H. Kunz

发表

SELECTIVE ENZYMATIC REMOVAL OF PROTECTING FUNCTIONS - HEPTYL ESTERS AS CARBOXY PROTECTING GROUPS IN PEPTIDE SYNTHESIS

H. Waldmann, P. Braun, W. Vogt, 1990 .

Enzymatic cleavage of tert butyl esters thermitase catalyzed deprotection of peptides and o glycopeptides

P. Hermann, H. Kunz, M. Schultz, 1992 .

Chemoenzymatic synthesis of O-glycopeptides carrying the tumor associated TN-antigen structure.

H. Waldmann, P. Braun, H. Kunz, 1993, Bioorganic & medicinal chemistry.

Enzymatic hydrolysis of hydrophilic diethyleneglycol and polyethyleneglycol esters of peptides and glycopeptides by lipases

P. Braun, H. Kunz, D. Kowalczyk, 1994 .

Comparative Lipase-Catalyzed Hydrolysis of Ethylene Glycol Derived Esters. The 2-Methoxyethyl Ester as a Protective Group in Peptide and Glycopeptide Synthesis

H. Kunz, Markus Gewehr, 1997 .

Selective Enzymatic Removal of Protecting Functions: Heptyl Esters as Carboxy Protecting Groups in Glycopeptide Synthesis.

H. Waldmann, P. Braun, H. Kunz, 2010 .

Synthesis of Glycopeptides with Partial Structure of Human Glycophorin Using the Fluorenylmethoxycarbonyl/ Allyl Ester Protecting Group Combination

H. Kunz, Marita Ciommer, 1991 .

Synthesis of Tumor‐Associated Glycopeptide Antigens

H. Kunz, Constanze Brocke, 2002 .

A Synthetic MUC1 Anticancer Vaccine Containing Mannose Ligands for Targeting Macrophages and Dendritic Cells

E. Schmitt, H. Kunz, M. Glaffig, 2018, ChemMedChem.

Immunogenicity of a Fully Synthetic MUC1 Glycopeptide Antitumor Vaccine Enhanced by Poly(I:C) as a TLR3‐Activating Adjuvant

E. Schmitt, H. Kunz, M. Glaffig, 2017, ChemMedChem.

Immunization with a Synthetic Human MUC1 Glycopeptide Vaccine against Tumor‐Associated MUC1 Breaks Tolerance in Human MUC1 Transgenic Mice

E. Schmitt, H. Kunz, H. Jonuleit, 2017, ChemMedChem.

Enhanced immunogenicity of multivalent MUC1 glycopeptide antitumour vaccines based on hyperbranched polymers.

H. Frey, E. Schmitt, H. Kunz, 2015, Organic & biomolecular chemistry.

A new method of anomeric protection and activation based on the conversion of glycosyl azides into glycosyl fluorides.

H. Kunz, W. Bröder, 1993, Carbohydrate research.

The electronic substituent influence on the thermally allowed electrocyclic interconversion cyclobutene/butadiene. A MNDO study

H. Kunz, Axel Jensen, 1984 .

Diastereoselective Strecker Synthesis of α‐Aminonitriles on Carbohydrate Templates

H. Kunz, W. Sager, 1987 .

Carbohydrates as chiral templates: diastereoselective Ugi synthesis of (S)-amino acids using O-acylated D-arabinopyranosylamine as the auxiliary

H. Kunz, W. Sager, W. Pfrengle, 1989 .

Stereoselective synthesis of glycosides and anomeric azides of glucosamine

H. Kunz, C. Unverzagt, 1992 .

Combinatorial solid-phase synthesis using D-galactose as a chiral five-dimension-deversity scaffold

T. Opatz, H. Kunz, S. Henke, 1999 .

Evaluation of a novel monoclonal antibody against tumor-associated MUC1 for diagnosis and prognosis of breast cancer

Marcus Schmidt, M. Miederer, E. Schmitt, 2019, International journal of medical sciences.

Synthetic antitumor vaccines containing MUC1 glycopeptides with two immunodominant domains-induction of a strong immune response against breast tumor tissues.

H. Sinn, E. Schmitt, H. Kunz, 2011, Angewandte Chemie.

Fully synthetic vaccines consisting of tumor-associated MUC1 glycopeptides and a lipopeptide ligand of the Toll-like receptor 2.

E. Schmitt, Yan‐Mei Li, H. Kunz, 2010, Angewandte Chemie.

A synthetic vaccine consisting of a tumor-associated sialyl-T(N)-MUC1 tandem-repeat glycopeptide and tetanus toxoid: induction of a strong and highly selective immune response.

E. Schmitt, H. Kunz, D. Kowalczyk, 2009, Angewandte Chemie.

Synthetic vaccines consisting of tumor-associated MUC1 glycopeptide antigens and a T-cell epitope for the induction of a highly specific humoral immune response.

E. Schmitt, H. Kunz, Ulrika Westerlind, 2008, Angewandte Chemie.

Synthesis of glycopeptides and neoglycoproteins containing the fucosylated linkage region of N-glycoproteins.

H. Kunz, C. Unverzagt, 1994, Bioorganic & medicinal chemistry.

Protecting‐Group‐Dependent Stability of Intersaccharide Bonds—Synthesis of a Fucosyl‐Chitobiose Glycopeptide

H. Kunz, C. Unverzagt, 1988 .

Spacer-separated sialyl LewisX cyclopeptide conjugates as potential E-selectin ligands.

H. Kunz, H. Herzner, 2007, Carbohydrate research.

Highly regioselective synthesis of a 3-O-sulfonated arabino Lewis(a) asparagine building block suitable for glycopeptide synthesis.

H. Kunz, A. Rösch, 2006, Carbohydrate research.

Synthesis of glycopeptides with Lewis antigen or sialyl-Lewisx antigen side chains

H. Kunz, G. Kretzschmar, K. Bruch, 2002 .

Synthetic Inhibitors of Cell Adhesion: A Glycopeptide from E-Selectin Ligand 1 (ESL-1) with the Arabino Sialyl Lewisx Structure.

W. Dippold, D. Vestweber, H. Kunz, 2001, Angewandte Chemie.

Glycosyl azides as building blocks in convergent syntheses of oligomeric lactosamine and Lewis(x) saccharides.

H. Kunz, W. Bröder, 1997, Bioorganic & medicinal chemistry.

Developments in the synthesis of glycopeptides containing glycosyl L-asparagine, L-serine, and L-threonine.

