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A route to 2-substituted tetrahydroquinolines via palladium-catalyzed intramolecular hydroamination of anilino-alkynes.Tunneling Desorption of Single Hydrogen on the Surface of Titanium Dioxide.Manganese powder promoted highly efficient and selective synthesis of fullerene mono- and biscycloadducts at room temperatureRecent progress in the catalytic synthesis of imidazoles.Coinage metal-assisted synthesis of heterocycles.Gold nanoparticle (AuNPs) and gold nanopore (AuNPore) catalysts in organic synthesis.Synthesis of extended polycyclic aromatic hydrocarbons by oxidative tandem spirocyclization and 1,2-aryl migration.Gold-catalyzed alkylation of silyl enol ethers with ortho-alkynylbenzoic acid esters.Triflic acid catalyzed synthesis of spirocycles via acetylene cations.TfOH-catalyzed intramolecular alkyne-ketone metathesis leading to highly substituted five-membered cyclic enones.Iodine-mediated electrophilic cyclization of 2-alkynyl-1-methylene azide aromatics leading to highly substituted isoquinolines and its application to the synthesis of norchelerythrine.Synthesis of 5-substituted 1H-tetrazoles by the copper-catalyzed [3+2] cycloaddition of nitriles and trimethylsilyl azide.Ni-Catalyzed direct 1,4-difunctionalization of [60]fullerene with benzyl bromides.Solvent-controlled stereoselective formation of a cyclic ether in the lewis acid-mediated allylation of an alpha-chloroacetoxy acyclic ether. Very high stereoselectivity in CH3CN vs low stereoselectivity in CH2Cl2.Palladium-Catalyzed sp2-sp3 Coupling of Chloromethylarenes with Allyltrimethoxysilane: Synthesis of Allyl Arenes.Synthesis of 5H-Dibenzo[c,e]azepine-5,7(6H)-diones from Benzamides via Palladium-Catalyzed Double C-H Bond Activation.Highly efficient heterogeneous aerobic cross-dehydrogenative coupling via C-H functionalization of tertiary amines using a nanoporous gold skeleton catalyst.Biphenyl end-capped bithiazole co-oligomers for high performance organic thin film field effect transistors.2-Positional pyrene end-capped oligothiophenes for high performance organic field effect transistors.Synthesis of allylated quinolines/isoquinolines via palladium-catalyzed cyclization-allylation of azides and allyl methyl carbonate.Unsupported Nanoporous Gold Catalyst for Chemoselective Hydrogenation Reactions under Low Pressure: Effect of Residual Silver on the Reaction.Brønsted acid-catalyzed cascade cycloisomerization of enynes via acetylene cations and sp3-hybridized C-H bond activation.Rhodium-Catalyzed Oxidative Benzannulation of N-Adamantyl-1-naphthylamines with Internal Alkynes via Dual C-H Bond Activation: Synthesis of Substituted Anthracenes.Copper-Catalyzed Aza-Diels-Alder Reaction and Halogenation: An Approach To Synthesize 7-Halogenated Chromenoquinolines.Cu-catalyzed C-H amination of hydrofullerenes leading to 1,4-difunctionalized fullerenes.Pd-Catalyzed Consecutive C-H Arylation Triggered Cyclotrimerization: Synthesis of Star-shaped Benzotristhiazoles and Benzotrisoxazoles.Remarkable catalytic property of nanoporous gold on activation of diborons for direct diboration of alkynes.Deuterium Isotope Effect on Bulk Heterojunction Solar Cells. Enhancement of Organic Photovoltaic Performances Using Monobenzyl Substituted Deuteriofullerene AcceptorsNanostructured Materials as Catalysts: Nanoporous-Gold-Catalyzed Oxidation of Organosilanes with