about
A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagentsRecent extensions to native chemical ligation for the chemical synthesis of peptides and proteins.Site-selective solid-phase synthesis of a CCR5 sulfopeptide library to interrogate HIV binding and entry.Organic chemistry. Strain-release amination.Strain-Release Heteroatom Functionalization: Development, Scope, and Stereospecificity.Peptide ligation chemistry at selenol amino acids.Self-adjuvanting multicomponent cancer vaccine candidates combining per-glycosylated MUC1 glycopeptides and the Toll-like receptor 2 agonist Pam3CysSer.Oxidative Deselenization of Selenocysteine: Applications for Programmed Ligation at Serine.Peptide Macrocyclization Inspired by Non-Ribosomal Imine Natural Products.Decarboxylative alkenylation.Residue-Specific Peptide Modification: A Chemist's Guide.Peptide ligation-desulfurization chemistry at arginine.Nickel-Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms.Decarboxylative Alkynylation.Single addition of an allylamine monomer enables access to end-functionalized RAFT polymers for native chemical ligation.Peptide modification and cyclization via transition-metal catalysis.CITU: A Peptide and Decarboxylative Coupling Reagent.Modern extensions of native chemical ligation for chemical protein synthesis.One-Pot Ligation-Oxidative Deselenization at Selenocysteine and Selenocystine.One-pot peptide ligation-desulfurization at glutamate.Total Synthesis of SuillusinSynthesis and utility of β-selenol-phenylalanine for native chemical ligation-deselenization chemistrySynthesis of MUC1-lipopeptide chimerasThiazolidine-Protected β-Thiol Asparagine: Applications in One-Pot Ligation-Desulfurization ChemistryRapid additive-free selenocystine-selenoester peptide ligationSynthesis of β-Thiol Phenylalanine for Applications in One-Pot Ligation-Desulfurization ChemistryHitting the sweet spotLate-Stage Functionalization of Histidine in Unprotected PeptidesCorrigendum: Nickel-Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic TransformsStructurally Diverse Acyl Bicyclobutanes: Valuable Strained Electrophiles
P50
Q28834226-E055E45A-0002-4611-8A89-2F1B064365B9Q30367477-E08DF6F4-200C-4E72-8857-28728A722CE9Q35194597-453A8F48-E952-455C-9171-DC4EC3B9D47FQ36514239-BE66EB3D-0A5E-4671-91D4-BCD871F73FDCQ37678579-E01C8899-030B-424D-AB35-CB4E6E6F526FQ38166998-BD1C2F43-DFF6-4959-9EA0-2A2D6D217649Q39594793-873BEC1E-E062-44B1-8090-A817FB4110B8Q40524884-F7D4F19B-B9A2-46B0-9A26-18E75B536162Q42291656-8988B70E-1B10-4AE4-8362-557A685D3494Q42336176-62A5A263-574D-434A-A5C7-96029EC2AD28Q43905157-F4E298E0-E69E-477C-B042-B60E1D54E53EQ45217986-92AB9E46-B983-4FA8-9007-843BBBC9BCEDQ48146740-A7DC9EFE-5DAE-4B49-BFFA-908D06B48EB1Q48245463-5228360A-0590-44A9-8259-96025EF50707Q48272739-0F277394-EDAE-475C-BFE7-CD67164EE725Q52587994-4AA1AF2F-B331-483E-983E-9D32BE8523A0Q52803234-B1A1CDB7-01EE-4C1F-968E-E602D7EE3200Q53358774-5A2473F7-D080-4655-9119-C3474AD49AD1Q53551507-5235F9C8-C7D2-4C2B-AC12-9007E098609BQ54505600-A6C70E24-B4C1-4A51-990D-60D82A96A84DQ58090637-6B2ADB2C-AA33-49BA-A04D-D2E8E444F82EQ84238506-528160D4-F7AC-47CC-A7BF-94B094215CB5Q84602045-88CAECF2-41F0-4B0F-95F7-EA70B66790E0Q86230557-0A78C23D-131E-42C5-901E-781076F24AC8Q86526530-23499B22-1821-4BCF-8436-D0CDB6899045Q87090314-9A824CEB-A05B-45E6-B9FA-C275B871EEB8Q88764696-33AEFF77-BEBA-420B-B5F1-25DD05B9C4F9Q90690454-693C66D0-5932-4B7B-9B90-1A597EF7AB2FQ91327467-B66F020B-E7C0-441C-80D2-9479C3488F23Q91860402-118030F7-F286-4358-B17B-2761EAFB2671
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Lara R Malins
@ast
Lara R Malins
@en
Lara R Malins
@es
Lara R Malins
@nl
type
label
Lara R Malins
@ast
Lara R Malins
@en
Lara R Malins
@es
Lara R Malins
@nl
prefLabel
Lara R Malins
@ast
Lara R Malins
@en
Lara R Malins
@es
Lara R Malins
@nl
P106
P1153
56431365000
P31
P496
0000-0002-7691-6432