about
Practical formal total syntheses of the homocamptothecin derivative and anticancer agent diflomotecan via asymmetric acetate aldol additions to pyridine ketone substratesCooperative Al(salen)-pyridinium catalysts for the asymmetric synthesis of trans-configured β-lactones by [2+2]-cyclocondensation of acylbromides and aldehydes: investigation of pyridinium substituent effects.Unified total synthesis of pteriatoxins and their diastereomersCatalytic asymmetric synthesis of trans-configured beta-lactones: cooperation of Lewis acid and ion pair catalysis.Catalytic asymmetric formation of delta-lactones from unsaturated acyl halides.The asymmetric aza-Claisen rearrangement: development of widely applicable pentaphenylferrocenyl palladacycle catalysts.Catalytic asymmetric synthesis of spirocyclic azlactones by a double Michael-addition approach.Catalytic asymmetric synthesis of beta-sultams as precursors for taurine derivatives.An Aluminum Fluoride Complex with an Appended Ammonium Salt as an Exceptionally Active Cooperative Catalyst for the Asymmetric Carboxycyanation of Aldehydes.Synthesis of nearly enantiopure allylic amines by aza-Claisen rearrangement of Z-configured allylic trifluoroacetimidates catalyzed by highly active ferrocenylbispalladacycles.Practical formal total synthesis of (rac)- and (S)-camptothecin.Cooperative Lewis acid-onium salt catalysis as tool for the desymmetrization of meso-epoxides.Highly Enantioselective Ferrocenyl Palladacycle-Acetate Catalysed Arylation of Aldimines and Ketimines with Arylboroxines.Double Regioselective Asymmetric C-Allylation of Isoxazolinones: Iridium-Catalyzed N-Allylation Followed by an Aza-Cope Rearrangement.Diastereoselective synthesis, structure and reactivity studies of ferrocenyloxazoline gold(i) and gold(ii) complexes.Regioselective Pd-Catalyzed Synthesis of 2,3,6-Trisubstituted Pyridines from Isoxazolinones.Regioselective catalytic asymmetric C-alkylation of isoxazolinones by a base-free palladacycle-catalyzed direct 1,4-addition.Asymmetric palladium(II)-catalyzed cascade reaction giving quaternary amino succinimides by 1,4-addition and a Nef-type reaction.Intervalence of two planar chiral 2-methylferrocenyl groups over a diaurum bridgeAsymmetric Carboxycyanation of Aldehydes by Cooperative AlF-/Onium Salt Catalysts: from Cyanoformate to KCN as Cyanide SourceThe SAMP-/RAMP-hydrazone methodology in asymmetric synthesisHeterogenization of ferrocene palladacycle catalysts on ROMP-derived monolithic supports and application to a Michael additionEin Aluminium-Fluorid-Komplex mit gekoppelter Ammonium-Einheit als außergewöhnlich aktiver kooperativer Katalysator in der asymmetrischen Carboxycyanierung von AldehydenParamagnetic Palladacycles with PdIII Centers Are Highly Active Catalysts for Asymmetric Aza-Claisen RearrangementsRecovery of carbonyl compounds from N,N-dialkylhydrazonesMacrocyclic ferrocenyl-bisimidazoline palladacycle dimers as highly active and enantioselective catalysts for the aza-claisen rearrangement of Z-configured N-para-methoxyphenyl trifluoroacetimidatesEnantioselective bimetallic catalysis of Michael additions forming quaternary stereocentersCatalytic enantio- and diastereoselective formation of beta-sultones: ring-strained precursors for enantioenriched beta-hydroxysulfonyl derivativesPractical, highly active, and enantioselective ferrocenyl-imidazoline palladacycle catalysts (FIPs) for the aza-Claisen rearrangement of N-para-methoxyphenyl trifluoroacetimidatesTotal syntheses of the antibacterial natural product abyssomicin CCatalytic asymmetric formation of beta-sultamsCatalytic asymmetric formation of delta-lactones by [4+2] cycloaddition of zwitterionic dienolates generated from alpha,beta-unsaturated acid chloridesAsymmetric formation of allylic amines with N-substituted quaternary stereocenters by Pd(II)-catalyzed