| Year |
Citation |
Score |
| 2015 |
Strassnig I, Körber K, Hünger U, Kunz H. Stereoselective Total Synthesis of the Diastereomeric Tricyclic Alkaloids Tetraponerine-7 and Tetraponerine-8 Using O-Pivaloylated d-Arabinopyranosylamine as the Common Auxiliary Synthesis (Germany). DOI: 10.1055/S-0034-1380215 |
0.374 |
|
| 2015 |
Buba AE, Löwe H, Kunz H. Fluorenylmethoxycarbonyl-Protected O-Glycosyl-N-methyl Amino Acids: Building Blocks for the Synthesis of Conformationally Tuned Glycopeptide Antigens European Journal of Organic Chemistry. 2015: 5764-5774. DOI: 10.1002/Ejoc.201500929 |
0.375 |
|
| 2013 |
Koch S, Schollmeyer D, Löwe H, Kunz H. C-Glycosyl amino acids through hydroboration-cross-coupling of exo-glycals and their application in automated solid-phase synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 7020-41. PMID 23553723 DOI: 10.1002/Chem.201300150 |
0.366 |
|
| 2013 |
Schwolow S, Kunz H, Rheinheimer J, Opatz T. Total synthesis of the antifungal natural product mollisin European Journal of Organic Chemistry. 6519-6524. DOI: 10.1002/Ejoc.201301088 |
0.489 |
|
| 2012 |
Klegraf E, Kunz H. Stereoselective synthesis of 3-substituted and 3,4-disubstituted piperidine und piperidin-2-one derivatives Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences. 67: 389-405. DOI: 10.1515/Znb-2012-0413 |
0.394 |
|
| 2011 |
Cai H, Huang ZH, Shi L, Zhao YF, Kunz H, Li YM. Towards a fully synthetic MUC1-based anticancer vaccine: efficient conjugation of glycopeptides with mono-, di-, and tetravalent lipopeptides using click chemistry. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 6396-406. PMID 21538615 DOI: 10.1002/Chem.201100217 |
0.314 |
|
| 2010 |
Weinrich D, Köhn M, Jonkheijm P, Westerlind U, Dehmelt L, Engelkamp H, Christianen PC, Kuhlmann J, Maan JC, Nüsse D, Schröder H, Wacker R, Voges E, Breinbauer R, Kunz H, et al. Preparation of biomolecule microstructures and microarrays by thiol-ene photoimmobilization. Chembiochem : a European Journal of Chemical Biology. 11: 235-47. PMID 20043307 DOI: 10.1002/Cbic.200900559 |
0.423 |
|
| 2010 |
Pudelko M, Kowalczyk D, Kunz H. Regioselective deacetylation and glycosylation in the synthesis of the sialyl lewis0 X tetrasaccharide, a key component of the recognition site of PSGL-1 Synlett. 3023-3026. DOI: 10.1055/S-0030-1259054 |
0.301 |
|
| 2010 |
KUNZ H, UNVERZAGT C, DOMBO B, KOSCH W, WALDMANN H. ChemInform Abstract: Synthesis of Glycopeptide Partial Structures of Virus Coat Glycoproteins Cheminform. 26: no-no. DOI: 10.1002/chin.199515318 |
0.331 |
|
| 2010 |
WALDMANN H, HEUSER A, BRAUN P, SCHULTZ M, KUNZ H. ChemInform Abstract: New Enzymic Methods for the Selective Functionalization of Carbohydrate Derivatives Cheminform. 24: no-no. DOI: 10.1002/chin.199333292 |
0.321 |
|
| 2010 |
WALDMANN H, HEUSER A, BRAUN P, KUNZ H. ChemInform Abstract: New Enzymatic Protecting Group Techniques for Peptide and Carbohydrate Chemistry. Cheminform. 24: no-no. DOI: 10.1002/chin.199313067 |
0.378 |
|
| 2010 |
BRAUN P, WALDMANN H, VOGT W, KUNZ H. ChemInform Abstract: Selective Enzymatic Removal of Protecting Groups: n-Heptyl Esters as Carboxy Protecting Functions in Peptide Synthesis. Cheminform. 22: no-no. DOI: 10.1002/chin.199117251 |
0.443 |
|
| 2010 |
SCHULTZ M, WALDMANN H, KUNZ H, VOGT W. ChemInform Abstract: Chemoenzymatic “Chiral-Pool” Synthesis of (+)-exo-Brevicomin from Carbohydrates Using Fructose 1,6-Diphosphate Aldolase. Cheminform. 22: no-no. DOI: 10.1002/chin.199102093 |
0.421 |
|
| 2009 |
Stoye A, Quandt G, Brunnhöfer B, Kapatsina E, Baron J, Fischer A, Weymann M, Kunz H. Stereoselective synthesis of enantiomerically pure nupharamine alkaloids from castoreum. Angewandte Chemie (International Ed. in English). 48: 2228-30. PMID 19199304 DOI: 10.1002/Anie.200805606 |
0.35 |
|
| 2009 |
KUNZ H, WALDMANN H, UNVERZAGT C. Allyl ester as temporary protecting group for the β-carboxy function of aspartic acid International Journal of Peptide and Protein Research. 26: 493-497. DOI: 10.1111/J.1399-3011.1985.Tb01016.X |
0.434 |
|
| 2009 |
Götze S, Fitzner R, Kunz H. Gold catalysis in glycosylation reactions Synlett. 3346-3348. DOI: 10.1055/S-0029-1218356 |
0.356 |
|
| 2009 |
Becker T, Kaiser A, Kunz H. Synthesis of dendrimeric tumor-associated mucin-type glycopeptide antigens Synthesis. 1113-1122. DOI: 10.1055/S-0028-1088002 |
0.304 |
|
| 2009 |
