about
Catalytic Formal Homo-Nazarov CyclizationPhotocatalytic redox reactions for in-source peptide fragmentation.Total synthesis of (-)-pseudolaric acid BSynthesis of (carbo)nucleoside analogues by [3+2] annulation of aminocyclopropanes.In situ tether formation from amines and alcohols enabling highly selective Tsuji-Trost allylation and olefin functionalizationBenziodoxole-based hypervalent iodine reagents for atom-transfer reactions.Cyclic Hypervalent Iodine Reagents for Atom-Transfer Reactions: Beyond Trifluoromethylation.Total synthesis and biological evaluation of jerantinine E.Catalytic selective cyclizations of aminocyclopropanes: formal synthesis of aspidospermidine and total synthesis of goniomitine.Zinc-gold cooperative catalysis for the direct alkynylation of benzofurans.Alkynylation of Thiols with Ethynylbenziodoxolone (EBX) Reagents: α- or β- π-Addition?Fast and highly chemoselective alkynylation of thiols with hypervalent iodine reagents enabled through a low energy barrier concerted mechanism.Gold-catalyzed direct alkynylation of tryptophan in peptides using TIPS-EBX.One-pot, three-component arylalkynyl sulfone synthesis.Room temperature decarboxylative cyanation of carboxylic acids using photoredox catalysis and cyanobenziodoxolones: a divergent mechanism compared to alkynylation.One-pot gold-catalyzed synthesis of 3-silylethynyl indoles from unprotected o-alkynylanilinesPd-catalyzed intramolecular oxyalkynylation of alkenes with hypervalent iodine.Direct alkynylation of indole and pyrrole heterocycles.Synthesis of aminocyclobutanes by iron-catalyzed [2+2] cycloaddition.Convenient synthesis of alkylhydrazides by the cobalt-catalyzed hydrohydrazination reaction of olefins and azodicarboxylates.Dearomatization of electron poor six-membered N-heterocycles through [3 + 2] annulation with aminocyclopropanes.Gold-catalyzed domino cyclization-alkynylation reactions with EBX reagents: new insights into the reaction mechanism.Divergent Reactivity of Thioalkynes in Lewis Acid Catalyzed Annulations with Donor-Acceptor Cyclopropanes.Indole- and Pyrrole-BX: Bench-Stable Hypervalent Iodine Reagents for Heterocycle Umpolung.Enantioselective Copper-Catalyzed Oxy-Alkynylation of Diazo Compounds.Heterotetracenes: Flexible Synthesis and in Silico Assessment of the Hole-Transport Properties.Divergent Access to (1,1) and (1,2)-Azidolactones from Alkenes using Hypervalent Iodine Reagents.One-Pot Three-Component Synthesis of Vicinal Diamines via In Situ Aminal Formation and Carboamination.Copper-Catalyzed Oxy-Alkynylation of Diazo Compounds with Hypervalent Iodine Reagents.Enantioselective synthesis of polycyclic carbocycles via an alkynylation-allylation-cyclization strategy.Iridium- and Rhodium-Catalyzed Directed C-H Heteroarylation of Benzaldehydes with Benziodoxolone Hypervalent Iodine Reagents.Lewis Acid Catalyzed Enantioselective Desymmetrization of Donor-Acceptor meso-Diaminocyclopropanes.Room temperature alkynylation of