Research graph
References from Glycopeptide Assembly <i>via</i> Selective Manganese(I)-Catalyzed C–H Alkenylations in Organic Media and in Water. Local targets link to admitted publications; unresolved targets remain external evidence.
Biological roles of oligosaccharides: all of the theories are correct
10.1093/glycob/3.2.97 · 1993 · External reference
Glycobiology: Toward Understanding the Function of Sugars
10.1021/cr940283b · 1996 · External reference
Paradigms for glycan-binding receptors in cell adhesion
10.1016/j.ceb.2007.09.004 · 2007 · External reference
Simply better glycoproteins
10.1038/nbt.2893 · 2014 · External reference
A Review of Cell Adhesion Studies for Biomedical and Biological Applications
10.3390/ijms160818149 · 2015 · External reference
Chemical glycobiology
10.1126/science.1059820 · 2001 · External reference
Processing of glycans on glycoprotein and glycopeptide antigens in antigen-presenting cells
10.1073/pnas.152345899 · 2002 · External reference
Glycosylation in health and disease
10.1038/s41581-019-0129-4 · 2019 · External reference
Glycomedicine: The Current State of the Art
10.1016/j.eng.2022.03.009 · 2023 · External reference
Method development of glycoprotein biomarkers for cancers
10.4155/bio-2017-0077 · 2017 · External reference
Viral glycoproteins: biological role and application in diagnosis
10.1007/s13337-015-0293-5 · 2016 · External reference
Nonpeptidal Peptidomimetics with a Beta-D-Glucose Scaffolding - a Partial Somatostatin Agonist Bearing a Close Structural Relationship to a Potent, Selective Substance-P Antagonist
10.1021/ja00049a081 · 1992 · External reference
Design, Synthesis, and Binding-Affinity of a Nonpeptide Mimic of Somatostatin
10.1016/s0960-894x(01)80435-2 · 1992 · External reference
Preparation of acylated compounds useful for the treatment of metabolic disorders and nonalcoholic fatty liver disease
2019 · External reference
Structure-based discovery of glycomimetic FmlH ligands as inhibitors of bacterial adhesion during urinary tract infection
10.1073/pnas.1720140115 · 2018 · External reference
Synthesis of aryl-thioglycopeptides through chemoselective Pd-mediated conjugation
10.1039/c8sc02370k · 2018 · External reference
Glycoprotein synthesis: an update
10.1021/cr078291i · 2009 · External reference
Glycopeptide and glycoprotein synthesis involving unprotected carbohydrate building blocks
10.1002/med.20033 · 2005 · External reference
Synthesis of Glycopeptides Containing Carbohydrate and Peptide Recognition Motifs
10.1021/cr990308c · 2000 · External reference
Transient Directing Groups for Transformative C–H Activation by Synergistic Metal Catalysis
10.1016/j.chempr.2017.11.002 · 2018 · External reference
C-H bond activation enables the rapid construction and late-stage diversification of functional molecules
10.1038/nchem.1607 · 2013 · External reference
Innate and guided C-H functionalization logic
10.1021/ar200194b · 2012 · External reference
Postsynthetic Modification of Peptides: Chemoselective C-Arylation of Tryptophan Residues
10.1002/chem.200902676 · 2010 · External reference
Synthesis of C-2 Arylated Tryptophan Amino Acids and Related Compounds through Palladium-Catalyzed C–H Activation
10.1021/jo400961x · 2013 · External reference
New peptide architectures through C-H activation stapling between tryptophan-phenylalanine/tyrosine residues
10.1038/ncomms8160 · 2015 · External reference
Constrained Cyclopeptides: Biaryl Formation through Pd-Catalyzed C–H Activation in Peptides—Structural Control of the Cyclization vs Cyclodimerization Outcome
10.1002/chem.201601832 · 2016 · External reference
Novel Acetoxylation and C–C Coupling Reactions at Unactivated Positions in α-Amino Acid Derivatives
10.1021/ol061389j · 2006 · External reference