Westerlind U, Schröder H, Hobel A, Gaidzik N, Kaiser A, Niemeyer C, Schmitt E, Waldmann H, Kunz H. Cover Picture: Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity (Angew. Chem. Int. Ed. 44/2009) Angewandte Chemie International Edition. 48: 8151-8151. DOI: 10.1002/Anie.200904924 |
0.387 |
|
| 2009 |
Westerlind U, Schröder H, Hobel A, Gaidzik N, Kaiser A, Niemeyer C, Schmitt E, Waldmann H, Kunz H. Titelbild: Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity (Angew. Chem. 44/2009) Angewandte Chemie. 121: 8297-8297. DOI: 10.1002/Ange.200904924 |
0.385 |
|
| 2008 |
Erkel G, Belahmer H, Serwe A, Anke T, Kunz H, Kolshorn H, Liermann J, Opatz T. Oxacyclododecindione, a novel inhibitor of IL-4 signaling from Exserohilum rostratum. The Journal of Antibiotics. 61: 285-90. PMID 18653993 DOI: 10.1038/Ja.2008.40 |
0.368 |
|
| 2008 |
Madalinski M, Stoll M, Dietrich U, Kunz H. A selectively deprotectable 2,6-diaminogalactose scaffold for the solid-phase synthesis of potential RNA ligands Synthesis. 1106-1120. DOI: 10.1055/S-2008-1066982 |
0.306 |
|
| 2008 |
Erkel G, Belahmer H, Serwe A, Anke T, Kunz H, Kolshorn H, Liermann J, Opatz T. Oxacyclododecindione, a novel inhibitor of IL-4 signaling from Exserohilum rostratum Journal of Antibiotics. 61: 285-290. DOI: 10.1038/ja.2008.40 |
0.353 |
|
| 2007 |
Kranke B, Kunz H. Stereoselective syntheses of piperidinones and their modification by organometallic coupling reactions. Organic & Biomolecular Chemistry. 5: 349-54. PMID 17205180 DOI: 10.1039/B615113B |
0.36 |
|
| 2007 |
Herzner H, Kunz H. (p-Sulfomethyl)phenylalanine as a mimic of O-sulfatyl-tyrosine in synthetic partial sequences of P-Selectin glycoprotein ligand 1 (PSGL-1) Tetrahedron. 63: 6423-6436. DOI: 10.1016/J.Tet.2007.03.028 |
0.331 |
|
| 2006 |
Dziadek S, Griesinger C, Kunz H, Reinscheid UM. Synthesis and structural model of an alpha(2,6)-sialyl-t glycosylated MUC1 eicosapeptide under physiological conditions. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 4981-93. PMID 16642533 DOI: 10.1002/Chem.200600144 |
0.321 |
|
| 2006 |
Rösch A, Kunz H. Highly regioselective synthesis of a 3-O-sulfonated arabino Lewis(a) asparagine building block suitable for glycopeptide synthesis. Carbohydrate Research. 341: 1597-608. PMID 16584716 DOI: 10.1016/J.Carres.2006.03.003 |
0.307 |
|
| 2006 |
Klegraf E, Knauer S, Kunz H. Stereoselective synthesis of benzomorphan derivatives with perpivaloylated galactose as the chiral auxiliary. Angewandte Chemie (International Ed. in English). 45: 2623-6. PMID 16548042 DOI: 10.1002/Anie.200504090 |
0.371 |
|
| 2006 |
Kranke B, Kunz H. Stereoselective synthesis of chiral piperidine derivatives employing arabinopyranosylamine as the carbohydrate auxiliary Canadian Journal of Chemistry. 84: 625-641. DOI: 10.1139/V06-060 |
0.394 |
|
| 2006 |
Kunz H, Pfrengle W. Kohlenhydrate als chirale Matrices: Stereoselektive Tandem-Mannich-Michael-Reaktionen zur Synthese von Piperidin-Alkaloiden Angewandte Chemie. 101: 1041-1042. DOI: 10.1002/Ange.19891010811 |
0.313 |
|
| 2006 |
Kunz H, Barthels R. Der 2-(2-Pyridyl)ethoxycarbonyl-(Pyoc-)Rest - eine säure- und basestabile, hydrophile Schutzgruppe für die Aminofunktion bei der Peptidsynthese Angewandte Chemie. 95: 799-800. DOI: 10.1002/Ange.19830951011 |
0.32 |
|
| 2005 |
Pleuss N, Kunz H. N-glycosyl amides as glycosyl donors in stereoselective glycosylation reactions Synthesis. 122-130. DOI: 10.1055/S-2004-834911 |
0.322 |
|
| 2005 |
Knauer S, Kunz H. Palladium-catalysed C-C coupling reactions in the enantioselective synthesis of 2,4-disubstituted 4,5-dehydropiperidines using galactosylamine as a stereodifferentiating auxiliary Tetrahedron Asymmetry. 16: 529-539. DOI: 10.1016/J.Tetasy.2004.11.074 |
0.369 |
|
| 2005 |
Becker C, Hoben C, Schollmeyer D, Scherr G, Kunz H. Investigation of diketopiperazines containing a guanidino-functionalized sidechain as potential catalysts of enantioselective strecker reactions European Journal of Organic Chemistry. 1497-1499. DOI: 10.1002/Ejoc.200500044 |
0.334 |
|
| 2004 |
Dziadek S, Brocke C, Kunz H. Biomimetic synthesis of the tumor-associated (2,3)-sialyl-T antigen and its incorporation into glycopeptide antigens from the mucins MUC1 and MUC4. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 4150-62. PMID 15352098 DOI: 10.1002/Chem.200400228 |
0.319 |
|
| 2004 |
