C-H and thiols in water for C-S formation
10.1021/acs.joc.7b02718 · 2018 · External reference
One-pot synthesis of sulphinic esters from disulphides
10.1055/s-1988-27535 · 1988 · External reference
Hypervalent iodine in synthesis XXIV: a facile method for the preparation of arylsulfinic esters: oxidation of disulfides or thiophenols by phenyliodine (III) bis (trifluoroacetate) in the presence of alcohols
10.1080/00397919708006060 · 1997 · External reference
A generalization of the base effect on the diastereoselective synthesis of sulfinic and phosphinic esters
10.1016/s0040-4039(99)00171-9 · 1999 · External reference
An efficient and novel method for the synthesis of sulfinate esters under solvent-free conditions
10.1016/j.tetlet.2006.02.080 · 2006 · 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
tert-Butyl sulfoxide as a starting point for the synthesis of sulfinyl containing compounds
10.1021/acs.orglett.5b02743 · 2015 · External reference
Copper-catalyzed aerobic formation of unstable sulfinyl radicals for the synthesis of sulfinates and thiosulfonates
10.1002/adsc.201500785 · 2016 · 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 oxidative reaction of sulfonyl hydrazides with alcohols: an easy access to sulfinates
10.1002/asia.201501262 · 2016 · External reference
Facial synthesis of sulfinic esters via copper-catalyzed reaction of sulfonyl hydrazides with alcohols in air
10.1016/j.jscs.2018.10.007 · 2019 · External reference
Alkyl sulfinates: formal nucleophiles for synthesizing TosMIC analogs
10.1002/ejoc.201403615 · 2015 · External reference
Unsaturation of ketones, nitriles and lactams with methyl phenylsulfinate
10.1016/0040-4039(95)01461-p · 1995 · External reference
Mild and general method for the synthesis of sulfonamides
10.1055/s-2007-1000850 · 2008 · External reference
Synthesis and arylation of unprotected sulfonimidamides
10.1016/j.tet.2012.06.072 · 2012 · External reference
Methyl sulfinates as electrophiles in Friedel-Crafts reactions. synthesis of aryl sulfoxides
10.1021/jo2006335 · 2011 · External reference
Dramatic influence of ionic liquid and ultrasound irradiation on the electrophilic sulfinylation of aromatic compounds by sulfinic esters
10.3390/molecules22091458 · 2017 · External reference
Preparation of (phenylsulfinyl) phenols from aryl phenylsulfinates: “Thia-Fries rearrangement”
10.1016/0040-4039(95)02068-3 · 1996 · External reference
Preparation of propargylic sulfinates and their [2, 3]-sigmatropic rearrangement to allenic sulfones
10.1002/adsc.201600986 · 2017 · External reference
NH4I/1, 10-phenanthroline catalyzed direct sulfenylation of N-heteroarenes with ethyl arylsulfinates
10.1016/j.tet.2019.130664 · 2019 · External reference
A Sulfone-containing imidazolium-based Brønsted acid ionic liquid catalyst enables replacing dipolar aprotic solvents with butyl acetate
10.1002/adsc.201900246 · 2019 · External reference
Highly selective copper-catalyzed oxidation of benzyl alcohols to aromatic aldehydes in water at room temperature
10.1002/aoc.3473 · 2016 · External reference
Metal-free oxidation of secondary benzylic alcohols using aqueous TBHP
10.1080/00397911.2016.1223307 · 2016 · External reference
Synthesis of novel 1,4-substituted 1,2,3-triazoles by water-soluble (salicyladimine)2Cu complex catalyzed azide-alkyne cycloaddition in water
10.2174/1570178614666170609072912 · 2017 · External reference
A simple, mild and efficient oxidation of benzylic alcohols in the presence of NBS/KOAc in aqueous solution
10.2174/1570178614666170221142818 · 2017 · External reference
Cu(II)-Catalyzed ligand-free oxidation of diarylmethanes and second alcohols in water
10.1002/cjoc.201700115 · 2017 · External reference
Novel non-toxic and non-hazardous solvent systems for the chemistry of indoles: use of a sulfone-containing Brønsted acid ionic liquid catalyst in butyl acetate