WaterAerobic oxidation of alcohols in the liquid phase with nanoporous gold catalystsNanoporous Gold Catalyst for Highly Selective Semihydrogenation of Alkynes: Remarkable Effect of Amine AdditivesA nanostructured skeleton catalyst: Suzuki-coupling with a reusable and sustainable nanoporous metallic glass Pd-catalystMetal-Free Decarboxylative Alkoxylation of 2-Picolinic Acid and Its Derivatives with Cyclic Ethers: One Step Construction of C-O and C-Cl BondsPalladium-Catalyzed Ligand-Controlled Regioselective Nucleophilic Aromatic Substitution of 1-(Chloromethyl)naphthalenes with ArylacetonitrilesTransition-Metal-Free Decarboxylative Arylation of 2-Picolinic Acids with Arenes under Air ConditionsMechanism and chemoselectivity of the Pd(II)-catalyzed allylation of aldehydes: a density functional theory studyGold- and indium-catalyzed synthesis of 3- and 6-sulfonylindoles from ortho-alkynyl-N-sulfonylanilinesPtBr2-catalyzed transformation of allyl(o-ethynylaryl)carbinol derivatives into functionalized indenes. Formal sp3 C-H bond activationAn efficient, facile, and general synthesis of 1h-indazoles by 1,3-dipolar cycloaddition of arynes with diazomethane derivativesSynthesis of imidazoles through the copper-catalyzed cross-cycloaddition between two different isocyanides
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Q33291084-9850123C-9DF9-4C71-A19E-59D5D064F0D4Q35687110-85BB91E9-4E87-425E-B7D2-AD8668E7D5F7Q36039927-59D29B57-3AB0-49F1-8725-3078B8772582Q36804297-FBCF05D5-6665-4043-BBE3-8F303141D28EQ37210466-FD22F282-CEFB-4033-AABB-FDB2F2578103Q38187824-26B8FB02-BDA4-4C87-B03A-A3D7FA287B3DQ41926874-ADBFE0F7-7D54-4117-BB2C-17FAD0D6B497Q42154472-ACA12D04-0D21-4232-952D-820BC171B7A9Q45937397-EEC13DD7-0E2C-4E03-9845-501F04586086Q45971901-C2686CC6-8F63-4E5B-93D6-AAC4A9CC04FEQ46303966-AD0B0DD4-BF6E-49EB-89A5-AE592C9E522AQ46534230-1B360D52-354B-40CE-9DD3-92A666E74C62Q46760574-2D38B6BD-0A5B-4562-BB8F-F9521FC55C09Q46964299-2860B91E-0C85-4F11-A582-D8FC097EFDD5Q48176160-91C29167-13D2-4B30-BE7D-05C56D2D3BEBQ48309653-00AF4408-91A8-4DB7-A205-82298F0539F6Q50260781-C94B0DF9-13DF-44AB-83B8-E2726D0DD6C7Q50428284-C9FD2927-6EB4-4712-99F2-E903C825A541Q50428485-5401A264-F212-4178-B4B3-9D53EA89CDD4Q51013552-CA979BEF-373C-480B-80CD-1EFF0E7E45F2Q53059605-38DFFEA9-B0B4-4E0C-A958-6B887365267EQ53332587-65BF7974-B290-4190-AECC-120A9C09D0A7Q53780525-5E7888CE-DD57-4936-86D0-F0EC46DC9DA6Q53958551-4B4DBFCF-EF57-49CB-9798-AE3D93BCB86FQ54385649-9BE32D65-87AC-492D-A870-0C95A76295FDQ54509945-440F5F88-14A6-4176-BBAC-3186555E81AFQ54695898-A78C7EA5-F2EB-46BD-80A3-B0D9349D8493Q56998028-6B305A51-19D3-4C45-8A9F-47E443254333Q57726456-01CB56E9-0BB7-4ADC-8B19-C12CF0BE9A56Q57726488-BE43E829-BF31-420E-BAD8-AE62CD9BE6C8Q57726530-B8EFE5DC-5DD4-4408-9057-0AB4365A4825Q57726552-F66FCA08-BD64-4A95-981B-957377891BA8Q57816029-87ACFAFF-8480-4A17-9ED4-0127AE1F1B47Q58617117-EDAC73AB-07FA-44E0-8E87-6F6AB5A35DB6Q58617744-786C4A7B-D697-475D-8BB6-CE716E0A7EC1Q79662487-898E5DEC-12A9-4BBA-A760-A504739B8D72Q79909556-92184EC9-9BEF-405E-BE19-DC69816C339CQ80004650-8AA2DED7-7D19-42F0-844C-42FFF006C647Q80039161-D9289ED8-B874-460F-9D0F-1838D804CBFAQ80117204-E202E796-B319-4A10-9143-0241FBC09EDB
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Yoshinori Yamamoto
@en
Yoshinori Yamamoto
@nl
type
label
Yoshinori Yamamoto
@en
Yoshinori Yamamoto
@nl
prefLabel
Yoshinori Yamamoto
@en
Yoshinori Yamamoto
@nl
P31
P496
0000-0001-9411-783X