Zech G, Kunz H. Synthesis of a polymer-bound galactosylamine and its application as an immobilized chiral auxiliary in stereoselective syntheses of piperidine and amino acid derivatives. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 4136-49. PMID 15352097 DOI: 10.1002/Chem.200400253 |
0.387 |
|
| 2004 |
Knauer S, Kranke B, Krause L, Kunz H. Amino Sugars and Glycosylamines as Tools in Stereoselective Synthesis Current Organic Chemistry. 8: 1739-1761. DOI: 10.2174/1385272043369485 |
0.364 |
|
| 2004 |
Barth C, Seitz O, Kunz H. Synthese von 6-O-Benzylguanin und seinen Anker-Konjugaten / Synthesis of 6-O-Benzyl Guanine and its Conjugations with Linkers Zeitschrift FüR Naturforschung B. 59: 802-806. DOI: 10.1515/Znb-2004-0709 |
0.543 |
|
| 2004 |
Kranke B, Hebrault D, Schultz-Kukula M, Kunz H. Arabinosylamine in asymmetric syntheses of chiral piperidine alkaloids Synlett. 671-674. DOI: 10.1055/S-2004-817775 |
0.356 |
|
| 2004 |
Brocke C, Kunz H. Synthetic tumor-associated glycopeptide antigens from the tandem repeat sequence of the epithelial mucin MUC4 Synthesis. 525-542. DOI: 10.1055/S-2004-815962 |
0.327 |
|
| 2004 |
Opatz T, Kallus C, Wunberg T, Kunz H. Combinatorial synthesis of amino acid- and peptide-carbohydrate conjugates on solid phase Tetrahedron. 60: 8613-8626. DOI: 10.1016/J.Tet.2004.05.101 |
0.556 |
|
| 2004 |
Hünger U, Ohnsmann J, Kunz H. An vier Positionen in beliebiger Reihenfolge selektiv deblockierbare Kohlenhydratgerüste für die kombinatorische Synthese Angewandte Chemie. 116: 1125-1128. DOI: 10.1002/Ange.200352919 |
0.347 |
|
| 2003 |
Wagner M, Dziadek S, Kunz H. The (2-phenyl-2-trimethylsilyl)ethyl-(PTMSEL)-linker in the synthesis of glycopeptide partial structures of complex cell surface glycoproteins. Chemistry (Weinheim An Der Bergstrasse, Germany). 9: 6018-30. PMID 14679514 DOI: 10.1002/Chem.200305304 |
0.41 |
|
| 2003 |
Zech G, Kunz H. Stereoselective solid-phase synthesis of chiral piperidine derivatives by using an immobilized galactose auxiliary. Angewandte Chemie (International Ed. in English). 42: 787-90. PMID 12596200 DOI: 10.1002/Anie.200390208 |
0.35 |
|
| 2003 |
Dziadek S, Espinola CG, Kunz H. Synthetic glycopeptides for the development of antitumour vaccines Australian Journal of Chemistry. 56: 519-543. DOI: 10.1071/Ch02241 |
0.344 |
|
| 2003 |
Reipen T, Kunz H. Synthesis of Peptide and Glycopeptide Partial Structures of the Homophilic Recognition Domain of Epithelial Cadherin Synthesis. 2487-2502. DOI: 10.1055/S-2003-42429 |
0.348 |
|
| 2003 |
Brocke C, Kunz H. Synthetic Glycopeptides of the Tandem Repeat Sequence of the Epithelial Mucin MUC4 with Tumour-associated Carbohydrate Antigens Synlett. 2052-2056. DOI: 10.1055/S-2003-42029 |
0.309 |
|
| 2003 |
Opatz T, Kallus C, Wunberg T, Schmidt W, Henke S, Kunz H. D-glucose as a pentavalent chiral scaffold European Journal of Organic Chemistry. 1527-1536. DOI: 10.1002/Ejoc.200390211 |
0.539 |
|
| 2003 |
Opatz T, Kunz H. Book Review: Glycoscience Chemistry and Chemical Biology. Vols. I–III. Edited by Bertram Fraser-Reid, Kuniaki Tatsuta and Joachim Thiem Angewandte Chemie International Edition. 42: 22-22. DOI: 10.1002/Anie.200390044 |
0.435 |
|
| 2003 |
Opatz T, Kunz H. Buchbesprechung: Glycoscience Chemistry and Chemical Biology. Band I–III. Herausgegeben von Betram Fraser-Reid, Kuniaki Tatsuta und Joachim Thiem Angewandte Chemie. 115: 23-23. DOI: 10.1002/Ange.200390014 |
0.438 |
|
| 2002 |
Wagner M, Kunz H. The (2-Phenyl-2-trimethylsilyl)ethyl(PTMSEL) linker-A novel linker for the solid-phase synthesis of protected peptides and glycopeptides cleavable with fluoride. Angewandte Chemie (International Ed. in English). 41: 317-21. PMID 12491419 DOI: 10.1002/1521-3773(20020118)41:2<317::Aid-Anie317>3.0.Co;2-Y |
0.366 |
|
| 2002 |
Opatz T, Kallus C, Wunberg T, Schmidt W, Henke S, Kunz H. D-glucose as a multivalent chiral scaffold for combinatorial chemistry. Carbohydrate Research. 337: 2089-110. PMID 12433474 DOI: 10.1016/S0008-6215(02)00301-4 |
0.526 |
|
| 2002 |
Wagner M, Kunz H. Der (2-Phenyl-2-trimethylsilyl)ethyl-(PTMSE)-Ester – eine neutral spaltbare Carboxyschutzgruppe/The (2-Phenyl-2-trimethylsiylyl)ethyl (PTMSE) Ester – a Carboxy Protecting Group Cleavable under Neutral Conditions Zeitschrift FüR Naturforschung B. 57: 928-936. DOI: 10.1515/Znb-2002-0814 |
0.368 |
|
| 2002 |
Weymann M, Schulz-Kukula M, Knauer S, Kunz H. Carbohydrate Auxiliaries in Stereoselective Syntheses of Decahydroquinoline Alkaloids Monatshefte F?R Chemie / Chemical Monthly. 133: 571-587. DOI: 10.1007/978-3-7091-6130-2_16 |
