New chemistry with old functional groups: on the reaction of isonitriles with carboxylic acids--a route to various amide types.
about
Encouraging progress in the ω-aspartylation of complex oligosaccharides as a general route to β-N-linked glycopolypeptides.Insights into the finer issues of native chemical ligation: an approach to cascade ligations.Discovery of competing anaerobic and aerobic pathways in umpolung amide synthesis allows for site-selective amide 18O-labeling.A fascinating journey into history: exploration of the world of isonitriles en route to complex amidesFully Synthetic Granulocyte Colony-Stimulating Factor Enabled by Isonitrile-Mediated Coupling of Large, Side-Chain-Unprotected PeptidesSynthesis of β-Glycosyl Amides from N-Glycosyl Dinitrobenzenesulfonamides.Addressing mechanistic issues in the coupling of isonitriles and carboxylic acids: potential routes to peptidic constructs.On the two-component microwave-mediated reaction of isonitriles with carboxylic acids: regarding alleged formimidate carboxylate mixed anhydrides.Noncatalytic reaction of isonitriles and carboxylic acids en route to amide-type linkagesSolid-phase peptide synthesis and solid-phase fragment coupling mediated by isonitrilesReaction of isonitriles with carboxylic acids in a cavitand: observation of elusive isoimide intermediatesChemistry and catalysis in functional cavitands.Toward homogeneous erythropoietin: chemical synthesis of the Ala1-Gly28 glycopeptide domain by "alanine" ligation.Recent Departures in the Synthesis of Peptides and Glycopeptides.Multicomponent Reactions, Union of MCRs and Beyond.Stabilization of reactive species by supramolecular encapsulation.Total synthesis of cyclosporine: access to N-methylated peptides via isonitrile coupling reactions.Silyl imine electrophiles in enantioselective catalysis: a Rosetta Stone for peptide homologation, enabling diverse N-protected aryl glycines from aldehydes in three steps.On the synthesis of conformationally modified peptides through isonitrile chemistry: implications for dealing with polypeptide aggregationUmpolung reactivity in amide and peptide synthesis.Thio-mediated two-component coupling reaction of carboxylic acids and isonitriles under mild conditions.Rhodium-catalyzed annulation of N-benzoylsulfonamide with isocyanide through C-H activation.Thio-mediated synthesis of derivatized N-linked glycopeptides using isonitrile chemistryRevisiting oxytocin through the medium of isonitriles.Enhancing the scope of the Diels-Alder reaction through isonitrile chemistry: emergence of a new class of acyl-activated dienophilesCoupling reactions of hindered isonitriles and hindered alkyl thioacids: Mechanistic studies.Reaction of thioacids with isocyanates and isothiocyanates: a convenient amide ligation process.Thio FCMA intermediates as strong acyl donors: a general solution to the formation of complex amide bondsExpanding the limits of isonitrile-mediated amidations: on the remarkable stereosubtleties of macrolactam formation from synthetic seco-cyclosporins.On the Preparation of Enantiomerically Pure Isonitriles from Amino Acid Esters and Peptides.Preparation and reactions of N-thioformyl peptides from amino thioacids and isonitriles.Three-component metal-free arylation of isocyanides.Synthesis of Peptides by Silver-Promoted Coupling of Carboxylates and Thioamides: Mechanistic Insight from Computational Studies.9-Silafluorenyl Dichlorides as Chemically Ligating Coupling Agents and Their Application in Peptide Synthesis.In situ generation of nitrilium from nitrile ylide and the subsequent Mumm rearrangement: copper-catalyzed synthesis of unsymmetrical diacylglycine esters.Direct acyl substitution of carboxylic acids: a chemoselective O- to N-acyl migration in the traceless Staudinger ligation.
P2860
Q34550860-CDCC255F-14EF-4DA2-A782-9DCBDD452DADQ35421347-F8E42F31-FCB0-49B4-924C-A215F761CA4EQ35657758-0621E511-D97B-4298-A69B-D269CE5CEAA0Q36131535-BA5F0024-30E2-43E6-BEE0-321B0DA33D24Q36198586-C5D240BA-3C82-477D-A471-4B30AB68BF5FQ36552041-AC069787-57AB-472E-9422-9C983CFB40DBQ36967304-DE773D6E-737C-4804-BEB5-F34C86955891Q36967314-ED4EF41C-1A39-4A41-A1F2-4106EDE8097AQ36982931-27CC418D-F720-4879-A803-A3949AFDC2BCQ37031771-DA9C02C0-38A3-4892-9143-0B9D8E016816Q37096626-E0F9E87A-4CD1-4ABE-978D-26E371B26509Q37142217-40FB2267-7D1B-43D5-B62C-A4710288CED3Q37395856-719157E9-D10D-437F-9CC0-1A787C0A3222Q37428099-684E303F-963F-4F75-B22D-EFC13CF98B76Q38603972-0B6FD2B0-F60D-489F-BF94-702387233193Q38707091-0F8CAAA4-479E-4A91-ABBF-FB1E80DBE880Q39781344-C6FDB8AA-ABF1-4A8B-9115-70625387C7C2Q40759490-2DB1C34C-28F2-47E6-9F45-B1D87AC92682Q41948467-A94410F8-1DF1-4976-B605-54DDB9573120Q41953928-5843554D-8186-4C52-9D60-EA03751B97A8Q41971552-DA4BFBE7-156F-47AB-8298-8D6202AB166FQ42042310-2AF5DA82-A20B-4D3E-A546-E0C8445F8E29Q42099444-67BC03EE-4938-4EDB-911E-5483EA749AA0Q42123499-4DE199BD-D6B2-459D-A65B-99EF24A1B68FQ42236917-F25BD88B-94C9-4C0D-BB02-3D77BA26C74DQ42254277-57765C3D-1CBC-4F6C-A215-BA27550269ECQ42548089-1FCAE6A8-9B7E-4D30-8E8D-37C010877560Q42576069-EBAE7CB5-8391-465F-808E-01C57F49DC80Q42577805-A8F7B072-4B02-44CE-AB1F-CB3CDD9BA6ADQ42873120-405EC420-A574-4685-85BB-581438C1BBD4Q43117983-7F87405C-35CB-4E8B-A990-22A137081295Q44806404-348664D5-06B0-42E9-A67C-ACBEB7291EE3Q48044465-704FA3C2-D5B7-4415-A75E-D72A26437517Q50217574-3A8527D0-329D-4BB7-A2D5-076C8F293DB4Q51112075-2A46DBBA-D284-4B3C-9C04-222D4384D554Q53755902-8E5A5B5F-E3A0-479A-92E1-41C62C932CDD
P2860
New chemistry with old functional groups: on the reaction of isonitriles with carboxylic acids--a route to various amide types.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
New chemistry with old functio ...... route to various amide types.
@en
type
label
New chemistry with old functio ...... route to various amide types.
@en
prefLabel
New chemistry with old functio ...... route to various amide types.
@en
P2860
P356
P1476
New chemistry with old functio ...... route to various amide types.
@en
P2093
Samuel J Danishefsky
Xuechen Li
P2860
P304
P356
10.1021/JA800612R
P407
P577
2008-03-28T00:00:00Z