Research graph
References from B(C6F5)3-Catalyzed C–C Coupling of 1,4-Naphthoquinones with the C-3 Position of Indole Derivatives in Water. Local targets link to admitted publications; unresolved targets remain external evidence.
Palladium-Catalyzed Intramolecular Coupling of 2-[(2-Pyrrolyl)silyl]aryl Triflates through 1,2-Silicon Migration
10.1021/ja901622b · 2009 · External reference
Silicon-based cross-coupling reaction: an environmentally benign version
10.1039/c1cs15122c · 2011 · External reference
Palladium-catalysed cross-coupling of organosilicon reagents
10.1039/c1cs15181a · 2012 · External reference
Catalytic Friedel-Crafts C-H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes
10.1002/anie.201611536 · 2017 · External reference
Organic Dye-Sensitized Ionic Liquid Based Solar Cells: Remarkable Enhancement in Performance through Molecular Design of Indoline Sensitizers
10.1002/anie.200705225 · 2008 · External reference
Synthesis and chemistry of melatonin and of related compounds. A review
10.1080/00304949509458177 · 1995 · External reference
Unresolved reference
2002 · External reference
Organosilicon molecules with medicinal applications
10.1021/jm3010114 · 2013 · External reference
Design, synthesis, and biological evaluation of indoline and Indole derivatives as potent and selective α1A-adrenoceptor antagonists
10.1021/acs.jmedchem.5b02023 · 2016 · External reference
Synthesis and functionalization of indoles through palladium-catalyzed reactions
10.1021/cr040639b · 2005 · External reference
Chemistry of the hexahydropyrrolo[2,3-b]indoles: configuration, conformation, reactivity, and applications in synthesis
10.1021/ar050175j · 2007 · External reference
Metabolic Products of Aspergillus terreus. X.: Biosynthesis of Asterriquinones
10.1248/cpb.38.2929 · 1990 · External reference
Relationship between the structure and cytotoxic activity of asterriquinone, an antitumor metabolite of Aspergillus terreus, and its alkyl ether derivatives
10.1248/bpb.21.945 · 1998 · External reference
Methyl scanning: total synthesis of demethylasterriquinone B1 and derivatives for identification of sites of interaction with and isolation of its receptor
10.1021/ja044325h · 2005 · External reference
Organometallic Routes to 2,5-Dihydroxy-3-(indol-3-yl)benzoquinones. Synthesis of Demethylasterriquinone B4
10.1021/jo048126s · 2005 · External reference
Bi(OTf)3-catalyzed conjugate addition of indoles to p-quinones: a facile synthesis of 3-indolyl quinones
10.1016/j.tetlet.2003.10.041 · 2003 · External reference
InBr3-Catalyzed conjugate addition of indoles to p-quinones: an efficient synthesis of 3-indolylquinones
10.1055/s-2003-44364 · 2004 · External reference
Reaction of Some Indoles with 1, 4-Naphthoquinones in the Presence of Pd (OAc)2
10.1002/jhet.2000 · 2014 · External reference
Copper (II) Bromide–Catalyzed Conjugate Addition of Indoles to α, β-Enones
10.1080/00397910500518940 · 2006 · External reference
Synthesis of 2, 5-dihydroxy-3-(indol-3-yl) benzoquinones by acid-catalyzed condensation of indoles with 2, 5-dichlorobenzoquinone
10.1021/jo0204597 · 2002 · External reference
152. Melanin and its precursors. Part II. Model experiments on the reactions between quinones and indoles, and consideration of a possible structure for the melanin polymer
10.1039/jr9510000703 · 1951 · External reference
Synthesis of 3-indolyl-2, 5-dihydroxybenzoquinones
10.1021/ol006852l · 2001 · External reference
Synthesis of 2-(3-indolyl)-1,4-naphthoquinones using 3-iodoindoles
10.1002/jhet.5570420625 · 2005 · External reference
Parallel Synthesis of Indolylquinones and Their Cell-Based Insulin Mimicry
10.1021/cc070062m · 2007 · External reference
Promotion of organic reactions by interfacial hydrogen bonds on hydroxyl group rich nano-solids
10.1039/b801361f · 2008 · External reference
Heterogeneously Catalyzed Domino Synthesis of 3-Indolylquinones Involving Direct Oxidative C–C Coupling of Hydroquinones and Indoles
10.1021/acsomega.7b00201 · 2017 · External reference
“On Water”-Promoted Direct Coupling of Indoles with 1,4-Benzoquinones without Catalyst
10.1002/ejoc.200500863 · 2006 · External reference
Sustainable production of chemicals an educational perspective
10.1039/c2rp90002e · 2012 · External reference
Sustainable development and green chemistry in chemistry education
10.1039/c2rp90003c · 2012 · External reference
China’s road to sustainability
10.1126/science.1186234 · 2010 · External reference
Education for a sustainable future
10.1126/science.1143552 · 2007 · External reference
The Green ChemisTREE: 20 years after taking root with the 12 principles
10.1039/c8gc00482j · 2018 · External reference
Green chemistry oriented organic synthesis in water
10.1039/c1cs15222j · 2012 · External reference
Green chemistry: principles and practice
10.1039/b918763b · 2010 · External reference
Palladium and copper-catalysed arylation reactions in the presence of water, with a focus on carbon–heteroatom bond formation
10.1039/b709565c · 2008 · External reference
Practical approaches to green solvents
10.1126/science.1069622 · 2002 · External reference
How do the fine chemical, pharmaceutical, and related industries approach green chemistry and sustainability?
