about
Π-Clamp-mediated cysteine conjugationChemo- and site-selective derivatizations of natural products enabling biological studies.Catalyst recognition of cis-1,2-diols enables site-selective functionalization of complex moleculesX-ray crystal structure of teicoplanin A₂-2 bound to a catalytic peptide sequence via the carrier protein strategy.Structure diversification of vancomycin through peptide-catalyzed, site-selective lipidation: a catalysis-based approach to combat glycopeptide-resistant pathogens.Site-Selective Acylations with Tailor-Made Catalysts.Catalytic site-selective thiocarbonylations and deoxygenations of vancomycin reveal hydroxyl-dependent conformational effects.Enhanced site-selectivity in acylation reactions with substrate-optimized catalysts on solid supports.A stepwise dechlorination/cross-coupling strategy to diversify the vancomycin 'in-chloride'.N-Methylimidazole-catalyzed synthesis of carbamates from hydroxamic acids via the Lossen rearrangementProbing the role of the vancomycin e-ring aryl chloride: selective divergent synthesis and evaluation of alternatively substituted E-ring analogues.Asymmetric catalysis at a distance: catalytic, site-selective phosphorylation of teicoplaninChemical tailoring of teicoplanin with site-selective reactionsLate Stage Azidation of Complex Molecules.Distal Stereocontrol Using Guanidinylated Peptides as Multifunctional Ligands: Desymmetrization of Diarylmethanes via Ullman Cross-Coupling.The generation of "unnatural" products: synthetic biology meets synthetic chemistry.Catalytic selective synthesis.Glycopeptide antibiotics: back to the future.Bluegenics: Bioactive Natural Products of Medicinal Relevance and Approaches to Their Diversification.Applications of Nonenzymatic Catalysts to the Alteration of Natural Products.Natural product analogues: towards a blueprint for analogue-focused synthesis.Catalytic promiscuity of glycopeptide N-methyltransferases enables bio-orthogonal labelling of biosynthetic intermediates.Late-stage deoxyfluorination of alcohols with PhenoFluor.Living GenoChemetics by hyphenating synthetic biology and synthetic chemistry in vivoBifunctional organocatalysts for the asymmetric synthesis of axially chiral benzamides.Regiodivergent Glycosylations of 6-Deoxy-erythronolide B and Oleandomycin-Derived Macrolactones Enabled by Chiral Acid Catalysis.Harnessing non-covalent interactions to exert control over regioselectivity and site-selectivity in catalytic reactions.Electronic tuning of site-selectivity.Palau'chlor: a practical and reactive chlorinating reagent.Practical silyl protection of ribonucleosides.A concise synthesis of L-pyrrolysine.Catalyst-Controlled Site-Selective Bond Activation.Reactions of hexadehydro-Diels-Alder benzynes with structurally complex multifunctional natural products.Developments in Glycopeptide Antibiotics.Desymmetrization of Diarylmethylamido Bis(phenols) through Peptide-Catalyzed Bromination: Enantiodivergence as a Consequence of a 2 amu Alteration at an Achiral Residue within the Catalyst.Site- and Stereoselective Chemical Editing of Thiostrepton by Rh-Catalyzed Conjugate Arylation: New Analogues and Collateral Enantioselective Synthesis of Amino Acids.Induction of Axial Chirality in 8-Arylquinolines through Halogenation Reactions Using Bifunctional Organocatalysts.A DNA-conjugated small molecule catalyst enzyme mimic for site-selective ester hydrolysis.
P2860
Q28833204-48B6BEFF-B1FA-4ECC-AA52-074B5E5F682EQ33699233-CD1E7DBB-6DDB-49D7-920C-0D8F81C61CE9Q33942260-FF42AA7D-7EC6-41CC-8DF2-F8D99073AF5EQ34211592-A0B51F13-3855-4D47-BD53-45A593EC97A8Q35190498-94237AF5-4C96-4A76-B24E-7DCF9B0D96D6Q35955106-AC6095F7-D6F5-4FBE-B118-3612E59457C6Q36030883-394E560B-88D3-4BF3-8E18-EE8D620C7F30Q36292635-0798FFBE-E586-4CC8-993A-D22B5BC2A7A1Q36505710-CE22AC7E-2BA6-4AEE-8A73-3E419127F650Q36583830-D5A4B293-680D-4E71-9386-0E678A9F6C89Q36886883-574364F3-A0F8-448C-85CF-D478172E4BE8Q37215640-C46C8BB5-7C97-47E7-964F-66C9674EAFBAQ37238862-EB0359E6-CBE2-440F-8FE2-27B72B71F00DQ37374082-2213322F-BADB-414F-8C4E-3D6C0BF65664Q37450559-6A288D00-5D2C-4CB0-8B0E-074362398C80Q38022529-A156343E-4752-4DE3-9D3E-E839472A63C2Q38046517-767D43B9-9533-4685-8B4C-2C9B88215FA2Q38239460-999F5B81-5AC9-4136-8FA4-F5ED24EA4F61Q39151177-8ADE8356-FDFC-45B3-BC3D-74F46160B761Q39350547-BF72F1AF-789B-4BCB-866E-971307F92B0FQ39413228-1BA7A1AC-9789-4D53-AD0E-C83DD43BC00FQ40464269-09718ECF-A49A-4D70-AA71-8438B2830CBFQ41154032-248236AB-C3B0-45C8-B99A-2F9D2BD0E923Q41331494-F6253973-B986-413F-B6F1-330293CE7CDEQ41334976-B4C85606-658E-4721-93BA-1EF99027FDE4Q41364493-B01765E9-8964-4D12-BD98-E354607FC8DDQ41787281-B7392AFA-9F8F-4E4C-8F4E-D9FB5C630516Q41856440-F9D9CC88-D3A8-4A1E-AFB6-79D3290946A4Q41901628-7BE7B3A9-C5B4-4CFA-9E0E-2A93C66B2A5CQ42829919-961A1908-4FC3-46E3-91D9-1C525AA4B107Q43453717-F4AEC99D-3385-47AC-A61E-7D12F00B2689Q46031469-5CD14778-57DA-4A25-809B-808E10CA894BQ46361623-2503EF25-F5B6-4E08-BD62-444A2CFDCCFFQ47715119-EA15E065-8FA5-4389-A1EB-C372FC3E1B4BQ48209249-DCC8850A-929A-4DCC-920D-BD6323743632Q48247643-1220DE45-EA68-4519-A340-EB426EE08F15Q48248888-1DA27647-91CB-4D3B-98D4-8EE4BC930A20Q55064385-DD4D19EB-0D4F-4F1C-AD09-843F6050A9C2
P2860
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Site-selective bromination of vancomycin.
@ast
Site-selective bromination of vancomycin.
@en
type
label
Site-selective bromination of vancomycin.
@ast
Site-selective bromination of vancomycin.
@en
prefLabel
Site-selective bromination of vancomycin.
@ast
Site-selective bromination of vancomycin.
@en
P2860
P356
P1476
Site-selective bromination of vancomycin
@en
P2093
Tejas P Pathak
P2860
P304
P356
10.1021/JA301566T
P407
P577
2012-03-30T00:00:00Z