H. Kunz, H. Garg, K. Bruch, 1994, Advances in carbohydrate chemistry and biochemistry.

Synthesis of N‐Glycopeptide Clusters with Lewisx Antigen Side Chains and Their Coupling to Carrier Proteins

H. Kunz, K. Bruch, 1994 .

[1] Neoglycoproteins from synthetic glycopeptides

H. Kunz, K. Bruch, 1994 .

Stereoselective Synthesis of Glycosides and Anomeric Azides of Glucosamine.

H. Kunz, C. Unverzagt, 1993 .

Glycoside and Saccharide Synthesis Using N-Glycosyl Triazoles as Hydrolytically Stable Glycosyl Donors

H. Kunz, W. Bröder, 1990 .

Synthesis of Glycopeptides, Partial Structures of Biological Recognition Components [New Synthetic Methods (67)]

H. Kunz, 1987 .

High-efficiency synthesis of sialyloligosaccharides and sialoglycopeptides

J. Paulson, H. Kunz, C. Unverzagt, 1990 .

Cyclodextrin-assisted Glycan Chain Extension on a Protected Glycosyl Amino Acid

A. Liese, H. Clausen, H. Kunz, 2000 .

Synthetic O-glycopeptides as model substrates for glycosyltransferases

H. Kunz, M. Schultz, 1993 .

HYCRON, an Allylic Anchor for High-Efficiency Solid Phase Synthesis of Protected Peptides and Glycopeptides

O. Seitz, H. Kunz, 1997 .

O‐Glycopeptide Synthesis using 9‐Fluorenylmethoxycarbonyl (Fmoc)‐Protected Synthetic Units

H. Kunz, P. Schultheiß‐Reimann, 1983 .

1,3-DITHIAN-2-YL METHYL-ESTER AS 2-STEP PROTECTING GROUP FOR THE CARBOXY FUNCTION IN PEPTIDE-SYNTHESIS

H. Waldmann, H. Kunz, 1983 .

Polymeric Selectin Ligands Mimicking Complex Carbohydrates: From Selectin Binders to Modifiers of Macrophage Migration.

F. Tacke, R. Zentel, E. Liehn, 2017, Angewandte Chemie.

A Synthetic Glycopeptide Vaccine for the Induction of a Monoclonal Antibody that Differentiates between Normal and Tumor Mammary Cells and Enables the Diagnosis of Human Pancreatic Cancer.

P. Flemming, E. Schmitt, H. Kunz, 2016, Angewandte Chemie.

Towards a fully synthetic MUC1-based anticancer vaccine: efficient conjugation of glycopeptides with mono-, di-, and tetravalent lipopeptides using click chemistry.

Yan‐Mei Li, Lei Shi, H. Kunz, 2011, Chemistry.

(p-Sulfomethyl)phenylalanine as a mimic of O-sulfatyl-tyrosine in synthetic partial sequences of P-Selectin glycoprotein ligand 1 (PSGL-1)

H. Kunz, H. Herzner, 2007 .

The development of synthetic antitumour vaccines from mucin glycopeptide antigens.

H. Kunz, Ulrika Westerlind, N. Gaidzik, 2013, Chemical Society reviews.

The Allyloxycarbonyl (Aloc) Moiety—Conversion of an Unsuitable into a Valuable Amino Protecting Group for Peptide Synthesis†

H. Kunz, C. Unverzagt, 1984 .

The Allyl Group as Mildly and Selectively Removable Carboxy‐Protecting Group for the Synthesis of Labile O‐Glycopeptides

H. Waldmann, H. Kunz, 1984 .

DIRECTED STEREOSELECTIVE SYNTHESIS OF ALPHA-N-ACETYL AND BETA-N-ACETYL NEURAMINIC ACID GALACTOSE DISACCHARIDES USING 2-CHLORO AND 2-FLUORO DERIVATIVES OF NEURAMINIC ACID ALLYL ESTER

H. Waldmann, H. Kunz, 1985 .

A fully synthetic glycopeptide antitumor vaccine based on multiple antigen presentation on a hyperbranched polymer.

H. Frey, E. Schmitt, H. Kunz, 2014, Chemistry.

Application of Ugi reactions in synthesis of divalent neoglycoconjugates: evidence that the sugars are presented in restricted conformation.

H. Kunz, P. Murphy, G. Fitzpatrick, 2001, Organic letters.

Carbohydrates as chiral templates: Stereoselective Strecker synthesis of D‐α‐amino nitriles and acids using O‐pivaloylated D‐galactosylamine as the auxiliary

H. Kunz, W. Sager, D. Schanzenbach, 1991 .

CpG‐Loaded Multifunctional Cationic Nanohydrogel Particles as Self‐Adjuvanting Glycopeptide Antitumor Vaccines

R. Zentel, E. Schmitt, H. Kunz, 2015, Advanced healthcare materials.

Oxacyclododecindione, a Novel Inhibitor of IL-4 Signaling from Exserohilum rostratum

T. Anke, J. Liermann, T. Opatz, 2008, The Journal of Antibiotics.

Stereoselective glycosylation of Alcohols and Silyl Ethers Using Glycosyl Fluorides and Boron Trifluoride Etherate

H. Kunz, W. Sager, 1985 .

Synthetic antitumor vaccines from tetanus toxoid conjugates of MUC1 glycopeptides with the Thomsen-Friedenreich antigen and a fluorine-substituted analogue.

E. Schmitt, H. Kunz, D. Kowalczyk, 2010, Angewandte Chemie.

STEREOSPECIFIC C-C-BOND FORMATION WITH RABBIT MUSCLE ALDOLASE - A CHEMOENZYMATIC SYNTHESIS OF (+)-EXO-BREVICOMIN

H. Waldmann, W. Vogt, H. Kunz, 1990 .

Synthesis of TN and T Antigen Glycopeptide Sequences of tumor‐associated MUC‐1 using S‐pent‐4‐enyl thioglycosides

H. Kunz, M. Leuck, 1997 .

Chemical and enzymatic synthesis of glycopeptides.