0.342 |
|
| 2002 |
Wagner M, Kunz H. Der (2-Phenyl-2-trimethylsilyl)ethyl(PTMSEL)-Linker - ein neuer, mit Fluorid spaltbarer Anker für die Festphasensynthese von geschützten Peptiden und Glycopeptiden Angewandte Chemie. 114: 315-319. DOI: 10.1002/1521-3757(20020118)114:2<315::Aid-Ange315>3.0.Co;2-U |
0.318 |
|
| 2001 |
Follmann M, Rösch A, Klegraf E, Kunz H. Regio- and Stereoselective Addition of Grignard Reagents to N-Galactosyl-2-Pyridone: Synthesis of 4-Substituted 5,6-Didehydro-2-piperidinones Synlett. 2001: 1569-1570. DOI: 10.1055/S-2001-17460 |
0.373 |
|
| 2000 |
Herzner H, Reipen T, Schultz M, Kunz H. Synthesis of glycopeptides containing carbohydrate and Peptide recognition motifs. Chemical Reviews. 100: 4495-538. PMID 11749356 DOI: 10.1021/Cr990308C |
0.336 |
|
| 2000 |
Wagner M, Heiner S, Kunz H. The (2-Phenyl-2-trimethylsilyl)ethoxycarbonyl (Psoc) Group - A Novel Amino Protecting Group Synlett. 2000: 1753-1756. DOI: 10.1055/S-2000-8677 |
0.302 |
|
| 2000 |
Peilstöcker K, Kunz H. A Sialyl-Lewis A-Asparagine Building Block for Glycopeptide-Synthesis Synlett. 2000: 820-822. DOI: 10.1055/S-2000-6690 |
0.319 |
|
| 2000 |
Wagner M, Kunz H. (2-Phenyl-2-trimethylsilyl)ethyl (PTMSE) Esters - a Novel Carboxyl Protecting Group Synlett. 2000: 400-402. DOI: 10.1055/S-2000-6513 |
0.343 |
|
| 2000 |
Allef P, Kunz H. Glycosylation-induced asymmetric synthesis: β-amino acid esters via Mannich reactions Tetrahedron: Asymmetry. 11: 375-378. DOI: 10.1016/S0957-4166(99)00541-8 |
0.363 |
|
| 2000 |
Opatz T, Kunz H. A facile cleavage of allyl ethers on solid phase Tetrahedron Letters. 41: 10185-10188. DOI: 10.1016/S0040-4039(00)01835-9 |
0.513 |
|
| 2000 |
Dudziak G, Bézay N, Schwientek T, Clausen H, Kunz H, Liese A. Cyclodextrin-assisted Glycan Chain Extension on a Protected Glycosyl Amino Acid Tetrahedron. 56: 5865-5869. DOI: 10.1016/S0040-4020(00)00537-8 |
0.311 |
|
| 1999 |
Kunz H, Liebe B, Seitz O, Habermann J, Peilstöcker K, Sprengard U. Synthetic glycopeptides with tumor-associated antigen and cell adhesion ligand structure Collection of Czechoslovak Chemical Communications. 1: 134-146. DOI: 10.1135/Css199901134 |
0.487 |
|
| 1999 |
Kunz H. Synthetic glycopeptides and glycoproteins Collection of Czechoslovak Chemical Communications. 1: 67-78. DOI: 10.1135/Css199901067 |
0.308 |
|
| 1999 |
Löhr B, Orlich S, Kunz H. A Strategy Towards the Stereoselective Synthesis of 5-Hydroxylysine Synlett. 1999: 1139-1141. DOI: 10.1055/S-1999-2750 |
0.348 |
|
| 1999 |
Löhr B, Orlich S, Kunz H. Modified Trityl Ester Protecting Groups In Peptide Synthesis Synlett. 1999: 1136-1138. DOI: 10.1055/S-1999-2749 |
0.373 |
|
| 1999 |
Kallus C, Opatz T, Wunberg T, Schmidt W, Henke S, Kunz H. Combinatorial solid-phase synthesis using D-galactose as a chiral five-dimension-diversity scaffold Tetrahedron Letters. 40: 7783-7786. DOI: 10.1016/S0040-4039(99)01690-1 |
0.544 |
|
| 1998 |
Wunberg T, Kallus C, Opatz T, Henke S, Schmidt W, Kunz H. Carbohydrates as Multifunctional Chiral Scaffolds in Combinatorial Synthesis. Angewandte Chemie (International Ed. in English). 37: 2503-2505. PMID 29711363 DOI: 10.1002/(Sici)1521-3773(19981002)37:18<2503::Aid-Anie2503>3.0.Co;2-R |
0.552 |
|
| 1998 |
Asche G, Kunz H, Nar H, Köppen H, Briem H, Pook KH, Schiller PW, Chung NN, Lemieux C, Esser F. Synthesis of cyclic dipeptide templates, their incorporation into peptides and studies on their conformational and biological properties. The Journal of Peptide Research : Official Journal of the American Peptide Society. 51: 323-36. PMID 9606012 DOI: 10.1111/J.1399-3011.1998.Tb01223.X |
0.366 |
|
| 1998 |
Herzner H, Eberling J, Schultz M, Zimmer J, Kunz H. Oligosaccharide Synthesis via Electrophile-Induced Activation of Glycosyl-N-Allylcarbamates Journal of Carbohydrate Chemistry. 17: 759-776. DOI: 10.1080/07328309808002350 |
0.376 |
|
| 1998 |
Weymann M, Schultz-Kukula M, Kunz H. Auxiliary-controlled stereoselective enolate protonation: Enantioselective synthesis of cis and trans annulated decahydroquinoline alkaloids Tetrahedron Letters. 39: 7835-7838. DOI: 10.1016/S0040-4039(98)01745-6 |
0.32 |
|
| 1998 |
Habermann J, Kunz H. Fragment condensation on solid-phase in the synthesis of an amphiphilic glycopeptide from the homophilic recognition domain of epithelial cadherin 1 Tetrahedron Letters. 39: 4797-4800. DOI: 10.1016/S0040-4039(98)00923-X |
0.318 |
|
| 1998 |
