Constraining an Irregular Peptide Secondary Structure through Ring-Closing Alkyne MetathesisIron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking ChampionTotal syntheses of amphidinolide T1, T3, T4, and T5Total synthesis of myxovirescin A1PtCl2-catalyzed rearrangement of methylenecyclopropanesRecent Advancements in the Reformatsky ReactionOlefin Metathesis and BeyondFormal ring-opening/cross-coupling reactions of 2-pyrones: iron-catalyzed entry into stereodefined dienyl carboxylates.Diverted total synthesis: preparation of a focused library of latrunculin analogues and evaluation of their actin-binding propertiesDiaminocarbene- and Fischer-carbene complexes of palladium and nickel by oxidative insertion: preparation, structure, and catalytic activity.Discovery of Mycobacterium tuberculosis protein tyrosine phosphatase A (MptpA) inhibitors based on natural products and a fragment-based approach.Latrunculin analogues with improved biological profiles by "diverted total synthesis": preparation, evaluation, and computational analysis.Total synthesis and evaluation of the actin-binding properties of microcarpalide and a focused library of analogues.Total syntheses of the phytotoxic lactones herbarumin I and II and a synthesis-based solution of the pinolidoxin puzzle.The leiodolide B puzzle.Total Synthesis, Stereochemical Revision, and Biological Reassessment of Mandelalide A: Chemical Mimicry of Intrafamily Relationships.Total syntheses of amphidinolides B1, B4, G1, H1 and structure revision of amphidinolide H2.Concise total synthesis of the potent translation and cell migration inhibitor lactimidomycin.Total syntheses and biological reassessment of lactimidomycin, isomigrastatin and congener glutarimide antibiotics.Chemistry and biology of roseophilin and the prodigiosin alkaloids: a survey of the last 2500 years.trans-Hydrogenation: application to a concise and scalable synthesis of brefeldin AAlkyne metathesis.Catalytic carbophilic activation: catalysis by platinum and gold pi acids.Structural analogs of tylophora alkaloids may not be functional analogs.Catalysis-based enantioselective total synthesis of the macrocyclic spermidine alkaloid isooncinotine.Gold and platinum catalysis--a convenient tool for generating molecular complexity.Rearrangement of a Transient Gold Vinylidene into Gold Carbenes.From understanding to prediction: gold- and platinum-based π-acid catalysis for target oriented synthesis.Stabilization of a Chiral Dirhodium Carbene by Encapsulation and a Discussion of the Stereochemical Implications.Formation of Ruthenium Carbenes by gem-Hydrogen Transfer to Internal Alkynes: Implications for Alkyne trans-Hydrogenation.Molecular editing and assessment of the cytotoxic properties of iejimalide and progeny.Gram-scale synthesis of iejimalide B.Preparation, modification, and evaluation of cruentaren A and analogues.Orthogonal ring-closing alkyne and olefin metathesis for the synthesis of small GTPase-targeting bicyclic peptides.Structures of Reactive Donor/Acceptor and Donor/Donor Rhodium Carbenes in the Solid State and Their Implications for Catalysis.Tylophorine Analogs Allosterically Regulates Heat Shock Cognate Protein 70 And Inhibits Hepatitis C Virus Replication.The First Crystal Structure of a Reactive Dirhodium Carbene Complex and a Versatile Method for the Preparation of Gold Carbenes by Rhodium-to-Gold Transmetalation.Gold- or Silver-Catalyzed Syntheses of Pyrones and Pyridine Derivatives: Mechanistic and Synthetic Aspects.Formation of ruthenium carbenes by gem-hydrogen transfer to internal alkynes: implications for alkyne trans-hydrogenation.Structure assignment, total synthesis, and antiviral evaluation of cycloviracin B1.