10.1002/cctc.201900784 · 2019 · External reference
Brönsted acidic ionic liquid catalyzed synthesis of benzo[a]carbazole from renewable acetol and 2-phenylindoles in a biphasic system
10.1016/s1872-2067(19)63370-x · 2019 · External reference
Aldo-X bifunctional building blocks for the synthesis of heterocycles
10.1002/tcr.201600042 · 2017 · External reference
Brønsted acid ionic liquid as a solvent-conserving catalyst for organic reactions
10.1002/cssc.201402220 · 2014 · External reference
Lewis acid-catalyzed synthesis of benzofurans and 4, 5, 6, 7-tetrahydrobenzofurans from acrolein dimer and 1, 3-dicarbonyl compounds
10.1021/acs.joc.9b00270 · 2019 · External reference
Biomass-derived solvents for sustainable transition metal-catalyzed C-H activation
10.1021/acssuschemeng.9b00226 · 2019 · External reference
Towards sustainable C-H functionalization reactions: The emerging role of bio-based reaction media
10.1002/chem.201801114 · 2018 · External reference
A tailored polymeric cationic tag-anionic Pd(II) complex as a catalyst for the low-leaching Heck-Mizoroki coupling in flow and in biomass-derived GVL
10.1039/c8gc03228a · 2019 · External reference
A conjugate Lewis base-Brønsted acid catalyst for the sulfenylation of nitrogen containing heterocycles under mild conditions
10.1039/c6cc09998j · 2017 · External reference
Iodine-catalyzed regioselective sulfenylation of indoles with sodium sulfinates
10.1002/adsc.201300773 · 2014 · External reference
Direct, metal-free C(sp2)-H chalcogenation of indoles and imidazopyridines with dichalcogenides catalysed by KIO3
10.1002/chem.201705404 · 2018 · External reference
Flavin-iodine coupled organocatalysis for the aerobic oxidative direct sulfenylation of indoles with thiols under mild conditions
10.1039/c8gc00117k · 2018 · External reference
Nitrosonium ion catalysis: aerobic, metal-free cross-dehydrogenative carbon-heteroatom bond formation
10.1039/c8cc08328b · 2018 · External reference
Graphene oxide mediated thiolation of indoles in water: a green and sustainable approach to synthesize 3-sulfenylindoles
10.1039/c8qo00726h · 2019 · External reference
Catalyst-free thiolation of indoles with sulfonyl hydrazides for the synthesis of 3-sulfenylindoles in water
10.1039/c6gc00313c · 2016 · External reference
N-Hydroxy sulfonamides as new sulfenylating agents for the functionalization of aromatic compounds
10.1039/c7ob01390f · 2017 · External reference
Copper (I)-catalyzed thiolation of C-H bonds for the synthesis of sulfenyl pyrroles and indoles
10.1055/s-0037-1610295 · 2019 · External reference
Acid-induced chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates: the reducibility of halide anions in [Hmim] Br
10.1039/c6ob02823c · 2017 · External reference
Disproportionate coupling reaction of sodium sulfinates mediated by BF3·OEt2: an approach to symmetrical/unsymmetrical thiosulfonates
10.1021/acs.orglett.8b01808 · 2018 · External reference
Catalyst-free sulfenylation of indoles with sulfinic esters in ethanol
10.1039/c8gc01764f · 2018 · External reference
Iodine-PPh3-mediated C3-sulfenylation of indoles with sodium sulfinates
10.1039/c4ra02607a · 2014 · 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
Scandium-catalyzed electrophilic alkene difunctionalization: regioselective synthesis of thiosulfone derivatives
10.1039/c9qo00138g · 2019 · External reference
Cu-catalyzed direct C-H thiolation of electron-rich arenes with arylsulfonyl hydrazides
10.1016/j.tet.2018.02.014 · 2018 · External reference
Iodine-Mediated Thiolation of substituted naphthols/naphthylamines and arylsulfonyl hydrazides via C(sp2)-H bond functionalization
10.1021/jo501778h · 2014 · External reference
CoII immobilized on an aminated magnetic metal-organic framework catalyzed C-N and C-S bond forming reactions: a journey for the mild and efficient synthesis of arylamines and arylsulfides
10.1039/c9nj03400e · 2019 · External reference
