about
Stereoselective hydrothiolation of alkynes catalyzed by cesium base: facile access to (Z)-1-alkenyl sulfides.1-Alkynylphosphines and their derivatives as key starting materials in creating new phosphines.Copper-catalyzed anti-hydrophosphination reaction of 1-alkynylphosphines with diphenylphosphine providing (Z)-1,2-diphosphino-1-alkenes.Synthesis of 2-indolylphosphines by palladium-catalyzed annulation of 1-alkynylphosphine sulfides with 2-iodoanilines.Optimized synthesis, structural investigations, ligand tuning and synthetic evaluation of silyloxy-based alkyne metathesis catalysts.Increasing the structural span of alkyne metathesis.Total synthesis of nominal gobienine A.Synthesis of bulky arylphosphanes by rhodium-catalyzed formal [2+2+2] cycloaddition reaction and their use as ligands.Brønsted Base-Catalyzed Umpolung Intramolecular Cyclization of Alkynyl Imines.Synthesis of bulky phosphines by rhodium-catalyzed formal [2+2+2] cycloaddition reactions of tethered diynes with 1-alkynylphosphine sulfides.Carbocupration of 1-alkynylphosphines followed by trapping with electrophiles.Palladium-catalyzed anti-hydrothiolation of 1-alkynylphosphines.Enantioselective Formal [3+2] Cycloaddition of Epoxides with Imines under Brønsted Base Catalysis: Synthesis of 1,3-Oxazolidines with Quaternary Stereogenic Center.Enantioconvergent Nucleophilic Substitution Reaction of Racemic Alkyne-Dicobalt Complex (Nicholas Reaction) Catalyzed by Chiral Brønsted Acid.Intramolecular addition of benzyl anion to alkyne utilizing [1,2]-phospha-Brook rearrangement under Brønsted base catalysis.Kinetic resolution of racemic amino alcohols through intermolecular acetalization catalyzed by a chiral Brønsted acid.Generation and Application of Homoenolate Equivalents Utilizing [1,2]-Phospha-Brook Rearrangement under Brønsted Base Catalysis.Synthesis of 2,3-allenylamides utilizing [1,2]-phospha-Brook rearrangement and their application to gold-catalyzed cycloisomerization providing 2-aminofuran derivatives.Enantioselective direct Mannich-type reactions of 2-benzylpyridine N-oxides catalyzed by chiral bis(guanidino)iminophosphorane organosuperbase.Chiral Brønsted acid-catalyzed enantioselective Friedel-Crafts reaction of 2-methoxyfuran with aliphatic ketimines generated in situ.Efficient Synthesis of Polysubstituted Pyrroles Based on [3+2] Cycloaddition Strategy Utilizing [1,2]-Phospha-Brook Rearrangement under Brønsted Base CatalysisBrønsted Base-Catalyzed Reductive Cyclization of Alkynyl α-Iminoesters through Auto-Tandem CatalysisOrganocatalytic Arylation of α-Ketoesters Based on Umpolung Strategy: Phosphazene-Catalyzed SN Ar Reaction Utilizing [1,2]-Phospha-Brook RearrangementChiral Brønsted acid-catalyzed intramolecular S2' reaction for enantioselective construction of a quaternary stereogenic centerSynthesis of Enantioenriched γ-Amino-α,β-unsaturated Esters Utilizing Palladium-Catalyzed Rearrangement of Allylic Carbamates for Direct Application to Formal [3 + 2] CycloadditionConstruction of Vicinal Quaternary Stereogenic Centers by Enantioselective Direct Mannich-Type Reaction Using a Chiral Bis(guanidino)iminophosphorane CatalystBrønsted base-catalyzed three-component coupling reaction of α-ketoesters, imines, and diethyl phosphite utilizing [1,2]-phospha-Brook rearrangementEnantioselective intramolecular cyclization of alkynyl esters catalyzed by a chiral Brønsted base.Enantioselective Addition of a 2-Alkoxycarbonyl-1,3-dithiane to