H. Kunz, M. Schultz, 2010, EXS.

Recent Developments in the Synthesis of Glycopeptides

H. Kunz, 1994 .

Synthesis of glycopeptides: a challenge for chemical selectivity

H. Kunz, C. Unverzagt, K. Bruch, 1994 .

Lewis Acid-Catalyzed Stereoselection on Carbohydrate Templates

H. Kunz, 1989 .

The Allyl Ester as Carboxy‐Protecting Group in the Stereoselective Construction of Neuraminic‐Acid Glycosides

H. Waldmann, H. Kunz, U. Klinkhammer, 1988 .

Synthesis of glycopeptides with tumor-associated antigen structure

H. Kunz, S. Friedrich-Bochnitschek, S. Birnbach, 1988 .

Diastereoselektive Strecker‐Synthese von α‐Aminonitrilen an Kohlenhydrat‐Matrices

H. Kunz, W. Sager, 1987 .

Effects of glycosylation on fragments of tumour associated human epithelial mucin MUC1.

P. Williams, M. Price, P. Braun, 1998, Bioorganic & medicinal chemistry.

Chemical and Chemoenzymatic Synthesis of Glycopeptide Selectin Ligands Containing Sialyl Lewis X Structures

H. Kunz, J. Bull, Maciej Pudelko, 2010, Chembiochem : a European journal of chemical biology.

Hetero-Diels-Alder reactions on a carbohydrate template: stereoselective synthesis of (S)-anabasin

H. Kunz, W. Pfrengle, 1989 .

Carbohydrates as Chiral Templates: Stereoselective Tandem Mannich‐Michael Reactions for the Synthesis of Piperidine Alkaloids

H. Kunz, W. Pfrengle, 1989 .

Synthesis of O-Glycopeptides of the Tumor-Associated TN- and T-Antigen Type and Their Binding to Bovine Serum Albumin†‡

H. Kunz, S. Birnbach, 1986 .

Stereocontrolled synthesis of D-α-hydroxy carboxylic acid from L-amino acids

H. Kunz, H. Lerchen, 1987 .

Hydrophilic photolabelling of glycopeptides from the murine liver-intestine (LI) cadherin recognition domain.

H. Kunz, H. Detert, S. Heiner, 2006, Bioorganic & medicinal chemistry.

A novel synthesis of chain-extended amino sugar derivatives through aza-Cope rearrangement of N -galactosyl- N -homoallylamines

H. Kunz, Sandrine Deloisy, 1998 .

Multiple Sialyl Lewisx N‐Glycopeptides: Effective Ligands for E‐Selectin

H. Kunz, G. Kretzschmar, W. Schmidt, 1996 .

Synthesis of Deoxy Sialyl Lewisx Analogues, Potential Selectin Antagonists

W. Stahl, H. Kunz, G. Kretzschmar, 1994 .

Glycosylation-Induced Asymmetric Synthesis of 1-Substituted Tetrahydroisoquinolines

H. Kunz, P. Allef, 2007 .

Synthetic MUC1 Antitumor Vaccine with Incorporated 2,3‐Sialyl‐T Carbohydrate Antigen Inducing Strong Immune Responses with Isotype Specificity

P. Besenius, E. Schmitt, H. Kunz, 2018, Chembiochem : a European journal of chemical biology.

Palladium-catalysed C–C coupling reactions in the enantioselective synthesis of 2,4-disubstituted 4,5-dehydropiperidines using galactosylamine as a stereodifferentiating auxiliary

H. Kunz, S. Knauer, 2005 .

Inhibitors of Inducible NO Synthase Expression: Total Synthesis of (S)‐Curvularin and Its Ring Homologues

U. Förstermann, D. Schollmeyer, T. Anke, 2008, ChemMedChem.

Allyl esters as carboxy protecting groups in the synthesis of O-glycopeptides

Herbert Waldmann, H. Waldmann, H. Kunz, 1989 .

3.1 – Protecting Groups

H. Waldmann, H. Kunz, 1991 .

Stereoselective Synthesis of Enantiomerically Pure Piperidine Derivatives by N‐Galactosylation of Pyridones

D. Schollmeyer, M. Follmann, H. Kunz, 2004 .

Stereoselective Synthesis of L‐Amino Acids via Strecker and Ugi Reactions on Carbohydrate Templates.

H. Kunz, W. Sager, W. Pfrengle, 1992 .

Stereoselective Synthesis of L-Amino Acids via Strecker and Ugi Reaktions on Carbohydrate Templates

H. Kunz, W. Sager, W. Pfrengle, 1991 .

Glycosylation-induced asymmetric synthesis: β-amino acid esters via Mannich reactions

H. Kunz, P. Allef, 2000 .

Carbohydrates as Chiral Templates: Stereoselective Synthesis of (R)- and (S)-α-Aminophosphonic Acid Derivatives

S. Laschat, H. Kunz, 1992 .

Total Synthesis of the Antifungal Natural Product Mollisin

T. Opatz, H. Kunz, J. Rheinheimer, 2013 .

Carbohydrates as Chiral Auxiliaries in Stereoselective Synthesis. New Synthetic Methods (90)

H. Kunz, K. Rück, 1993 .

Carbohydrates as chiral templates : diastereoselective synthesis of N-glycosyl-N-homoallylamines and β-amino acids from imines

S. Laschat, H. Kunz, 1991 .

Stereoselective glycosylation of Alcohols and Silyl Ethers Using Glycosyl Fluorides and Boron Trifluoride Etherate

H. Kunz, W. Sager, 1985 .

Carbohydrate Auxiliaries in Stereoselective Syntheses of Decahydroquinoline Alkaloids

H. Kunz, M. Weymann, S. Knauer, 2002 .

Asymmetric synthesis on carbohydrate templates: stereoselective Ugi-synthesis of .alpha.-amino acid derivatives

H. Kunz, W. Pfrengle, 1988 .

Reversal of asymmetric induction in stereoselective Strecker synthesis on galactosyl amine as the chiral matrix

H. Kunz, W. Sager, W. Pfrengle, 1988 .

Investigation of Diketopiperazines Containing a Guanidino‐Functionalized Sidechain as Potential Catalysts of Enantioselective Strecker Reactions

D. Schollmeyer, H. Kunz, C. Becker, 2005 .

Enantioselective strecker reaction catalyzed by an organocatalyst lacking a hydrogen-bond-donor function.