aza-Claisen rearrangementsPreparation and diastereoselective ortho-metalation of chiral ferrocenyl imidazolines: remarkable influence of LDA as metalation additiveContact ion pair directed Lewis acid catalysis: asymmetric synthesis of trans-configured beta-lactonesA highly strained planar-chiral platinacycle for catalytic activation of internal olefins in the Friedel-Crafts alkylation of indolesLewis acid/base catalyzed [2+2]-cycloaddition of sulfenes and aldehydes: a versatile entry to chiral sulfonyl and sulfinyl derivativesCatalyst versus substrate induced selectivity: kinetic resolution by palladacycle catalyzed allylic imidate rearrangementsBispalladacycle-catalyzed Brønsted acid/base-promoted asymmetric tandem azlactone formation-Michael additionExogenous-Base-Free Palladacycle-Catalyzed Highly Enantioselective Arylation of Imines with Arylboroxines
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Q28200522-06643BDB-922F-4776-8DC4-71E24E063D18Q34301693-B0E304AD-9C33-4D89-BE07-33CA3D650698Q36836843-5CC242A2-C65A-4491-ACEF-0A40E96DF061Q42985825-7FAA4D11-030A-49A8-8AD6-31601DEE8833Q43193407-9921382C-5BDA-46F3-9F6A-997158B85213Q43289823-B9588E31-74C4-440B-A167-F2FFFB81F563Q45680090-24B1F029-646A-48A6-9D3C-D4E438107328Q45927057-DA39F77D-B612-4CB0-AA45-546147D31792Q46411125-D95B810B-02AD-4E65-9944-BAA65BCF0643Q46837337-6CF90A9A-C588-4AF2-8598-C830C31ACC96Q46919413-EEF62018-EB55-4F34-AE02-ABAB0887B2B0Q48093976-BD3689B6-4B03-4A7A-A2AA-8C9004BC6750Q48145645-7D312726-2F60-4E72-ABDB-5158B42AC34FQ48283407-8C5F2012-1AC1-40AB-93CB-E0CCFAD95620Q49931752-C013A000-F8B5-4A08-87A1-230BC353F998Q50960815-1F508593-C61B-486E-B544-95D537DC40FEQ53655319-7FE6F248-2C56-4DCB-98BD-88DB9D5A9FC7Q54709732-4C626987-5C6A-467D-8673-5C4AB513B1A1Q56976600-107966C7-54E4-4ECF-AC70-31617B920CE8Q57785089-D3A5A05E-05EB-4A59-8B3A-83EB7B7E21A1Q59345492-317744E3-C8A4-4767-AE34-76F80A83ABB2Q59890589-93F6A38E-C2D3-448B-87BB-90EE5C1B3A2DQ59897634-15081881-99E0-47F5-BA19-8FA46E879B74Q64169669-3A900B6C-7CBF-4328-957E-5F02FF0ADCBBQ73570865-F5F5A563-4414-437E-B6AB-C736096C9186Q79522543-797EF024-B6B1-441F-B354-9B40CB102BA6Q79714179-60306431-2987-463F-8CE2-26EF7928648EQ79852224-3B120211-82C8-4816-A815-A855BD7526A4Q79956907-6BCB5B25-8D04-4908-ADFA-A5B8B375C953Q80103788-318BE4E4-43B5-4871-98A1-82523526D14EQ80190712-3A205C32-0E4E-4478-A832-5E64D27C2B63Q80414791-28E8372F-FCCA-4412-8017-8B1402A5D9CAQ80849436-4B06E943-EDFC-458E-9431-FA606681F7F4Q81175013-7A52006D-7300-4C98-B1DA-6A5293DBFA7DQ81416621-5A34CFAB-3C9E-4321-AB1B-EB584710A965Q82918356-3B5995BD-D8B8-4FF7-9E8A-6FD12D4C8FD0Q83510415-00CA2D12-01F6-4395-9E6D-777E03BFECC2Q84488130-D0B18E9F-E438-48DD-B21E-F530946358EFQ84751622-50677ADC-83E3-4FDB-8694-A9556B67ACE7Q85404374-1177F71F-BB34-4EB3-98DF-49869636ABC9
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description
hulumtues
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researcher
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ricercatore
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scheikundige
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taighdeoir
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հետազոտող
@hy
name
René Peters
@ast
René Peters
@de
René Peters
@en
René Peters
@es
René Peters
@nl
René Peters
@sl
type
label
René Peters
@ast
René Peters
@de
René Peters
@en
René Peters
@es
René Peters
@nl
René Peters
@sl
prefLabel
René Peters
@ast
René Peters
@de
René Peters
@en
René Peters
@es
René Peters
@nl
René Peters
@sl
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0000 0000 1635 4760
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nb2015006045
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0000-0002-6668-4017
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1971-01-01T00:00:00Z
2000-01-01T00:00:00Z
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lccn-nb2015006045