Deloisy S, Kunz H. A novel synthesis of chain-extended amino sugar derivatives through aza-Cope rearrangement of N-galactosyl-N-homoallylamines Tetrahedron Letters. 39: 791-794. DOI: 10.1016/S0040-4039(97)10720-1 |
0.355 |
|
| 1998 |
Habermann J, Kunz H. Solid-phase synthesis of a glycopeptide from the homophilic recognition domain of epithelial cadherin 1 using a O-pentafluorophenyluronium salt Tetrahedron Letters. 39: 265-268. DOI: 10.1016/S0040-4039(97)10569-X |
0.321 |
|
| 1998 |
Leuck M, Kunz H. Synthesis of active principles from the leaves of Moringa oleifera using S-pent-4-enyl thioglycosides Carbohydrate Research. 312: 33-44. DOI: 10.1016/S0008-6215(98)00223-7 |
0.306 |
|
| 1998 |
Habermann J, Kunz H. Glycopeptide Synthesis UsingO-Pentafluorophenyluronium Salts as novel condensing reagents Journal F�R Praktische Chemie/Chemiker-Zeitung. 340: 233-239. DOI: 10.1002/Prac.19983400306 |
0.367 |
|
| 1998 |
Wunberg T, Kallus C, Opatz T, Henke S, Schmidt W, Kunz H. Carbohydrates as multifunctional chiral scaffolds in combinatorial synthesis Angewandte Chemie - International Edition. 37: 2503-2505. DOI: 10.1002/(SICI)1521-3773(19981002)37:18<2503::AID-ANIE2503>3.0.CO;2-R |
0.487 |
|
| 1998 |
Wunberg T, Kallus C, Opatz T, Henke S, Schmidt W, Kunz H. Kohlenhydrate – multifunktionelle chirale Gerüste in der kombinatorischen Synthese Angewandte Chemie. 110: 2620-2622. DOI: 10.1002/(Sici)1521-3757(19980918)110:18<2620::Aid-Ange2620>3.0.Co;2-R |
0.523 |
|
| 1997 |
Bröder W, Kunz H. Glycosyl azides as building blocks in convergent syntheses of oligomeric lactosamine and Lewis(x) saccharides. Bioorganic & Medicinal Chemistry. 5: 1-19. PMID 9043654 DOI: 10.1016/S0968-0896(96)00209-X |
0.346 |
|
| 1997 |
Seitz O, Kunz H. HYCRON, an Allylic Anchor for High-Efficiency Solid Phase Synthesis of Protected Peptides and Glycopeptides The Journal of Organic Chemistry. 62: 813-826. DOI: 10.1021/Jo960743W |
0.606 |
|
| 1997 |
Rück-Braun K, Stamm A, Engel S, Kunz H. β-Branched α-Halo Carboxylic Acid Derivatives via Stereoselective 1,4 Addition of Dialkylaluminum Chlorides to α,β-UnsaturatedN-Acyloxazolidinones The Journal of Organic Chemistry. 62: 967-975. DOI: 10.1021/Jo9520957 |
0.318 |
|
| 1997 |
Liebe B, Kunz H. Solid-Phase Synthesis of a Sialyl-Tn-Glycoundecapeptide of the MUC1 Repeating Unit Helvetica Chimica Acta. 80: 1473-1482. DOI: 10.1002/Hlca.19970800511 |
0.374 |
|
| 1997 |
Kunz H, Burgard A, Schanzenbach D. Asymmetric Mannich Synthesis ofβ-Amino Acids with Two New Stereogenic Centers at theα andβ Positions Angewandte Chemie International Edition in English. 36: 386-387. DOI: 10.1002/Anie.199703861 |
0.331 |
|
| 1995 |
Unverzagt C, Kunz H. Synthesis of glycopeptides and neoglycoproteins containing the fucosylated linkage region of N-glycoproteins. Bioorganic & Medicinal Chemistry. 2: 1189-201. PMID 7757416 DOI: 10.1016/S0968-0896(00)82070-2 |
0.392 |
|
| 1995 |
Hietter H, Schultz M, Kunz H. Solid-Phase Synthesis Of A 36 Amino Acid O-Fucosyl-Peptide With The Uncommon Thr-Fuc Linkage Synlett. 1995: 1219-1220. DOI: 10.1055/S-1995-5235 |
0.362 |
|
| 1995 |
Stahl W, Sprengard U, Kretzschmar G, Schmidt DW, Kunz H. Synthesis of Sulfated Lex-Trisaccharides Journal F�R Praktische Chemie/Chemiker-Zeitung. 337: 441-445. DOI: 10.1002/Prac.19953370196 |
0.351 |
|
| 1995 |
Biesalski H, Doepner G, Kunz H, Paust J, John M. Convenient Synthesis of Biologically Important Retinoids Liebigs Annalen. 1995: 717-720. DOI: 10.1002/Jlac.1995199504106 |
0.306 |
|
| 1995 |
Seitz O, Kunz H. A Novel Allylic Anchor for Solid-Phase Synthesis—Synthesis of Protected and Unprotected O-Glycosylated Mucin-Type Glycopeptides Angewandte Chemie International Edition in English. 34: 803-805. DOI: 10.1002/Anie.199508031 |
0.524 |
|
| 1995 |
Seitz O, Kunz H. Ein neuer allylischer Anker für die Festphasensynthese – Synthese von geschützten und ungeschütztenO-Glycopeptiden des Mucintyps Angewandte Chemie. 107: 901-904. DOI: 10.1002/Ange.19951070726 |
0.526 |
|
| 1994 |
Bröder W, Kunz H. A new method of anomeric protection and activation based on the conversion of glycosyl azides into glycosyl fluorides. Carbohydrate Research. 249: 221-41. PMID 8252554 DOI: 10.1016/0008-6215(93)84071-D |
0.343 |
|
| 1994 |
Ganz I, Kunz H. Carbohydrates as Chiral Auxiliaries. [2+2) Cycloadditions of Ketenes to Enol Ethers Synthesis. 1994: 1353-1358. DOI: 10.1055/S-1994-25693 |
0.326 |
|
| 1994 |