Palladium-catalyzed trifluoroacetate-promoted mono-arylation of the β-methyl group of alanine at room temperature: synthesis of β-arylated α-amino acids through sequential C–H functionalization
10.1039/c4sc01545b · 2014 · External reference
Total synthesis of celogentin C by stereoselective C-H activation
10.1002/anie.200905134 · 2010 · External reference
Stereoselective synthesis of beta-alkylated alpha-amino acids via palladium-catalyzed alkylation of unactivated methylene C(sp3)-H bonds with primary alkyl halides
10.1021/ja406484v · 2013 · External reference
Palladium-catalyzed stereoretentive olefination of unactivated C(sp3)-H bonds with vinyl iodides at room temperature: synthesis of beta-vinyl alpha-amino acids
10.1021/ol503248f · 2014 · External reference
Syntheses and Transformations of α-Amino Acids via Palladium-Catalyzed Auxiliary-Directed sp3 C–H Functionalization
10.1021/acs.accounts.6b00022 · 2016 · External reference
A general strategy for synthesis of cyclophane-braced peptide macrocycles via palladium-catalysed intramolecular sp3 C–H arylation
10.1038/s41557-018-0006-y · 2018 · External reference
Nonnatural Amino Acid Synthesis by Using Carbon–Hydrogen Bond Functionalization Methodology
10.1002/anie.201200731 · 2012 · External reference
Bidentate, Monoanionic Auxiliary-Directed Functionalization of Carbon–Hydrogen Bonds
10.1021/ar5004626 · 2015 · External reference
Stereoselective Synthesis of Chiral β-Fluoro α-Amino Acids via Pd(II)-Catalyzed Fluorination of Unactivated Methylene C(sp3)–H Bonds: Scope and Mechanistic Studies
10.1021/jacs.5b03989 · 2015 · External reference
Divergent and Stereoselective Synthesis of β-Silyl-α-Amino Acids through Palladium-Catalyzed Intermolecular Silylation of Unactivated Primary and Secondary C–H Bonds
10.1002/anie.201607766 · 2016 · External reference
Site-Selective Alkenylation of δ-C(sp3)–H Bonds with Alkynes via a Six-Membered Palladacycle
10.1021/jacs.6b05978 · 2016 · External reference
Site-Selective δ-C(sp3)–H Alkylation of Amino Acids and Peptides with Maleimides via a Six-Membered Palladacycle
10.1002/anie.201801445 · 2018 · External reference
Divergent Synthesis of Silicon-Containing Peptides via Pd-Catalyzed Post-Assembly γ-C(sp3)–H Silylation
10.1021/acscatal.9b00544 · 2019 · External reference
Manganese(I)-Catalyzed C–H Allylation of Tryptophans and Their Oligopeptides On Water
10.1055/a-2268-4678 · 2024 · External reference
Late-stage C-H Functionalization of Tryptophan-Containing Peptides with Thianthrenium Salts: Conjugation and Ligation
10.1002/anie.202216661 · 2023 · External reference
Late-stage diversification of peptides by metal-free C-H arylation
10.1002/chem.201404603 · 2014 · External reference
Late-Stage Peptide Diversification by Bioorthogonal Catalytic C-H Arylation at 23 degrees in H2O
10.1002/chem.201501831 · 2015 · External reference
Manganese(I)-Catalyzed Dispersion-Enabled C-H/C-C Activation
10.1002/chem.201701191 · 2017 · External reference
Manganese-Catalyzed C-H Alkynylation: Expedient Peptide Synthesis and Modification
10.1002/anie.201611118 · 2017 · External reference
Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)-Catalyzed C-H Activation
10.1002/anie.201609631 · 2017 · External reference
Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp3)-H Activation
10.1002/anie.201710136 · 2018 · External reference
BODIPY Peptide Labeling by Late-Stage C(sp3)-H Activation
10.1002/anie.201804654 · 2018 · External reference
Late-Stage Diversification through Manganese-Catalyzed C-H Activation: Access to Acyclic, Hybrid, and Stapled Peptides
10.1002/anie.201812705 · 2019 · External reference
Late-Stage Peptide Diversification through Cobalt-Catalyzed C-H Activation: Sequential Multicatalysis for Stapled Peptides