D. Schollmeyer, H. Kunz, M. Negru, 2007, Angewandte Chemie.

Enantioselective Organocatalysis of Strecker and Mannich Reactions Based on Carbohydrates

H. Kunz, C. Becker, C. Hoben, 2007 .

Auxiliary-controlled stereoselective enolate protonation: Enantioselective synthesis of cis and trans annulated decahydroquinoline alkaloids

H. Kunz, M. Weymann, Martin Schultz-Kukula, 1998 .

ENANTIOSELECTIVE SYNTHESES OF 2-ALKYL-, 2,6-DIALKYLPIPERIDINES AND INDOLIZIDINE ALKALOIDS THROUGH DIASTEREOSELECTIVE MANNICH-MICHAEL REACTIONS

D. Schollmeyer, H. Kunz, M. Weymann, 1997 .

Synthesis of a polymer-bound galactosylamine and its application as an immobilized chiral auxiliary in stereoselective syntheses of piperidine and amino acid derivatives.

H. Kunz, G. Zech, 2004, Chemistry.

Glycosidsynthese mit 2,3,4,6‐Tetra‐O‐pivaloyl‐α‐D‐glucopyrancsylbromid

H. Kunz, A. Harréus, 1982 .

Carbohydrates as Stereodifferentiating Auxiliaries

H. Kunz, Alexander Stoye, 2017 .

Stereoselective Synthesis of 2-Substituted Pyrrolidines

H. Kunz, H. Tietgen, Sandrine Deloisy, 2000 .

Glycosylation-induced Asymmetric Synthesis: -Amino Acid Esters via Mannich Reactions.

H. Kunz, P. Allef, 2000 .

Solid-Phase Synthesis of a Sialyl-Tn-Glycoundecapeptide of the MUC1 Repeating Unit†

H. Kunz, B. Liebe, 1997 .

Sugars as Chiral Auxiliaries

H. Kunz, B. Furman, G. Zech, 2007 .

Asymmetric Mannich Synthesis of β‐Amino Acids with Two New Stereogenic Centers at the α and β Positions

A. Burgard, H. Kunz, D. Schanzenbach, 1997 .

Carbohydrates as Chiral Templates: Stereoselective Synthesis of β‐Amino Acids

H. Kunz, D. Schanzenbach, 1989 .

3.13 Carbohydrate Derived Auxiliaries: Amino Sugar and Glycosylamine Auxiliaries

H. Kunz, J. Bull, I. Strassnig, 2012 .

Carbohydrates as Chiral Templates: Stereoselective Synthesis of (R)- and (S)-α-Aminophosphonic Acid Derivatives.

S. Laschat, H. Kunz, 1992 .

Synthesis of glycopeptides containing carbohydrate and Peptide recognition motifs.

H. Kunz, M. Schultz, H. Herzner, 2000, Chemical reviews.

D-Glucose as a Pentavalent Chiral Scaffold

T. Opatz, H. Kunz, S. Henke, 2003 .

Carbohydrates as chiral templates: reactivity and stereoselectivity of carbohydrate ester enolates

H. Kunz, J. Mohr, 1988 .

Diastereoselective Diels–Alder Reaction on Carbohydrate Matrices

H. Kunz, B. Müller, D. Schanzenbach, 1987 .

A New Activating Principle in Glycoside Synthesis Based on Electrophile-Induced Lactonization of Glucosyl 4-Pentenoates

H. Kunz, M. Schultz, P. Wernig, 1990 .

Dipolar recoupling in NOESY-type 1H-1H NMR experiments under HRMAS conditions.

H. Spiess, H. Kunz, K. Thieme, 2002, Organic letters.

A facile cleavage of allyl ethers on solid phase

T. Opatz, H. Kunz, 2000 .

Stereoselective synthesis of benzomorphan derivatives with perpivaloylated galactose as the chiral auxiliary.

H. Kunz, Ellen Klegraf, S. Knauer, 2006, Angewandte Chemie.

Stereoselective synthesis of chiral piperidine derivatives employing arabinopyranosylamine as the carbohydrate auxiliary

H. Kunz, Birgit Kranke, 2006 .

Desymmetrization Reactions on 4-Pyridone Using Carbohydrate Templates

M. Follmann, H. Kunz, 1998 .

Stereoselective synthesis of amino acid derivatives using carbohydrates as templates

S. Laschat, H. Kunz, W. Sager, 1993 .

Leopold Horner (1911–2005): Nestor of Preparative Organic Chemistry

H. Kunz, 2005 .

Fluorenylmethoxycarbonyl‐N‐methylamino Acids Synthesized in a Flow Tube‐in‐Tube Reactor with a Liquid–Liquid Semipermeable Membrane

H. Löwe, H. Kunz, Annette E. Buba, 2013 .

Total Synthesis of the Antifungal Natural Product Mollisin.

T. Opatz, H. Kunz, J. Rheinheimer, 2014 .

β-Branched α-Halo Carboxylic Acid Derivatives via Stereoselective 1,4 Addition of Dialkylaluminum Chlorides to α,β-Unsaturated N-Acyloxazolidinones

H. Kunz, K. Rück-Braun, A. Stamm, 1997 .

Synthesis of Glycopeptides with Lewisa Antigen Side Chain and HIV Peptide T Sequence Using the Trichloroethoxycarbonyl/Allyl Ester Protecting Group Combination

J. März, H. Kunz, 1992 .

Carbohydrate scaffolds for combinatorial syntheses that allow selective deprotection of all four positions independent of the sequence.

H. Kunz, Udo Huenger, Janina Ohnsmann, 2004, Angewandte Chemie.

Amino Sugars and Glycosylamines as Tools in Stereoselective Synthesis

H. Kunz, S. Knauer, Birgit Kranke, 2004 .

Stereoselective solid-phase synthesis of chiral piperidine derivatives by using an immobilized galactose auxiliary.