Liebe B, Kunz H. Synthesis of sialyl-Tn antigen. Regioselective sialylation of a galactosamine threonine conjugate unblocked in the carbohydrate portion Tetrahedron Letters. 35: 8777-8778. DOI: 10.1016/S0040-4039(00)78495-4 |
0.354 |
|
| 1994 |
Kosch W, März J, Kunz H. Synthesis of glycopeptide derivatives of Peptide T on a solid phase using an allylic linkage Reactive Polymers. 22: 181-194. DOI: 10.1016/0923-1137(94)90116-3 |
0.374 |
|
| 1994 |
Stahl W, Sprengard U, Kretzschmar G, Kunz H. Synthesis of Deoxy Sialyl Lewisx Analogues, Potential Selectin Antagonists Angewandte Chemie International Edition in English. 33: 2096-2098. DOI: 10.1002/Anie.199420961 |
0.34 |
|
| 1994 |
Stahl W, Sprengard U, Kretzschmar G, Kunz H. Synthese von Desoxy-Sialyl-Lewisx-Analoga, potentiellen Selectin-Antagonisten Angewandte Chemie. 106: 2186-2188. DOI: 10.1002/Ange.19941062025 |
0.344 |
|
| 1993 |
Braun P, Waldmann H, Kunz H. Chemoenzymatic synthesis of O-glycopeptides carrying the tumor associated TN-antigen structure. Bioorganic & Medicinal Chemistry. 1: 197-207. PMID 8081853 DOI: 10.1016/S0968-0896(00)82122-7 |
0.478 |
|
| 1993 |
Kunz H. Glycopeptides of biological interest: A challenge for chemical synthesis Pure and Applied Chemistry. 65: 1223-1232. DOI: 10.1351/Pac199365061223 |
0.351 |
|
| 1993 |
Rück K, Kunz H. Stereoselective Conjugate Addition of Organoaluminum Chlorides to α,β-Unsaturated Carboxylic Acid Derivatives Synthesis. 1993: 1018-1028. DOI: 10.1055/S-1993-25990 |
0.331 |
|
| 1993 |
Schultz M, Kunz H. Synthetic O-glycopeptides as model substrates for glycosyltransferases Tetrahedron: Asymmetry. 4: 1205-1220. DOI: 10.1016/S0957-4166(00)80230-X |
0.321 |
|
| 1993 |
Braum G, Braun P, Kowalczyk D, Kunz H. Enzymatische hydrolyse hydrophiler ester durch lipasen - eine milde carboxydeblockierung von peptiden und glycopeptiden Tetrahedron Letters. 34: 3111-3114. DOI: 10.1016/S0040-4039(00)93392-6 |
0.329 |
|
| 1993 |
Kunz H, Zimmer J. Glycoside synthesis via electrophile-induced activation of N-allyl carbamates Tetrahedron Letters. 34: 2907-2910. DOI: 10.1016/S0040-4039(00)60478-1 |
0.344 |
|
| 1993 |
Kunz H, Rück K. Carbohydrates as Chiral Auxiliaries in Stereoselective Synthesis. New Synthetic Methods (90) Angewandte Chemie. 32: 336-358. DOI: 10.1002/Anie.199303361 |
0.339 |
|
| 1993 |
Kunz H, Rück K. Kohlenhydrate als chirale Auxiliare in der stereoselektiven Synthese Angewandte Chemie. 105: 355-377. DOI: 10.1002/Ange.19931050305 |
0.321 |
|
| 1992 |
Kunz H, Brill WK-, 秀樹 石. Synthesis of Biologically Interesting Glycopeptides Trends in Glycoscience and Glycotechnology. 4: 71-82. DOI: 10.4052/Tigg.4.71 |
0.36 |
|
| 1992 |
Laschat S, Kunz H. Carbohydrates as Chiral Templates: Stereoselective Synthesis of (R)- and (S)-α-Aminophosphonic Acid Derivatives Synthesis. 1992: 90-95. DOI: 10.1055/S-1992-34155 |
0.359 |
|
| 1992 |
Rück K, Kunz H. A Bicyclic Carbohydrate Oxazolidinone Template for Stereoselective 1,4-Additions of Organoaluminium Chlorides to Unsaturated Carboxylic Acid Derivatives Synlett. 1992: 343-344. DOI: 10.1055/S-1992-22008 |
0.34 |
|
| 1992 |
Kunz H, März J. Synthesis of Glycopeptides with Lewisa Antigen Side Chain and HIV Peptide T Sequence Using the Trichloroethoxycarbonyl/Allyl Ester Protecting Group Combination Synlett. 1992: 591-593. DOI: 10.1055/S-1992-21427 |
0.329 |
|
| 1992 |
März J, Kunz H. Synthesis of Selectively Deprotectable Asparagine Glycoconjugates with a LewisaAntigen Side Chain Synlett. 1992: 589-590. DOI: 10.1055/S-1992-21426 |
0.312 |
|
| 1992 |
Braun P, Waldmann H, Kunz H. Selective Enzymatic Removal of Protecting Functions: Heptyl Esters as Carboxy Protecting Groups in Glycopeptide Synthesis Synlett. 1992: 39-40. DOI: 10.1055/S-1992-21258 |
0.488 |
|
| 1992 |
Schultz M, Hermann P, Kunz H. Enzymatic cleavage of tert butyl esters thermitase catalyzed deprotection of peptides and o glycopeptides Synlett. 1992: 37-38. DOI: 10.1055/S-1992-21257 |
0.345 |
|
| 1992 |
Schultz M, Kunz H. Enzymatic glycosylation of o-glycopeptides Tetrahedron Letters. 33: 5319-5322. DOI: 10.1016/S0040-4039(00)79082-4 |
0.305 |
|
| 1992 |
Kunz H, Kullmann R. Metal ion-promoted activation of amino acid esters of carbohydrates in the synthesis of peptides Tetrahedron Letters. 33: 6115-6118. DOI: 10.1016/S0040-4039(00)60020-5 |
0.325 |
|
| 1992 |
Kunz H, Kullmann R, Wernig P, Zimmer J. Stereoselective Synthesis of β-1-O-Acyl Derivatives of Carbohydrates: An Application of the Cesium Effect. Tetrahedron Letters. 33: 1969-1972. DOI: 10.1016/0040-4039(92)88116-M |