P50
Q27728007-BBF86A1E-5DBB-461A-83DB-D276C8D161BEQ28072632-E99F27DC-D47B-41B8-8087-3D1D247DB72BQ28190357-9300F430-975F-44CF-8C45-25254DE4E417Q28220786-EA089D6C-E5AC-474C-A998-57A29C1E5F86Q28239059-AA405DB3-47AA-4309-90A3-A12A0CAAFDCAQ29397951-99035EE4-5A17-4CEE-9C76-B547678583EDQ29999051-38B65ABC-279D-4CCB-8E91-90DB5B874E91Q30486419-5DED78E3-BB07-4D59-9DD6-39B902F1DD22Q30853677-51BF0004-D7C8-4F51-9C9C-435E3A1EFAA6Q31144230-BAC4F59D-C7B0-431F-A5D0-337E13B50A68Q33224289-FBEA22B9-2004-4B6F-9ADD-D5A98FCEAC0DQ33262990-353560EB-D988-4F63-8006-800AD7E36210Q33264529-32569F2A-1CBA-4665-8540-247301F42885Q33337298-02A34193-2A83-47FA-A613-EC3C9970BF3EQ33350120-6383670D-58E1-43DF-9958-4E4EE5EB77D7Q33360970-9DFA862A-2BAA-4D71-9D1A-0600F63340ADQ33412219-1F3BC146-FBC3-4D1D-A8CA-DBC9506F45CAQ34137225-38A3FE89-6B72-4504-A847-D69273F1151DQ34339977-40FA0550-E608-4EBA-A67A-7995248B338BQ35198509-D71386DC-8E7A-42EF-8BEE-F6EC5CC0678DQ35753720-7519B583-0F41-4760-8D9E-077D39B619E7Q36118263-BE35C318-E3C1-40CA-92FD-F7D726960C5CQ36788319-22C52650-9174-4DDE-857A-64A49D08853AQ37240476-E769D538-173F-44FB-9E23-9AED5A1D89D8Q37484172-4A81994B-0065-4631-A522-C4B11B27D66EQ37619277-E39D4C16-89D1-4D32-9163-8815DC3710E9Q38946542-2717D149-4CA3-4100-8234-E5AE0E10C7D7Q39307175-40522DFD-9976-4D5D-859D-60C30E1467ABQ39532227-13FF778A-426A-4558-A1FE-D2E2E1BA9FDCQ39539281-54241108-D0F9-41A1-8E0E-803FC21253C3Q39545285-6DBC9199-911B-4E11-8B99-DE21ACFC0AFEQ39545292-8CD1934A-61C6-4A88-B2F6-960AF6AABE2FQ39788640-D2EB49CC-6AC6-47A3-AA83-0050625E3057Q39852763-259A4539-63B6-442D-B3D8-8ACA853FE87CQ39972139-93BCFB18-1333-40A6-BC39-5AAA91004875Q40064226-961DA563-D200-4FDC-BCDA-5982097FBFF4Q40214086-C4A63B00-1A53-431B-A435-82DEB94FF853Q40289857-D2835079-04DC-408B-95FD-A584048B7FB1Q40581797-07DE3971-F324-4D2B-A63F-1EBA4738D218Q40624464-F2CA3805-9D6B-4769-8998-68AD936FBD18
P50
description
Austria keemik
@et
Austrian chemist
@en
Austrian chemist
@en-ca
Austrian chemist
@en-gb
austerriksk kjemikar
@nn
aŭstra kemiisto
@eo
ceimiceoir Ostarach
@ga
chimist austriac
@ro
chimiste autrichien
@fr
cimiciste osteraices
@lfn
name
Alois Fürstner
@ast
Alois Fürstner
@ca
Alois Fürstner
@da
Alois Fürstner
@de
Alois Fürstner
@en
Alois Fürstner
@es
Alois Fürstner
@fr
Alois Fürstner
@ga
Alois Fürstner
@nb
Alois Fürstner
@nl
type
label
Alois Fürstner
@ast
Alois Fürstner
@ca
Alois Fürstner
@da
Alois Fürstner
@de
Alois Fürstner
@en
Alois Fürstner
@es
Alois Fürstner
@fr
Alois Fürstner
@ga
Alois Fürstner
@nb
Alois Fürstner
@nl
prefLabel
Alois Fürstner
@ast
Alois Fürstner
@ca
Alois Fürstner
@da
Alois Fürstner
@de
Alois Fürstner
@en
Alois Fürstner
@es
Alois Fürstner
@fr
Alois Fürstner
@ga
Alois Fürstner
@nb
Alois Fürstner
@nl
P166
P214
P227
P244
P108
P166
P21
P213
0000 0001 1666 7270
P214
P227
P2381
P244
P27
P31
P512
P569
1962-07-23T00:00:00Z
P691
mub2015862703
P735
P7859
lccn-n95100618