H. Kunz, G. Zech, 2003, Angewandte Chemie.

Chiral Auxiliaries in Cycloadditions

H. Kunz, K. Rück-Braun, 1999 .

Enantioselective Allylic Substitution Using a Novel (Phosphino-α-d-glucopyrano-oxazoline)palladium Catalyst

H. Kunz, B. Glaeser, 1998 .

Stereoselective syntheses using carbohydrates as chiral auxiliaries

H. Kunz, 1995 .

Carbohydrates as Chiral Auxiliaries. [2+2) Cycloadditions of Ketenes to Enol Ethers

H. Kunz, I. Ganz, 1994 .

Stereoselective Conjugate Addition of Organoaluminum Chlorides to α,β-Unsaturated Carboxylic Acid Derivatives

H. Kunz, K. Rück, 1993 .

A Bicyclic Carbohydrate Oxazolidinone Template for Stereoselective 1,4-Additions of Organoaluminium Chlorides to Unsaturated Carboxylic Acid Derivatives

H. Kunz, K. Rück, 1992 .

Carbohydrates as Chiral Templates: Stereoselective Diels-Alder Synthesis with Dienes of Differing Reactivity

H. Kunz, Wolfgang Stähle, 1991 .

Carbohydrates as chiral templates : stereoselective synthesis of chiral homoallyl amines and β-amino acids

S. Laschat, H. Kunz, 1990 .

Carbohydrates as chiral templates : stereoselective synthesis of (R)-homoallyl amines using L-fucose as the auxiliary formally enantiomeric to D-galactose

S. Laschat, H. Kunz, 1990 .

Carbohydrates as chiral templates: asymmetric ugi-synthesis of alpha-amino acids using galactosylamines as the chiral matrices

H. Kunz, W. Pfrengle, 1988 .

C-Glycosyl amino acids through hydroboration-cross-coupling of exo-glycals and their application in automated solid-phase synthesis.

H. Löwe, D. Schollmeyer, H. Kunz, 2013, Chemistry.

Emil Fischer--unequalled classicist, master of organic chemistry research, and inspired trailblazer of biological chemistry.

H. Kunz, Horst Kunz, 2002, Angewandte Chemie.

Stereoselective synthesis of C-glycosyl compounds via Michael addition of trimethylsilyl enol ethers and enamines to hex-1-enopyran-3-uloses

H. Kunz, B. Müller, J. Weissmüller, 1987 .

Synthese von Glycopeptiden

H. Kunz, 1984 .

Glycosylamines as Auxiliaries in Stereoselective Syntheses of Chiral Amino Compounds

H. Kunz, H. Tietgen, Martin Schultz-Kukula, 2007 .

Synthesis of Sulfated Lex-Trisaccharides†

W. Stahl, H. Kunz, G. Kretzschmar, 1995 .

Synthese eines β-Mannosyl-Chitobiosyl-Asparagin-Konjugates—eines zentralen Elements der Core-Region von N-Glycoproteinen†

W. Günther, H. Kunz, 1990 .

Synthesis of β-D-mannosides from β-D-glucosides via an intramolecular SN2 reaction at C-2

W. Günther, H. Kunz, 1992 .

Ceric Ammonium Nitrate – a versatile oxidizing reagent

H. Kunz, K. Rück, 1994 .

Solid‐Phase Synthesis of a Tumor‐Associated Sialyl‐TN Antigen Glycopeptide with a Partial Sequence of the “Tandem Repeat” of the MUC‐1 Mucin

H. Kunz, B. Liebe, 1997 .

Stereoselective synthesis of enantiomerically pure nupharamine alkaloids from castoreum.

H. Kunz, André Fischer, M. Weymann, 2009, Angewandte Chemie.

Stereoselective syntheses of piperidinones and their modification by organometallic coupling reactions.

H. Kunz, Birgit Kranke, 2007, Organic & biomolecular chemistry.

Synthesis of glycopeptides with the TN and T antigen structures, and their coupling to bovine serum albumin.

H. Kunz, S. Birnbach, P. Wernig, 1990, Carbohydrate research.

Synthetic glycopeptides from the E-selectin ligand 1 with varied sialyl Lewis(x) structure as cell-adhesion inhibitors of E-selectin.

D. Vestweber, H. Kunz, D. Kowalczyk, 2007, Angewandte Chemie.

Synthesis of the all‐L‐Configurated Cyclohexadepsipeptide cyclo‐[L‐Val‐L‐Lac]3 by the Peoc/Acid Chloride Method

H. Kunz, H. Lerchen, 1984 .

Coupling of Sterically Hindered Peptide Bonds—A Renaissance of the Acid Chloride Method.

H. Kunz, Hans-Heinrich D Bechtolsheimer, 1982 .

Mixed Dialkylaluminum Chlorides and Mixed Trimethylorganoaluminates in Chemoselective 1,4 Addition Reactions to Alkylidene Malonic Acid Diethyl Ester

H. Kunz, S. Maas, 2000 .

The 1,3‐Dithian‐2‐ylmethoxycarbonyl (Dmoc) Moiety–A Protecting Group for the Amino Function in Peptide Synthesis

H. Kunz, R. Barthels, 1982 .

Natural product and material chemistries--separated forever?

K. Müllen, H. Kunz, 2013, Journal of the American Chemical Society.

N-glycosyl amides: removal of the anomeric protecting group and conversion into glycosyl donors.

H. Kunz, Norbert Pleuss, 2003, Angewandte Chemie.

N‐Glycosyl Amides: Removal of the Anomeric Protecting Group and Conversion into Glycosyl Donors.

H. Kunz, Norbert Pleuss, 2003 .

Reduced Breast Tumor Growth after Immunization with a Tumor-Restricted MUC1 Glycopeptide Conjugated to Tetanus Toxoid

Marcus Schmidt, P. Besenius, E. Schmitt, 2018, Cancer Immunology Research.

The Development of Vaccines from Synthetic Tumor‐Associated Mucin Glycopeptides and their Glycosylation‐Dependent Immune Response

P. Besenius, E. Schmitt, H. Kunz, 2021, Chemical record.

Carbohydrates as Multifunctional Chiral Scaffolds in Combinatorial Synthesis.

T. Opatz, H. Kunz, S. Henke, 1998, Angewandte Chemie.

Combinatorial synthesis of amino acid- and peptide-carbohydrate conjugates on solid phase

T. Opatz, H. Kunz, Christopher Kallus, 2004 .

Advances in N‐ and O‐Glycopeptide Synthesis – A Tool to Study Glycosylation and Develop New Therapeutics

H. Kunz, Ulrika Westerlind, 2011 .

Biomimetic synthesis of the tumor-associated (2,3)-sialyl-T antigen and its incorporation into glycopeptide antigens from the mucins MUC1 and MUC4.

H. Kunz, Constanze Brocke, S. Dziadek, 2004, Chemistry.

Stereoselektive Glycosylierung von Steroidalkoholen mit 2,3,4,6‐Tetra‐O‐privaloyl‐α‐D‐glucopyranosylbromid (Pivalobromglucose) und 2,3,4,6‐Tetra‐O‐(o‐toluoyl)‐α‐D‐glucopyranosylbromid

H. Kunz, A. Harréus, 1986 .

Total synthesis of the glycopeptide recognition domain of the P-selectin glycoprotein ligand 1.