H-phosphi(na)tes and secondary phosphine oxides with ethynylbenziodoxolone (EBX) reagents.Palladium-Catalyzed Carboamination of Allylic Alcohols Using a Trifluoroacetaldehyde-Derived Tether.Platinum-catalyzed domino reaction with benziodoxole reagents for accessing benzene-alkynylated indoles.Proteome-Wide Profiling of Targets of Cysteine reactive Small Molecules by Using Ethynyl Benziodoxolone Reagents.Rhodium-catalyzed C-H functionalization of heteroarenes using indoleBX hypervalent iodine reagents.Fine-tuned organic photoredox catalysts for fragmentation-alkynylation cascades of cyclic oxime ethersStereoselective synthesis of alkyl-, aryl-, vinyl- and alkynyl-substituted -enamides and enol ethersGeneral and Practical Formation of Thiocyanates from Thiols
P50
Q29012012-897ABDF2-96F8-4FAD-A795-E2C10CB97AB8Q33459342-9B7B706A-6349-4A67-A137-10EB665C71DCQ34710815-DA716359-0745-4A52-B5DB-A1A1C5A5BC19Q35194222-A47E0FAE-B91B-4736-901A-219BA4B2D397Q37638450-DF636105-D220-4B26-B7FC-B3DC1BC192D4Q37785764-5CA958F9-D650-42EC-BCEF-23F6CA03ED48Q38735030-276F9A35-3408-4CF7-AE02-5040CA68700BQ39078264-14673CEF-1C79-41B6-ABEE-6436F5AE7450Q39695441-CAC8B3AC-8D37-490B-B080-2E0F64E3ED81Q41893328-D09CE40E-6A0F-4932-93DB-F77E7065C5E6Q41893377-004D0BCD-DFB3-44B1-9DAD-CDF29B9D17B7Q42134049-9502017D-F980-4706-A9A7-AB4C53BA7D33Q42172529-892BC08C-878D-42F1-A352-ADDBE90110AAQ42209490-536561BB-E7FA-4326-8B33-095B7FA7977BQ42291057-6A5C1C36-4A6A-4D1C-ADF4-FD526C599040Q42745426-4452AA86-8A5E-4357-B469-26B9315FE36DQ43226228-4E18BADA-DB70-4816-8AE9-E7425B313F49Q43247308-42B4B4AD-A8DF-41AB-BC91-977476F3182BQ44299429-EF76C4D7-EE33-4640-9B29-046D6463A2C9Q44882442-754FE8D4-4447-42C4-BEB6-CCF7C412BF0AQ47124388-7DC30C14-4510-4EE2-922E-7148B0B122D2Q48124221-3D3AB21E-8E94-4731-9278-E019902A74FBQ48154496-9EFE21B3-2547-4616-B91A-97001D35BAE9Q48259796-E4844379-B7A3-4B22-B5AB-75D523064107Q48267330-889C9B97-51ED-41A8-B1D9-DBC421C523D5Q48277177-0166AA77-509F-47E9-9AB9-91E91493587AQ48292370-5C557530-9A17-4C63-AF01-DF32BF50FF26Q48352455-49FE4A3A-180D-4C46-A1FA-6370D00B004EQ50881110-9BD4439D-DD27-429F-BEE5-CEDAFC174E0DQ51042766-8EA4E0D9-0FD9-4B57-9E10-B10AA323F196Q52375526-A201228A-55B5-4B5C-B3C2-1891823ABFCEQ52692990-A571B486-9F1A-4F8A-98D8-5556022E94E3Q52778915-76DBC148-D90E-4584-9B3F-B1BFF47A4A5FQ53227777-698EDBC1-6B55-4D9E-A38E-B2B50C385376Q53582886-323AC809-6709-43E3-89BB-D94F1EB73F5CQ53605842-F5DA61E4-079C-4160-B6AE-55D40B9E2369Q55447362-3563D5AA-6F79-461A-A8EF-888C569A43F7Q61926931-BD11C44D-F8B4-435C-8324-3AA3557CD4C3Q63973410-CFE4C899-2240-40F2-8E44-329EDC394BBCQ63973415-CAF06E09-A2DC-4204-A38C-B317B45A4084
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jerome Waser
@ast
Jerome Waser
@en
Jerome Waser
@es
Jerome Waser
@nl
Jerome Waser
@sl
type
label
Jerome Waser
@ast
Jerome Waser
@en
Jerome Waser
@es
Jerome Waser
@nl
Jerome Waser
@sl
prefLabel
Jerome Waser
@ast
Jerome Waser
@en
Jerome Waser
@es
Jerome Waser
@nl
Jerome Waser
@sl
P106
P21
P31
P496
0000-0002-4570-914X