10.1002/anie.201811668 · 2019 · External reference
Site-Selective C(sp3)–H Functionalization of Di-, Tri-, and Tetrapeptides at the N-Terminus
10.1021/ja510233h · 2014 · External reference
Ligand-controlled C(sp3)-H arylation and olefination in synthesis of unnatural chiral alpha-amino acids
10.1126/science.1249198 · 2014 · External reference
Regio- and Stereospecific Synthesis of C-3 Functionalized Proline Derivatives by Palladium Catalyzed Directed C(sp3)–H Arylation
10.1021/ol502511g · 2014 · External reference
Stereoselective Peptide Modifications via β-C(sp3)-H Arylations
10.1021/acs.joc.6b01963 · 2016 · External reference
Mild and Regioselective Pd(OAc)2-Catalyzed C–H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
10.1021/acscatal.6b03121 · 2017 · External reference
Pd-Catalyzed Dimethylation of Tyrosine-Derived Picolinamide for Synthesis of (S)-N-Boc-2,6-dimethyltyrosine and Its Analogues
10.1021/acs.orglett.6b03548 · 2017 · External reference
Backbone-Enabled Directional Peptide Macrocyclization through Late-Stage Palladium-Catalyzed δ-C(sp2)–H Olefination
10.1002/anie.201807953 · 2018 · External reference
Late-stage stitching enabled by manganese-catalyzed C─H activation: Peptide ligation and access to cyclopeptides
10.1126/sciadv.abe6202 · 2021 · External reference
Late-stage peptide labeling with near-infrared fluorogenic nitrobenzodiazoles by manganese-catalyzed C–H activation
10.1039/d3sc01868g · 2023 · External reference
Fluorescent coumarin-alkynes for labeling of amino acids and peptides via manganese(I)-catalyzed C–H alkenylation
10.1039/d4cc00361f · 2024 · External reference
Chemodivergent manganese-catalyzed C–H activation: modular synthesis of fluorogenic probes
10.1038/s41467-021-23462-9 · 2021 · External reference
Selective Labeling of Peptides with o-Carboranes via Manganese(I)-Catalyzed C–H Activation
10.1002/chem.202200811 · 2022 · External reference
Expanding GSK's solvent selection guide – embedding sustainability into solvent selection starting at medicinal chemistry
10.1039/c0gc00918k · 2011 · External reference
A survey of solvent selection guides
10.1039/c4gc01149j · 2014 · External reference
Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates
10.1055/s-0037-1610714 · 2019 · External reference
Sustainability as a Trigger for Innovation!
10.2533/chimia.2020.538 · 2020 · External reference
Water as the reaction medium in organic chemistry: from our worst enemy to our best friend
10.1039/d0sc06000c · 2021 · External reference
Organic synthesis in Aqueous Multiphase Systems — Challenges and opportunities ahead of us
10.1016/j.cocis.2021.101506 · 2021 · External reference
TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
10.1021/jo101974u · 2011 · External reference
"Designer"-Surfactant-Enabled Cross-Couplings in Water at Room Temperature
2012 · External reference
Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions
10.1038/s41596-019-0130-1 · 2019 · External reference
Phosphine Oxides as Preligands in Ruthenium-Catalyzed Arylations via C–H Bond Functionalization Using Aryl Chlorides
10.1021/ol051216e · 2005 · External reference
Ruthenium-Catalyzed Oxidative C–H Bond Alkenylations in Water: Expedient Synthesis of Annulated Lactones
10.1021/ol201563r · 2011 · External reference
[RhCp*Cl2]2-Catalyzed Directed N-Boc Amidation of Arenes “on Water”
10.1021/acs.orglett.5b00392 · 2015 · External reference
Ruthenium(II)-Catalyzed Microwave-Promoted Multiple C–H Activation in Synthesis of Hexa(heteroaryl)benzenes in Water
10.1021/acs.orglett.8b02169 · 2018 · External reference
Rhodium(III)-Catalyzed C–H Functionalization in Water for Isoindolin-1-one Synthesis
10.1021/acs.orglett.8b00780 · 2018 · External reference