H. Kunz, D. Kowalczyk, Katharina Baumann, 2008, Angewandte Chemie.

Synthetic glycopeptides for the development of tumour‐selective vaccines

H. Kunz, 2003, Journal of peptide science : an official publication of the European Peptide Society.

Metal ion-promoted activation of amino acid esters of carbohydrates in the synthesis of peptides

H. Kunz, R. Kullmann, 1992 .

β‐Mannosides from β‐Glucosides by Intramolecular Nucleophilic Substitution with Inversion of Configuration

W. Günther, H. Kunz, 1988 .

Chemistry of glycopeptides

H. Kunz, Jörg Habermann, B. Löhr, 1999 .

Chemoenzymatic-Chemical Synthesis of a (2-3)-Sialyl T Threonine Building Block and Its Application to the Synthesis of the N-Terminal Sequence of Leukemia-Associated Leukosialin (CD 43).

A. Liese, H. Kunz, G. Dudziak, 2001, Angewandte Chemie.

Tumor-associated MUC1 tandem-repeat glycopeptide microarrays to evaluate serum- and monoclonal-antibody specificity.

H. Waldmann, C. Niemeyer, E. Schmitt, 2009, Angewandte Chemie.

Synthetic vaccines consisting of tumor-associated MUC1 glycopeptide antigens and bovine serum albumin.

H. Kunz, D. Kowalczyk, S. Dziadek, 2005, Angewandte Chemie.

Synthesis of tumor-associated glycopeptide antigens.

H. Kunz, Constanze Brocke, 2002, Bioorganic & medicinal chemistry.

Mild Synthesis of Protected α‐D‐Glycosyl Iodides

H. Kunz, Giovanni Palumbo, Silvana Pedatella, 1999 .

Synthesis of a β‐Mannosyl‐Chitobiosyl‐Asparagine Conjugate—a Central Core Region Unit of the N‐Glycoproteins

W. Günther, H. Kunz, 1990 .

Synthetic Tumor‐Associated Glycopeptide Antigens from the Tandem Repeat Sequence of the Epithelial Mucin MUC4.

H. Kunz, Constanze Brocke, 2004 .

NEW ENZYMATIC METHODS FOR THE SELECTIVE FUNCTIONALIZATION OF CARBOHYDRATE-DERIVATIVES

H. Waldmann, P. Braun, H. Kunz, 1992 .

Synthesis of active principles from the leaves of Moringa oleifera using S-pent-4-enyl thioglycosides

H. Kunz, Michael Leuck, Horst Kunz, 1998 .

β-Mannoside aus β-Glucosiden durch intramolekulare nucleophile Substitution unter Konfigurationsumkehr†

W. Günther, H. Kunz, 1988 .

Synthesis of Biologically Interesting Glycopeptides

H. Kunz, W. Brill, 1992 .

Stereoselective Synthesis of β-1-O-Acyl Derivatives of Carbohydrates: An Application of the Cesium Effect.

H. Kunz, P. Wernig, R. Kullmann, 1992 .

Synthesis of Selectively Deprotectable Asparagine Glycoconjugates with a Lewisa Antigen Side Chain

J. März, H. Kunz, 1992 .

Glycopeptides of biological interest: A challenge for chemical synthesis

H. Kunz, 1993 .

Antitumor Vaccines Based on Synthetic Mucin Glycopeptides

H. Kunz, Ulrika Westerlind, 2012 .

Synthesis of glycopeptide derivatives of Peptide T on a solid phase using an allylic linkage

J. März, H. Kunz, W. Kosch, 1994 .

Synthesis of a Tumor-Associated2,3-Sialyl-T Glycododecapeptide Antigen from the Tandem Repeat Regionof the Mucin MUC1

H. Kunz, S. Dziadek, 2003 .

Synthesis of tumor-associated glycopeptide antigens for the development of tumor-selective vaccines.

H. Kunz, S. Dziadek, 2004, Chemical record.

Chemoenzymatic-Chemical Synthesis of a (2-3)-Sialyl T Threonine Building Block and Its Application to the Synthesis of the N-Terminal Sequence of Leukemia-Associated Leukosialin (CD 43) This work was supported by the Deutsche Forschungsgemeinschaft, the Stiftung Rheinland Pfalz für Innovation, and t

A. Liese, H. Kunz, G. Dudziak, 2001, Angewandte Chemie.

Synthesis and Structural Model of an α(2,6)‐Sialyl‐T Glycosylated MUC1 Eicosapeptide under Physiological Conditions

C. Griesinger, H. Kunz, U. Reinscheid, 2006 .

Enzymatic glycosylation of O-glycopeptides

H. Kunz, M. Schultz, 1992 .

CONSTRUCTION OF DISACCHARIDE N-GLYCOPEPTIDES - SYNTHESIS OF THE LINKAGE REGION OF THE TRANSMEMBRANE-NEURAMINIDASE OF AN INFLUENZA VIRUS

H. Waldmann, H. Kunz, 1985 .

Synthesis of an RGD‐Sialyl‐LewisX Glycoconjugate: A New Highly Active Ligand for P‐Selectin**

H. Kunz, E. Bartnik, G. Kretzschmar, 1995 .

Regioselective Glycosylation of Glucosamine and Galactosamine Derivates Using O-Pivaloyl Galactosyl Donors

H. Kunz, W. Pfrengle, S. Friedrich-Bochnitschek, 2003 .

Gold Catalysis in GlycosylationReactions

H. Kunz, R. Fitzner, S. Götze, 2009 .

Synthesis of α‐fucosyl glycosides and disaccharides using 4‐methoxybenzyl (Mpm) protected fucosyl donors

H. Kunz, C. Unverzagt, 1992 .

Specificity of human natural antibodies referred to as anti-Tn.

N. Bovin, O. Blixt, Y. Knirel, 2020, Molecular immunology.

Mucin Glycopeptide‐Protein Conjugates – Promising Antitumor Vaccine Candidates

H. Kunz, M. Glaffig, B. Palitzsch, 2015 .

Towards the Development of Antitumor Vaccines: A Synthetic Conjugate of a Tumor-Associated MUC1 Glycopeptide Antigen and a Tetanus Toxin Epitope.