10.1039/c1gc15904f · 2012 · External reference
Transition metal free oxygenation of 8-aminoquinoline amides in water
10.1039/c8gc00191j · 2018 · External reference
Conservative evolution and industrial metabolism in Green Chemistry
10.1039/c8gc00514a · 2018 · External reference
Controlled mono-olefination versus diolefination of arenes via C-H activation in water: a key role of catalysts
10.1039/c8gc00790j · 2018 · External reference
Suzuki-Miyaura Cross-Coupling Reactions in Aqueous Media: Green and Sustainable Syntheses of Biaryls
10.1002/cssc.200900221 · 2010 · External reference
Recyclable heterogeneous palladium catalysts in pure water: Sustainable developments in Suzuki, Heck, Sonogashira and Tsuji-Trost reactions
10.1002/adsc.200900765 · 2010 · External reference
Chiral Copper(II)-Catalyzed Enantioselective Boron Conjugate Additions to α,β-Unsaturated Carbonyl Compounds in Water
10.1002/anie.201207343 · 2012 · External reference
Organic synthesis reactions on-water at the organic-liquid water interface
10.1039/c6ob01724j · 2016 · External reference
Stereoselective organic reactions in water
10.1021/cr010122p · 2002 · External reference
Development of novel Lewis acid catalysts for selective organic reactions in aqueous media
10.1021/ar000145a · 2002 · External reference
Organic chemistry in water
10.1039/b507207g · 2006 · External reference
Reactions of C-H bonds in water
10.1021/cr050980b · 2007 · External reference
Water-promoted C-S bond formation reactions
10.1038/s41467-018-03698-8 · 2018 · External reference
Chemoselective Silylative Reduction of Conjugated Nitriles under Metal-Free Catalytic Conditions: β-Silyl Amines and Enamines
10.1002/anie.201502366 · 2015 · External reference
Cocatalysts for metal-catalyzed olefin polymerization: activators, activation processes, and structure-activity relationships
10.1021/cr980462j · 2000 · External reference
Pentafluorophenylboranes: from obscurity to applications
10.1039/cs9972600345 · 1997 · External reference
Nonmetal catalyzed hydrogenation of carbonyl compounds
10.1021/ja5088979 · 2014 · External reference
Metal-Free Hydrogenation Catalyzed by an Air-Stable Borane: Use of Solvent as a Frustrated Lewis Base
10.1002/anie.201405531 · 2014 · External reference
Chemoselective deoxygenation of ether-substituted alcohols and carbonyl compounds by B(C6F5)3-catalyzed reduction with (HMe2SiCH2)2
10.1039/c8cc01163j · 2018 · External reference
Borane-catalyzed transfer hydrogenations of pyridines with ammonia borane
10.1021/acs.orglett.6b02610 · 2016 · External reference
Enabling catalytic ketone hydrogenation by frustrated Lewis pairs
10.1021/ja508829x · 2014 · External reference
Nonmetal catalyzed hydrogenation of carbonyl compounds
10.1021/ja5088979 · 2014 · External reference
Metal-Free Hydrogenation Catalyzed by an Air-Stable Borane: Use of Solvent as a Frustrated Lewis Base
10.1002/anie.201405531 · 2014 · External reference
Borane-catalyzed transfer hydrogenations of pyridines with ammonia borane
10.1021/acs.orglett.6b02610 · 2016 · External reference
Chemoselective deoxygenation of ether-substituted alcohols and carbonyl compounds by B(C6F5)3-catalyzed reduction with (HMe2SiCH2)2
10.1039/c8cc01163j · 2018 · External reference
Direct observation of a borane-silane complex involved in frustrated Lewis-pair-mediated hydrosilylations
10.1038/nchem.2063 · 2014 · External reference
Tris(pentafluorophenyl) boron-catalyzed hydrosilation of aromatic aldehydes, ketones, and esters
10.1021/ja961536g · 1996 · External reference
Boron-catalyzed aromatic C-H bond silylation with hydrosilanes
10.1021/jacs.6b01349 · 2016 · External reference
Non-metal-catalyzed heterodehydrocoupling of phosphines and hydrosilanes: mechanistic studies of B(C6F5)3-mediated formation of P-Si bonds
10.1021/jacs.7b09175 · 2017 · External reference
Catalytic metal-free Si-N cross-dehydrocoupling
10.1039/c3cc49558b · 2014 · External reference
Frustrated lewis pair catalyzed dehydrogenative oxidation of indolines and other heterocycles
10.1002/anie.201606426 · 2016 · External reference
Boron-catalyzed aromatic C-H bond silylation with hydrosilanes