Imines Catalyzed by a Bis(guanidino)iminophosphorane OrganosuperbaseRing Expansion of Epoxides under Brønsted Base Catalysis: Formal [3+2] Cycloaddition of β,γ-Epoxy Esters with Imines Providing 2,4,5-Trisubstituted 1,3-OxazolidinesSynthesis of Phenanthrene Derivatives by Intramolecular Cyclization Utilizing the [1,2]-Phospha-Brook Rearrangement Catalyzed by a Brønsted BaseIntramolecular Cyclization of Alkynyl α-Ketoanilide Utilizing [1,2]-Phospha-Brook Rearrangement Catalyzed by Phosphazene BaseBrønsted Base Catalyzed [2,3]-Wittig/Phospha-Brook Tandem Rearrangement SequencePhosphazene-catalyzed intramolecular cyclization of nitrogen-tethered alkynyl estersPalladium-Catalyzed Alkynylthiolation of Alkynes with Triisopropylsilylethynyl SulfideCatalysis-Based and Protecting-Group-Free Total Syntheses of the Marine Oxylipins Hybridalactone and the Ecklonialactones A, B, and CPalladium-Catalyzed Addition of Silyl-Substituted Chloroalkynes to Terminal AlkynesRegio- and Stereoselective Hydroamidation of 1-Alkynylphosphine Sulfides Catalyzed by Cesium BaseIntermolecular Radical Addition of Alkylthio- and Arylthiodiphenylphosphines to Terminal AlkynesDevelopment of Chiral Ureates as Chiral Strong Brønsted Base Catalysts
P50
Q34437870-4CE223FE-DDE7-4D40-8056-AAFA49522604Q37671751-8D30228E-BD90-46FD-BA75-0BCF80E74EE1Q42168060-0AF5BFED-F6D6-400D-BC0F-D23628A3F98CQ43141832-ACA6704D-EB50-4E91-992E-3CEDA7966190Q43708500-E0D271C3-424A-411F-A231-BD040AF3E4B0Q44157152-BBD3EA7C-43B4-4C42-A423-3A8C9FD30B9DQ45898376-AC4A93F6-2598-45A4-8F31-5B33E4BBCDAEQ46498999-704B4D9B-4BEB-4EA6-8C8E-597D0806673CQ50008090-7F0C687E-6140-4D4E-9787-33AE09EBBC7FQ51006126-728895A2-682B-492F-9ECF-1D8CE4500683Q51024236-A8B0C893-E272-42CA-901B-C745EB0A77DDQ51055386-9EDA7951-04E8-4130-BDD5-557AD0B9A357Q52592299-3AD7CD64-29FD-4154-A915-C72A8AE6B65CQ52983172-22A11996-1098-4CBF-850C-9C5322837545Q53092900-149CD0F5-7793-4572-9C08-5EA6C1419CC0Q53639791-759263B0-15C4-432F-AB19-F51425A3B078Q53647477-9403698F-E711-4A6B-AD09-4AE7BD5F920AQ53737839-A1ED2036-84B9-4E14-9050-97C1D43B27C5Q55073787-313C5217-1918-4554-B3C8-892273B5E2EAQ55087206-5101D276-2DA6-4D5B-92F6-13D67FE9E2D6Q62082614-1E841127-E9E8-4EAE-9A0C-53AFEF8ECB78Q62082616-04ED9085-6A8A-4656-A689-1D2F57CEADD7Q62082619-F4DFD13C-CF2A-4A3C-B4F0-D77361601929Q62082623-4739F5FB-62AC-41BD-A35C-BC1D3B2F3306Q62082624-76B4BAD8-B9F8-4963-8099-8DDA1E2F3F52Q62082628-62BEBF85-06F7-4259-AA19-26D0AC77C29BQ62082630-588E29BB-DCD3-4253-84CB-573B4232301FQ62082632-75E568D1-EE0E-4122-A107-1B38606D04E9Q62082634-EA7342A3-1C43-46CF-BCA9-5B2BAED165A5Q62082635-3C885267-CBD4-4685-9F39-4046B6B727F8Q62082636-D93EB850-E185-4342-AD58-E9517FBAB958Q62082642-F956E27D-68AE-4E8B-A1F7-9A7B6F529BC1Q62082644-5AC79CA5-5E90-4779-AF6A-863C826F5887Q62082646-A2CBD8C5-7ADD-44F1-A813-B7FBEDE1FFCAQ62082648-AB0B27B9-F306-4F67-84CB-293C6D20C54AQ62082651-F33AF00D-8D72-41C8-B05B-C4C9472B5642Q62082653-2E380139-3347-4395-B61D-8CCAE1C903E1Q62082657-08D7A47D-D376-4436-A19B-C06A100714A1Q62082661-AC9DEDE3-5BC8-4069-922A-3F7FCAFEABF1Q89648325-34EEBAEC-2B2E-4E10-99C8-7705B538B298
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Azusa Kondoh
@ast
Azusa Kondoh
@en
Azusa Kondoh
@es
Azusa Kondoh
@nl
Azusa Kondoh
@sl
type
label
Azusa Kondoh
@ast
Azusa Kondoh
@en
Azusa Kondoh
@es
Azusa Kondoh
@nl
Azusa Kondoh
@sl
prefLabel
Azusa Kondoh
@ast
Azusa Kondoh
@en
Azusa Kondoh
@es
Azusa Kondoh
@nl
Azusa Kondoh
@sl
P106
P21
P31
P496
0000-0001-7227-8579
P569
2000-01-01T00:00:00Z