W. Dippold, S. Keil, H. Kunz, 2001, Angewandte Chemie.

Synthetic Glycopeptides for the Development of Antitumour Vaccines

H. Kunz, S. Dziadek, C. G. Espínola, 2003 .

Synthetic vaccines of tumor-associated glycopeptide antigens by immune-compatible thioether linkage to bovine serum albumin.

H. Kunz, T. Becker, S. Wittrock, 2007, Angewandte Chemie.

Saccharide-induced peptide conformation in glycopeptides of the recognition region of LI-cadherin.

H. Kunz, A. Kuhn, 2007, Angewandte Chemie.

A fully synthetic vaccine consisting of a tumor-associated glycopeptide antigen and a T-cell epitope for the induction of a highly specific humoral immune response.

E. Schmitt, H. Kunz, S. Dziadek, 2005, Angewandte Chemie.

Synthetic Glycopeptides for the Development of Antitumor Vaccines.

H. Kunz, S. Dziadek, C. G. Espínola, 2003 .

Selective enzymatic removal of protecting functions : heptyl esters as carboxy protecting groups in glycopeptide synthesis

H. Waldmann, P. Braun, H. Kunz, 1992 .

Synthetic Glycopeptides for the Development of Tumor‐Selective Vaccines

H. Kunz, 2004 .

The p‐Nitrocinnamyloxycarbonyl (Noc) Moiety—an Acid‐stable Amino‐protecting Group Removable under Neutral Conditions for Peptide and Glycopeptide Synthesis

J. März, H. Kunz, 1988 .

Archaea analogue thiolipids for tethered bilayer lipid membranes on ultrasmooth gold surfaces.

Wolfgang Knoll, Stefan M Schiller, Katherine S. Lovejoy, 2003, Angewandte Chemie.

Synthetic multivalent glycopeptide-lipopeptide antitumor vaccines: impact of the cluster effect on the killing of tumor cells.

Yan‐Mei Li, H. Kunz, Yu-Fen Zhao, 2014, Angewandte Chemie.

Microarray Analysis of Antibodies Induced with Synthetic Antitumor Vaccines: Specificity against Diverse Mucin Core Structures.

Jia Liu, Mengji Lu, E. Schmitt, 2017, Chemistry.

Variation of the glycosylation pattern in MUC1 glycopeptide BSA vaccines and its influence on the immune response.

Yan‐Mei Li, Lei Shi, H. Kunz, 2012, Angewandte Chemie.

Synthesis of Tn/T Antigen MUC1 Glycopeptide BSA Conjugates and Their Evaluation as Vaccines

Peng Zou, Lei Shi, H. Kunz, 2011 .

Fully synthetic self-adjuvanting thioether-conjugated glycopeptide-lipopeptide antitumor vaccines for the induction of complement-dependent cytotoxicity against tumor cells.

Yan‐Mei Li, Lei Shi, H. Kunz, 2013, Chemistry.

Self-adjuvanting synthetic antitumor vaccines from MUC1 glycopeptides conjugated to T-cell epitopes from tetanus toxoid.

Yan‐Mei Li, H. Kunz, Yu-Fen Zhao, 2013, Angewandte Chemie.

A fully synthetic four-component antitumor vaccine consisting of a mucin glycopeptide antigen combined with three different T-helper-cell epitopes.

E. Schmitt, H. Kunz, M. Glaffig, 2014, Angewandte Chemie.

Synthesis of the Glycopeptide Partial Sequence A80–A84 of Human Fibroblast Interferon

H. Waldmann, H. Kunz, 1985 .

Synthesis of the all-L-Configurated Cyclotetradepsipeptide cyclo[-L-Val-L-Lac-]2 by the Combined Protection/Activation Method with the 2,4-Bis(methylthio)phenoxycarbonyl Group†

H. Kunz, H.-J. Lasowski, 1986 .

β-Alkyl and β-Alkyl-α-Hydroxy Carboxylic Acid Derivatives from Radical or Ionic 1,4 Addition of Dialkylaluminum Chlorides to α,β-Unsaturated N-Acyl Urethanes†‡

H. Kunz, K. Rück, 1991 .

Fragment condensation on solid-phase in the synthesis of an amphiphilic glycopeptide from the homophilic recognition domain of epithelial cadherin 1

H. Kunz, Jörg Habermann, J. Habermann, 1998 .

Solid-phase synthesis of a glycopeptide from the homophilic recognition domain of epithelial cadherin 1 using a O-pentafluorophenyluronium salt

H. Kunz, Jörg Habermann, J. Habermann, 1998 .

GLYCOPEPTIDE SYNTHESIS USING O-PENTAFLUOROPHENYLURONIUM SALTS AS NOVEL CONDENSING REAGENTS

H. Kunz, Jörg Habermann, 1998 .

Synthesis and structural model of an alpha(2,6)-sialyl-t glycosylated MUC1 eicosapeptide under physiological conditions.

C. Griesinger, H. Kunz, U. Reinscheid, 2006, Chemistry.

Allyl ester as temporary protecting group for the β‐carboxy function of aspartic acid

H. Waldmann, H. Kunz, C. Unverzagt, 2009 .

Antibody Induction Directed against the Tumor‐Associated MUC4 Glycoprotein

E. Schmitt, H. Kunz, N. Stergiou, 2015, Chembiochem : a European journal of chemical biology.

Glycopeptide-functionalized gold nanoparticles for antibody induction against the tumor associated mucin-1 glycoprotein.

Edgar Schmitt, Roberto Fiammengo, E. Schmitt, 2016, Bioorganic & medicinal chemistry.

Preparation of Biomolecule Microstructures and Microarrays by Thiol–ene Photoimmobilization

H. Waldmann, C. Niemeyer, H. Engelkamp, 2010, Chembiochem : a European journal of chemical biology.

Water-soluble polymers coupled with glycopeptide antigens and T-cell epitopes as potential antitumor vaccines.

R. Zentel, E. Schmitt, H. Kunz, 2013, Angewandte Chemie.

Synthetic Antitumor Vaccines Through Coupling of Mucin Glycopeptide Antigens to Proteins

H. Kunz, M. Glaffig, 2018 .

Synthesis and Biological Evaluation of a Multiantigenic Tn/TF‐Containing Glycopeptide Mimic of the Tumor‐Related MUC1 Glycoprotein

A. Delmas, V. Piller, H. Kunz, 2006, ChemMedChem.

Synthetic MUC1 Antitumor Vaccine Candidates with Varied Glycosylation Pattern Bearing R/S‐configured Pam3CysSerLys4

Yong-Xiang Chen, Yan‐Mei Li, Lei Shi, 2016, Chembiochem : a European journal of chemical biology.