0.362 |
|
| 1992 |
Unverzagt C, Kunz H. Stereoselective synthesis of glycosides and anomeric azides of glucosamine Journal F�R Praktische Chemie/Chemiker-Zeitung. 334: 570-578. DOI: 10.1002/Prac.19923340705 |
0.375 |
|
| 1991 |
Waldmann H, Braun P, Kunz H. New enzymatic protecting group techniques for the construction of peptides and glycopeptides. Biomedica Biochimica Acta. 50: S243-8. PMID 1820053 |
0.417 |
|
| 1991 |
Kunz H, Pfrengle W, Rück K, Sager W. Stereoselective Synthesis of L-Amino Acids via Strecker and Ugi Reaktions on Carbohydrate Templates Synthesis. 1991: 1039-1042. DOI: 10.1055/S-1991-26641 |
0.359 |
|
| 1991 |
Ciommer M, Kunz H. Synthesis of Glycopeptides with Partial Structure of Human Glycophorin Using the Fluorenylmethoxycarbonyl/ Allyl Ester Protecting Group Combination Synlett. 1991: 593-595. DOI: 10.1055/S-1991-20810 |
0.343 |
|
| 1991 |
Stähle W, Kunz H. Carbohydrates as Chiral Templates: Stereoselective Diels-Alder Synthesis with Dienes of Differing Reactivity Synlett. 1991: 260-262. DOI: 10.1055/S-1991-20700 |
0.368 |
|
| 1991 |
Braun P, Waldmann H, Vogt W, Kunz H. Selektive enzymatische Schutzgruppenabspaltungen: Der n-Heptylester als Carboxylschutzgruppe in der Peptidsynthese Liebigs Annalen Der Chemie. 1991: 165-170. DOI: 10.1002/Jlac.199119910130 |
0.516 |
|
| 1991 |
Kunz H, Sager W, Schanzenbach D, Decker M. Carbohydrates as chiral templates: Stereoselective Strecker synthesis of D‐α‐amino nitriles and acids using O‐pivaloylated D‐galactosylamine as the auxiliary European Journal of Organic Chemistry. 1991: 649-654. DOI: 10.1002/Jlac.1991199101117 |
0.36 |
|
| 1990 |
Kunz H, Wernig P, Schilling M, März J, Unverzagt C, Birnbach S, Lang U, Waldmann H. Synthetic tumor-associated glycopeptide antigens. Environmental Health Perspectives. 88: 247-9. PMID 2272318 DOI: 10.2307/3431084 |
0.446 |
|
| 1990 |
Kunz H, Birnbach S, Wernig P. Synthesis of glycopeptides with the TN and T antigen structures, and their coupling to bovine serum albumin. Carbohydrate Research. 202: 207-23. PMID 2224891 DOI: 10.1016/0008-6215(90)84081-5 |
0.343 |
|
| 1990 |
Waldmann H, März J, Kunz H. Synthesis of 2-acetamido-2-deoxyglucosylasparagine glyco-tripeptides and -pentapeptides by selective C- and N-terminal elongation of the peptide chain. Carbohydrate Research. 196: 75-93. PMID 2161285 DOI: 10.1016/0008-6215(90)84107-6 |
0.533 |
|
| 1990 |
Kunz H, Wernig P, Schultz M. A New Activating Principle in Glycoside Synthesis Based on Electrophile-Induced Lactonization of Glucosyl 4-Pentenoates Synlett. 1990: 631-632. DOI: 10.1055/S-1990-21193 |
0.308 |
|
| 1990 |
Laschat S, Kunz H. Carbohydrates as Chiral Templates: Stereoselective Synthesis of (R)-Homoallyl Amines Using L-Fucose as the Auxiliary Formally Enantiomeric to D-Galactose Synlett. 1990: 629-630. DOI: 10.1055/S-1990-21192 |
0.354 |
|
| 1990 |
Bröder W, Kunz H. Glycoside and Saccharide Synthesis UsingN-Glycosyl Triazoles as Hydrolytically Stable Glycosyl Donors Synlett. 1990: 251-252. DOI: 10.1055/S-1990-21051 |
0.339 |
|
| 1990 |
Braun P, Waldmann H, Vogt W, Kunz H. Selective Enzymatic Removal of Protecting Functions: Heptyl Esters as Carboxy Protecting Groups in Peptide Synthesis Synlett. 1990: 105-107. DOI: 10.1055/S-1990-21002 |
0.502 |
|
| 1990 |
Laschat S, Kunz H. Carbohydrates as Chiral Templates: Stereoselective Synthesis of Chiral Homoallyl Amines and β-Amino Acids Synlett. 1990: 51-52. DOI: 10.1055/S-1990-20985 |
0.364 |
|
| 1990 |
Unverzagt C, Kunz H, Paulson JC. High-efficiency synthesis of sialyloligosaccharides and sialoglycopeptides Journal of the American Chemical Society. 112: 9308-9309. DOI: 10.1021/Ja00181A037 |
0.316 |
|
| 1990 |
Schultz M, Waldmann H, Vogt W, Kunz H. Stereospecific CC-bond formation with rabbit muscle aldolase - A chemoenzymatic synthesis of (+)-exo-brevicomin Tetrahedron Letters. 31: 867-868. DOI: 10.1016/S0040-4039(00)94649-5 |
0.43 |
|
| 1990 |
Schultz M, Waldmann H, Kunz H, Vogt W. Chemoenzymatische „Chiral-Pool”-Synthese von (+)-exo-Brevicomin aus Kohlenhydraten mit Fructose-1,6-diphosphat-Aldolase Liebigs Annalen Der Chemie. 1990: 1019-1024. DOI: 10.1002/Jlac.1990199001184 |
0.496 |
|
| 1989 |
Pfrengle W, Kunz H. Hetero-Diels-Alder reactions on a carbohydrate template: stereoselective synthesis of (S)-anabasin The Journal of Organic Chemistry. 54: 4261-4263. DOI: 10.1021/Jo00279A001 |