Ruthenium(II)-Catalyzed C–H Bond [3+2] Annulation of N-Nitrosoanilines with Alkynes in Water
10.1002/ajoc.201900553 · 2019 · External reference
Water-mediated C–H activation of arenes with secure carbene precursors: the reaction and its application
10.1039/c9cc05804d · 2019 · External reference
Rhodium(III) catalyzed olefination and deuteration of tetrahydrocarbazole
10.1039/d1ra00236h · 2021 · External reference
A Water-Soluble Rhenium(I) Catalyst for the Regio- and Stereoselective C(sp2)–H Alkenylation of N-Pyridyl-/N-Pyrimidylindole and the N–H Alkenylation of N-Pyrimidylaniline Derivatives with Ynamides
10.1021/acs.orglett.0c04068 · 2021 · External reference
Green strategies for transition metal-catalyzed C–H activation in molecular syntheses
10.1039/d1qo00727k · 2021 · External reference
Recent Advances in Pd-Catalyzed Reactions Involving the “On-Water” Mechanism†
10.1002/cjoc.202300489 · 2024 · External reference
Earth-abundant 3d transition metals on the rise in catalysis
10.3762/bjoc.18.8 · 2022 · External reference
Manganese(I)-Catalyzed C–H Aminocarbonylation of Heteroarenes
10.1002/anie.201507087 · 2015 · External reference
Manganese-Catalyzed Synthesis of cis-β-Amino Acid Esters through Organometallic C–H Activation of Ketimines
10.1002/anie.201411808 · 2015 · External reference
Sustainable Manganese-Catalyzed C–H Activation/Hydroarylation of Imines
10.1002/cctc.201800144 · 2018 · External reference
C-H Activation: Toward Sustainability and Applications
10.1021/acscentsci.0c01413 · 2021 · External reference
Micellar Catalysis as a Tool for C-H Bond Functionalization toward C-C Bond Formation
10.1021/acs.organomet.2c00309 · 2022 · External reference
Towards a sustainable tomorrow: advancing green practices in organic chemistry
10.1039/d4gc01826e · 2024 · External reference
Ruthenium(II)-Catalyzed C–H Bond [3+2] Annulation of N-Nitrosoanilines with Alkynes in Water
10.1002/ajoc.201900553 · ExternalCitation · doi-reference
Total synthesis of celogentin C by stereoselective C-H activation
10.1002/anie.200905134 · ExternalCitation · doi-reference
Nonnatural Amino Acid Synthesis by Using Carbon–Hydrogen Bond Functionalization Methodology
10.1002/anie.201200731 · ExternalCitation · doi-reference
Manganese-Catalyzed Synthesis of cis-β-Amino Acid Esters through Organometallic C–H Activation of Ketimines
10.1002/anie.201411808 · ExternalCitation · doi-reference
Manganese(I)-Catalyzed C–H Aminocarbonylation of Heteroarenes
10.1002/anie.201507087 · ExternalCitation · doi-reference
Divergent and Stereoselective Synthesis of β-Silyl-α-Amino Acids through Palladium-Catalyzed Intermolecular Silylation of Unactivated Primary and Secondary C–H Bonds
10.1002/anie.201607766 · ExternalCitation · doi-reference
Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)-Catalyzed C-H Activation
10.1002/anie.201609631 · ExternalCitation · doi-reference
Manganese-Catalyzed C-H Alkynylation: Expedient Peptide Synthesis and Modification
10.1002/anie.201611118 · ExternalCitation · doi-reference
Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp3)-H Activation
10.1002/anie.201710136 · ExternalCitation · doi-reference
Site-Selective δ-C(sp3)–H Alkylation of Amino Acids and Peptides with Maleimides via a Six-Membered Palladacycle
10.1002/anie.201801445 · ExternalCitation · doi-reference
BODIPY Peptide Labeling by Late-Stage C(sp3)-H Activation
10.1002/anie.201804654 · ExternalCitation · doi-reference
Backbone-Enabled Directional Peptide Macrocyclization through Late-Stage Palladium-Catalyzed δ-C(sp2)–H Olefination
10.1002/anie.201807953 · ExternalCitation · doi-reference
Late-Stage Peptide Diversification through Cobalt-Catalyzed C-H Activation: Sequential Multicatalysis for Stapled Peptides
10.1002/anie.201811668 · ExternalCitation · doi-reference