Synthesis of Active Principles from the Leaves of Moringa oleifera Using S-Pent-4-enyl Thioglycosides.

H. Kunz, M. Leuck, 1999 .

Convenient Synthesis of Biologically Important Retinoids

H. Kunz, H. Biesalski, Michael John, 1995 .

Sulfated and non-sulfated glycopeptide recognition domains of P-selectin glycoprotein ligand 1 and their binding to P- and E-selectin.

D. Vestweber, H. Kunz, D. Kowalczyk, 2009, Angewandte Chemie.

Synthesis of Dendrimeric Tumor-AssociatedMucin-Type Glycopeptide Antigens

H. Kunz, Anton Kaiser, T. Becker, 2009 .

Protein kinase CK2 governs the molecular decision between encephalitogenic TH17 cell and Treg cell development

H. Schild, F. Zipp, A. Waisman, 2016, Proceedings of the National Academy of Sciences.

Asymmetric Synthesis on Carbohydrate Templates: Stereoselective Ugi Synthesis of α-Amino Acid Derivatives.

H. Kunz, W. Pfrengle, 1988 .

The (2-phenyl-2-trimethylsilyl)ethyl-(PTMSEL)-linker in the synthesis of glycopeptide partial structures of complex cell surface glycoproteins.

H. Kunz, M. Wagner, S. Dziadek, 2003, Chemistry.

A Novel Allylic Anchor for Solid‐Phase Synthesis—Synthesis of Protected and Unprotected O‐Glycosylated Mucin‐Type Glycopeptides

O. Seitz, H. Kunz, 1995 .

Synthetic vaccines from tumor-associated glycopeptide antigens.

H. Kunz, Ulrika Westerlind, 2011, Chimia.

2-(TRIPHENYLPHOSPHONIO)ETHOXYCARBONYL (PEOC) MOIETY; AN ACID STABLE HYDROXY PROTECTION GROUP

H. Kunz, Hans-Heinrich D Bechtolsheimer, 1982 .

The 2‐(2‐Pyridyl)ethoxycarbonyl‐(Pyoc) Residue—An Acid‐ and Base‐Stable, Hydrophilic Protecting Group for the Amino Function in Peptide Synthesis

H. Kunz, R. Barthels, 1983 .

Solid Phase Synthesis of Peptides and Glycopeptides on Polymeric Supports with Allylic Anchor Groups

H. Kunz, B. Dombo, 1988 .

2-(Pyridyl)ethyl Esters as Secure yet Readily Removable Polarophilic Carboxy-Protection in Peptide Synthesis†‡

H. Kunz, M. Kneip, 1984 .

2-(PYRIDYL)ETHYL ESTER AS SAFE AND EASILY DETACHED POLAROPHILIC CARBOXY PROTECTIVE GROUP IN PEPTIDE SYNTHESIS

H. Kunz, M. Kneip, 1985 .

Oligosaccharide recognition by selectins: Synthesis and biological activity of multivalent sialyl lewis-X ligands

H. Kunz, E. Bartnik, G. Kretzschmar, 1995 .

Allyl Esters as Carboxy Protecting Groups in the Synthesis of O-Glycopeptides.

H. Waldmann, H. Kunz, S. Friedrich-Bochnitschek, 1989 .

Glycopeptide Synthesis in Solution and on the Solid Phase

G. Hart, B. Ernst, H. Kunz, 2008 .

ALLYLOXYCARBONYL(ALOC) PART - CONVERSION OF AN UNSUITABLE AMINO PROTECTIVE GROUP TO A USEFUL ONE FOR PEPTIDE SYNTHESIS

H. Kunz, C. Unverzagt, 1984 .

ChemInform Abstract: Synthetic Inhibitors of Cell Adhesion: A Glycopeptide from E-Selectin Ligand 1 (ESL-1) with the Arabino Sialyl Lewisx Structure.

W. Dippold, D. Vestweber, H. Kunz, 2002 .

Chemoselective Removal of Protecting Groups from O-Glycosyl Amino Acid and Peptide (Methoxyethoxy)ethyl Esters Using Lipases and Papain.

P. Braun, H. Kunz, M. Schultz, 1996, The Journal of organic chemistry.

Enzymatic Hydrolysis of Hydrophilic Diethyleneglycol and Polyethyleneglycol Esters of Peptides and Glycopeptides by Lipases.

P. Braun, H. Kunz, D. Kowalczyk, 1994 .

A Carbohydrate-Based Julia–Kocienski Reagent for Syntheses of Chain-Extended and C-Linked Saccharides

H. Kunz, J. Bull, 2014, Synthesis.

Synthesis and biological activity of novel sialyl-lewisX conjugates

H. Kunz, D. Seiffge, W. Schmidt, 1996 .

Fluorenylmethoxycarbonyl‐Protected O‐Glycosyl‐N‐methyl Amino Acids: Building Blocks for the Synthesis of Conformationally Tuned Glycopeptide Antigens

H. Löwe, H. Kunz, Annette E. Buba, 2015 .

Glycoside Synthesis via Electrophile‐Induced Activation of N‐Allyl Carbamates.

H. Kunz, Jörg Zimmer, 1993 .

Glycoside synthesis via electrophile-induced activation of N-allyl carbamates

H. Kunz, Jörg Zimmer, 1993 .

Enzymatic Cleavage of tert-Butyl Esters: Thermitase-Catalyzed Deprotection of Peptides and O-Glycopeptides

P. Hermann, H. Kunz, M. Schultz, 1992 .

Selective Enzymatic Removal of Protecting Functions: Heptyl Esters as Carboxy Protecting Groups in Glycopeptide Synthesis

H. Waldmann, P. Braun, H. Kunz, 1990 .

The development of synthetic antitumour vaccines from mucin glycopeptide antigens.

H. Kunz, Ulrika Westerlind, N. Gaidzik, 2013, Chemical Society reviews.

Synthetic glycopeptides for the development of cancer vaccines.

Angela Liakatos, H. Kunz, 2007, Current opinion in molecular therapeutics (Print).

Inside Back Cover: Microarray Analysis of Antibodies Induced with Synthetic Antitumor Vaccines: Specificity against Diverse Mucin Core Structures (Chem. Eur. J. 16/2017)

Jia Liu, Mengji Lu, E. Schmitt, 2017 .