10.1021/jacs.6b01349 · 2016 · External reference
A unified survey of Si-H and H-H bond activation catalysed by electron-deficient boranes
10.1039/c4cs00451e · 2015 · External reference
Formal SiH4 chemistry using stable and easy-to-handle surrogates
10.1038/nchem.2329 · 2015 · External reference
Selective Silylative Reduction of Pyridines Leading to Structurally Diverse Azacyclic Compounds with the Formation of sp3 C-Si Bonds
10.1021/jacs.5b09209 · 2015 · External reference
Cross-coupling of primary amides to aryl and heteroaryl partners using (DiMeIHeptCl) Pd promoted by trialkylboranes or B(C6F5)3
10.1021/jacs.7b09488 · 2017 · External reference
Enantioselective Conia-Ene-Type Cyclizations of Alkynyl Ketones through Cooperative Action of B(C6F5)3, N-Alkylamine and a Zn-Based Catalyst
10.1021/jacs.8b13757 · 2019 · External reference
The broadening reach of frustrated Lewis pair chemistry
10.1126/science.aaf7229 · 2016 · External reference
Frustrated lewis pairs
10.1021/jacs.5b06794 · 2015 · External reference
Frustrated Lewis pairs: from concept to catalysis
10.1021/ar500375j · 2015 · External reference
Frustrated Lewis pairs catalyzed asymmetric metal-free hydrogenations and hydrosilylations
10.1021/acs.accounts.7b00530 · 2018 · External reference
Coordination-induced weakening of ammonia, water, and hydrazine X–H bonds in a molybdenum complex
10.1126/science.aag0246 · 2016 · External reference
Tetrahydroxydiboron-Mediated Palladium-Catalyzed Transfer Hydrogenation and Deuteriation of Alkenes and Alkynes Using Water as the Stoichiometric H or D Atom Donor
10.1021/jacs.6b02132 · 2016 · External reference
Aqua, alcohol, and acetonitrile adducts of tris (perfluorophenyl) borane: evaluation of Brønsted acidity and ligand lability with experimental and computational methods
10.1021/ja001915g · 2000 · External reference
Equilibria in the B(C6F5)3-H2O system: synthesis and crystal structures of H2O·B(C6F5)3 and the anions [HOB(C6F5)3]- and [(F5C6)3B(μ-OH) B(C6F5)3]-
10.1039/a804918a · 1998 · External reference
Boron-Catalyzed O-H Bond Insertion of α-Aryl α-Diazoesters in Water
10.1021/acs.orglett.8b01988 · 2018 · External reference
Separating electrophilicity and Lewis acidity: The synthesis, characterization, and electrochemistry of the electron deficient tris(aryl)boranes B(C6F5)3-n (C6Cl5)n (n = 1-3)
10.1021/ja205037t · 2011 · External reference
Aqua, alcohol, and acetonitrile adducts of tris(perfluorophenyl)borane: evaluation of Brønsted acidity and ligand lability with experimental and computational methods
10.1021/ja001915g · 2000 · External reference
B(C6F5)3-Catalyzed Regioselective Deuteration of Electron-Rich Aromatic and Heteroaromatic Compounds
10.1021/acs.orglett.7b02701 · 2017 · External reference
Mechanism of Boron-Catalyzed N-Alkylation of Primary and Secondary Arylamines with Ketones Using Silanes under “Wet” Conditions
10.1021/acs.organomet.8b00405 · 2018 · External reference
Facile Protocol for Water-Tolerant “Frustrated Lewis Pair”-Catalyzed Hydrogenation
10.1021/acscatal.5b01417 · 2015 · External reference
Tris(pentafluorophenyl)borane-Promoted Stereoselective Glycosylation with Glycosyl Trichloroacetimidates under Mild Conditions
10.1021/acs.joc.8b00215 · 2018 · External reference
Synthesis of Aryl-Substituted 1, 4-Benzoquinone via Water-Promoted and In(OTf)3-Catalyzed in situ Conjugate Addition-Dehydrogenation of Aromatic Compounds to 1, 4-Benzoquinone in Water
10.1002/adsc.200505248 · 2006 · External reference
C-H Functionalization of 1, 4-Naphthoquinone by Oxidative Coupling with Anilines in the Presence of a Catalytic Quantity of Copper(II) Acetate
10.1021/jo200354u · 2011 · External reference
Practical C-H Functionalization of Quinones with Boronic Acids
10.1021/ja111152z · 2011 · External reference
Tandem oxidation–oxidative C-H/C-H cross-coupling: synthesis of arylquinones from hydroquinones
10.1039/c3cc41067f · 2013 · External reference
Sequential, One-Pot Access to Arylated Benzoquinones/Naphthoquinones from Phenols/Naphthols
10.1002/ejoc.201600119 · 2016 · External reference