Late-Stage Diversification through Manganese-Catalyzed C-H Activation: Access to Acyclic, Hybrid, and Stapled Peptides
10.1002/anie.201812705 · ExternalCitation · doi-reference
Late-stage C-H Functionalization of Tryptophan-Containing Peptides with Thianthrenium Salts: Conjugation and Ligation
10.1002/anie.202216661 · ExternalCitation · doi-reference
Sustainable Manganese-Catalyzed C–H Activation/Hydroarylation of Imines
10.1002/cctc.201800144 · ExternalCitation · doi-reference
Postsynthetic Modification of Peptides: Chemoselective C-Arylation of Tryptophan Residues
10.1002/chem.200902676 · ExternalCitation · doi-reference
Late-stage diversification of peptides by metal-free C-H arylation
10.1002/chem.201404603 · ExternalCitation · doi-reference
Late-Stage Peptide Diversification by Bioorthogonal Catalytic C-H Arylation at 23 degrees in H2O
10.1002/chem.201501831 · ExternalCitation · doi-reference
Constrained Cyclopeptides: Biaryl Formation through Pd-Catalyzed C–H Activation in Peptides—Structural Control of the Cyclization vs Cyclodimerization Outcome
10.1002/chem.201601832 · ExternalCitation · doi-reference
Manganese(I)-Catalyzed Dispersion-Enabled C-H/C-C Activation
10.1002/chem.201701191 · ExternalCitation · doi-reference
Selective Labeling of Peptides with o-Carboranes via Manganese(I)-Catalyzed C–H Activation
10.1002/chem.202200811 · ExternalCitation · doi-reference
Recent Advances in Pd-Catalyzed Reactions Involving the “On-Water” Mechanism†
10.1002/cjoc.202300489 · ExternalCitation · doi-reference
Glycopeptide and glycoprotein synthesis involving unprotected carbohydrate building blocks
10.1002/med.20033 · ExternalCitation · doi-reference
Viral glycoproteins: biological role and application in diagnosis
10.1007/s13337-015-0293-5 · ExternalCitation · doi-reference
Paradigms for glycan-binding receptors in cell adhesion
10.1016/j.ceb.2007.09.004 · ExternalCitation · doi-reference
Transient Directing Groups for Transformative C–H Activation by Synergistic Metal Catalysis
10.1016/j.chempr.2017.11.002 · ExternalCitation · doi-reference
Organic synthesis in Aqueous Multiphase Systems — Challenges and opportunities ahead of us
10.1016/j.cocis.2021.101506 · ExternalCitation · doi-reference
Glycomedicine: The Current State of the Art
10.1016/j.eng.2022.03.009 · ExternalCitation · doi-reference
Design, Synthesis, and Binding-Affinity of a Nonpeptide Mimic of Somatostatin
10.1016/s0960-894x(01)80435-2 · ExternalCitation · doi-reference
Syntheses and Transformations of α-Amino Acids via Palladium-Catalyzed Auxiliary-Directed sp3 C–H Functionalization
10.1021/acs.accounts.6b00022 · ExternalCitation · doi-reference
Stereoselective Peptide Modifications via β-C(sp3)-H Arylations
10.1021/acs.joc.6b01963 · ExternalCitation · doi-reference
Micellar Catalysis as a Tool for C-H Bond Functionalization toward C-C Bond Formation
10.1021/acs.organomet.2c00309 · ExternalCitation · doi-reference
A Water-Soluble Rhenium(I) Catalyst for the Regio- and Stereoselective C(sp2)–H Alkenylation of N-Pyridyl-/N-Pyrimidylindole and the N–H Alkenylation of N-Pyrimidylaniline Derivatives with Ynamides
10.1021/acs.orglett.0c04068 · ExternalCitation · doi-reference
[RhCp*Cl2]2-Catalyzed Directed N-Boc Amidation of Arenes “on Water”
10.1021/acs.orglett.5b00392 · ExternalCitation · doi-reference
Pd-Catalyzed Dimethylation of Tyrosine-Derived Picolinamide for Synthesis of (S)-N-Boc-2,6-dimethyltyrosine and Its Analogues
10.1021/acs.orglett.6b03548 · ExternalCitation · doi-reference
Rhodium(III)-Catalyzed C–H Functionalization in Water for Isoindolin-1-one Synthesis
10.1021/acs.orglett.8b00780 · ExternalCitation · doi-reference
Ruthenium(II)-Catalyzed Microwave-Promoted Multiple C–H Activation in Synthesis of Hexa(heteroaryl)benzenes in Water
10.1021/acs.orglett.8b02169 · ExternalCitation · doi-reference
Mild and Regioselective Pd(OAc)2-Catalyzed C–H Arylation of Tryptophans by [ArN2]X, Promoted by Tosic Acid
10.1021/acscatal.6b03121 · ExternalCitation · doi-reference
Divergent Synthesis of Silicon-Containing Peptides via Pd-Catalyzed Post-Assembly γ-C(sp3)–H Silylation
10.1021/acscatal.9b00544 · ExternalCitation · doi-reference
C-H Activation: Toward Sustainability and Applications
10.1021/acscentsci.0c01413 · ExternalCitation · doi-reference
Innate and guided C-H functionalization logic
10.1021/ar200194b · ExternalCitation · doi-reference
Bidentate, Monoanionic Auxiliary-Directed Functionalization of Carbon–Hydrogen Bonds
10.1021/ar5004626 · ExternalCitation · doi-reference
Glycoprotein synthesis: an update
10.1021/cr078291i · ExternalCitation · doi-reference
Glycobiology: Toward Understanding the Function of Sugars
10.1021/cr940283b · ExternalCitation · doi-reference
Synthesis of Glycopeptides Containing Carbohydrate and Peptide Recognition Motifs
10.1021/cr990308c · ExternalCitation · doi-reference
Nonpeptidal Peptidomimetics with a Beta-D-Glucose Scaffolding - a Partial Somatostatin Agonist Bearing a Close Structural Relationship to a Potent, Selective Substance-P Antagonist
10.1021/ja00049a081 · ExternalCitation · doi-reference
Stereoselective synthesis of beta-alkylated alpha-amino acids via palladium-catalyzed alkylation of unactivated methylene C(sp3)-H bonds with primary alkyl halides
10.1021/ja406484v · ExternalCitation · doi-reference
Site-Selective C(sp3)–H Functionalization of Di-, Tri-, and Tetrapeptides at the N-Terminus
10.1021/ja510233h · ExternalCitation · doi-reference
Stereoselective Synthesis of Chiral β-Fluoro α-Amino Acids via Pd(II)-Catalyzed Fluorination of Unactivated Methylene C(sp3)–H Bonds: Scope and Mechanistic Studies
10.1021/jacs.5b03989 · ExternalCitation · doi-reference
Site-Selective Alkenylation of δ-C(sp3)–H Bonds with Alkynes via a Six-Membered Palladacycle
10.1021/jacs.6b05978 · ExternalCitation · doi-reference
TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
10.1021/jo101974u · ExternalCitation · doi-reference
Synthesis of C-2 Arylated Tryptophan Amino Acids and Related Compounds through Palladium-Catalyzed C–H Activation
10.1021/jo400961x · ExternalCitation · doi-reference
Phosphine Oxides as Preligands in Ruthenium-Catalyzed Arylations via C–H Bond Functionalization Using Aryl Chlorides
10.1021/ol051216e · ExternalCitation · doi-reference
Novel Acetoxylation and C–C Coupling Reactions at Unactivated Positions in α-Amino Acid Derivatives
10.1021/ol061389j · ExternalCitation · doi-reference
Ruthenium-Catalyzed Oxidative C–H Bond Alkenylations in Water: Expedient Synthesis of Annulated Lactones
10.1021/ol201563r · ExternalCitation · doi-reference
Regio- and Stereospecific Synthesis of C-3 Functionalized Proline Derivatives by Palladium Catalyzed Directed C(sp3)–H Arylation
10.1021/ol502511g · ExternalCitation · doi-reference
Palladium-catalyzed stereoretentive olefination of unactivated C(sp3)-H bonds with vinyl iodides at room temperature: synthesis of beta-vinyl alpha-amino acids
10.1021/ol503248f · ExternalCitation · doi-reference
Simply better glycoproteins
10.1038/nbt.2893 · ExternalCitation · doi-reference
C-H bond activation enables the rapid construction and late-stage diversification of functional molecules
10.1038/nchem.1607 · ExternalCitation · doi-reference
New peptide architectures through C-H activation stapling between tryptophan-phenylalanine/tyrosine residues
10.1038/ncomms8160 · ExternalCitation · doi-reference
Chemodivergent manganese-catalyzed C–H activation: modular synthesis of fluorogenic probes
10.1038/s41467-021-23462-9 · ExternalCitation · doi-reference
A general strategy for synthesis of cyclophane-braced peptide macrocycles via palladium-catalysed intramolecular sp3 C–H arylation
10.1038/s41557-018-0006-y · ExternalCitation · doi-reference
Glycosylation in health and disease
10.1038/s41581-019-0129-4 · ExternalCitation · doi-reference
Synthetic chemistry in water: applications to peptide synthesis and nitro-group reductions
10.1038/s41596-019-0130-1 · ExternalCitation · doi-reference
Expanding GSK's solvent selection guide – embedding sustainability into solvent selection starting at medicinal chemistry
10.1039/c0gc00918k · ExternalCitation · doi-reference
A survey of solvent selection guides
10.1039/c4gc01149j · ExternalCitation · doi-reference
Palladium-catalyzed trifluoroacetate-promoted mono-arylation of the β-methyl group of alanine at room temperature: synthesis of β-arylated α-amino acids through sequential C–H functionalization
10.1039/c4sc01545b · ExternalCitation · doi-reference
Synthesis of aryl-thioglycopeptides through chemoselective Pd-mediated conjugation
10.1039/c8sc02370k · ExternalCitation · doi-reference
Water-mediated C–H activation of arenes with secure carbene precursors: the reaction and its application
10.1039/c9cc05804d · ExternalCitation · doi-reference
Water as the reaction medium in organic chemistry: from our worst enemy to our best friend
10.1039/d0sc06000c · ExternalCitation · doi-reference
Green strategies for transition metal-catalyzed C–H activation in molecular syntheses
10.1039/d1qo00727k · ExternalCitation · doi-reference
Rhodium(III) catalyzed olefination and deuteration of tetrahydrocarbazole
10.1039/d1ra00236h · ExternalCitation · doi-reference
Late-stage peptide labeling with near-infrared fluorogenic nitrobenzodiazoles by manganese-catalyzed C–H activation
10.1039/d3sc01868g · ExternalCitation · doi-reference
Fluorescent coumarin-alkynes for labeling of amino acids and peptides via manganese(I)-catalyzed C–H alkenylation
10.1039/d4cc00361f · ExternalCitation · doi-reference
Towards a sustainable tomorrow: advancing green practices in organic chemistry
10.1039/d4gc01826e · ExternalCitation · doi-reference
Manganese(I)-Catalyzed C–H Allylation of Tryptophans and Their Oligopeptides On Water
10.1055/a-2268-4678 · ExternalCitation · doi-reference
Micelle-Mediated Chemistry in Water for the Synthesis of Drug Candidates
10.1055/s-0037-1610714 · ExternalCitation · doi-reference
Processing of glycans on glycoprotein and glycopeptide antigens in antigen-presenting cells
10.1073/pnas.152345899 · ExternalCitation · doi-reference
Structure-based discovery of glycomimetic FmlH ligands as inhibitors of bacterial adhesion during urinary tract infection
10.1073/pnas.1720140115 · ExternalCitation · doi-reference
Biological roles of oligosaccharides: all of the theories are correct
10.1093/glycob/3.2.97 · ExternalCitation · doi-reference
Late-stage stitching enabled by manganese-catalyzed C─H activation: Peptide ligation and access to cyclopeptides
10.1126/sciadv.abe6202 · ExternalCitation · doi-reference
Chemical glycobiology
10.1126/science.1059820 · ExternalCitation · doi-reference
Ligand-controlled C(sp3)-H arylation and olefination in synthesis of unnatural chiral alpha-amino acids
10.1126/science.1249198 · ExternalCitation · doi-reference
Sustainability as a Trigger for Innovation!
10.2533/chimia.2020.538 · ExternalCitation · doi-reference
A Review of Cell Adhesion Studies for Biomedical and Biological Applications
10.3390/ijms160818149 · ExternalCitation · doi-reference
Earth-abundant 3d transition metals on the rise in catalysis
10.3762/bjoc.18.8 · ExternalCitation · doi-reference
Method development of glycoprotein biomarkers for cancers
10.4155/bio-2017-0077 · ExternalCitation · doi-reference