0.318 |
|
| 1989 |
Friedrich-Bochnitschek S, Waldmann H, Kunz H. Allyl esters as carboxy protecting groups in the synthesis of O-glycopeptides The Journal of Organic Chemistry. 54: 751-756. DOI: 10.1021/Jo00265A007 |
0.499 |
|
| 1989 |
Kunz H, Pfrengle W, Sager W. Carbohydrates as chiral templates: Diastereoselective Ugi synthesis of (S)-amino acids using O-acylated D-arabinopyranosylamine as the auxiliary Tetrahedron Letters. 30: 4109-4110. DOI: 10.1016/S0040-4039(00)99334-1 |
0.369 |
|
| 1989 |
Kunz H, Waldmann H, März J. Synthese vonN-Glycopeptid-Partialstrukturen der Verknüpfungsregion sowohl der Transmembran-Neuraminidase eines Influenza-Virus als auch des Faktors B des menschlichen Komplementsystems Liebigs Annalen Der Chemie. 1989: 45-49. DOI: 10.1002/Jlac.198919890110 |
0.439 |
|
| 1989 |
Kunz H, Schanzenbach D. Carbohydrates as Chiral Templates: Stereoselective Synthesis of ?-Amino Acids Angewandte Chemie International Edition in English. 28: 1068-1069. DOI: 10.1002/Anie.198910681 |
0.357 |
|
| 1989 |
Kunz H, Pfrengle W. Carbohydrates as Chiral Templates: Stereoselective Tandem Mannich-Michael Reactions for the Synthesis of Piperidine Alkaloids Angewandte Chemie International Edition in English. 28: 1067-1068. DOI: 10.1002/Anie.198910671 |
0.358 |
|
| 1988 |
Waldmann H, Kunz H. 1,3-Dithian-2-ylmethyl esters as two-step carboxy-protecting groups in the synthesis of N-glycopeptides The Journal of Organic Chemistry. 53: 4172-4175. DOI: 10.1021/Jo00253A003 |
0.485 |
|
| 1988 |
Kunz H, Pfrengle W. Asymmetric synthesis on carbohydrate templates: stereoselective Ugi-synthesis of .alpha.-amino acid derivatives Journal of the American Chemical Society. 110: 651-652. DOI: 10.1021/Ja00210A084 |
0.369 |
|
| 1988 |
Kunz H, Sager W, Pfrengle W, Schanzenbach D. Reversal of asymmetric induction in stereoselective strecker synthesis on galactosyl amine as the chiral matrix Tetrahedron Letters. 29: 4397-4400. DOI: 10.1016/S0040-4039(00)80504-3 |
0.39 |
|
| 1988 |
Kunz H, Pfrengle W. Carbohydrates as chiral templates: asymmetric ugi-synthesis of alpha-amino acids using galactosylamines as the chiral matrices Tetrahedron. 44: 5487-5494. DOI: 10.1016/S0040-4020(01)86054-3 |
0.354 |
|
| 1988 |
Kunz H, Waldmann H, Klinkhammer U. The Allyl Ester as Carboxy-Protecting Group in the Stereoselective Construction of Neuraminic-Acid Glycosides Helvetica Chimica Acta. 71: 1868-1874. DOI: 10.1002/Hlca.19880710804 |
0.474 |
|
| 1988 |
Kunz H, Unverzagt C. Protecting-Group-Dependent Stability of Intersaccharide Bonds?Synthesis of a Fucosyl-Chitobiose Glycopeptide Angewandte Chemie International Edition in English. 27: 1697-1699. DOI: 10.1002/Anie.198816971 |
0.312 |
|
| 1988 |
Kunz H, März J. Thep-Nitrocinnamyloxycarbonyl(Noc) Moiety—an Acid-stable Amino-protecting Group Removable under Neutral Conditions for Peptide and Glycopeptide Synthesis Angewandte Chemie International Edition in English. 27: 1375-1377. DOI: 10.1002/Anie.198813751 |
0.367 |
|
| 1988 |
Kunz H, Dombo B. Solid Phase Synthesis of Peptides and Glycopeptides on Polymeric Supports with Allylic Anchor Groups Angewandte Chemie International Edition in English. 27: 711-713. DOI: 10.1002/Anie.198807111 |
0.351 |
|
| 1988 |
Kunz H, Unverzagt C. Schutzgruppenabhängige Stabilität von Intersaccharid-Bindungen – Synthese eines Fucosyl-Chitobiose-Glycopeptids Angewandte Chemie. 100: 1763-1765. DOI: 10.1002/Ange.19881001212 |
0.304 |
|
| 1988 |
Kunz H, Dombo B. Festphasen-Synthese von Peptiden und Glycopeptiden an polymeren Trägern mit allylischen Ankergruppen Angewandte Chemie. 100: 732-734. DOI: 10.1002/Ange.19881000528 |
0.344 |
|
| 1987 |
Kunz H, Lerchen H. Stereocontrolled synthesis of D-α-hydroxy carboxylic acid from L-amino acids Tetrahedron Letters. 28: 1873-1876. DOI: 10.1016/S0040-4039(00)95997-5 |
0.317 |
|
| 1987 |
Kunz H, Müller B, Weissmüller J. Stereoselective synthesis of C-glycosyl compounds via Michael addition of trimethylsilyl enol ethers and enamines to hex-1-enopyran-3-uloses Carbohydrate Research. 171: 25-34. DOI: 10.1016/S0008-6215(00)90876-0 |
0.346 |
|
| 1987 |
Kunz H, Sager W. Diastereoselective Strecker Synthesis of α-Aminonitriles on Carbohydrate Templates Angewandte Chemie International Edition in English. 26: 557-559. DOI: 10.1002/Anie.198705571 |
0.331 |
|
| 1987 |
Kunz H. Synthese von Glycopeptiden, Partialstrukturen biologischer Erkennungskomponenten Angewandte Chemie. 99: 297-311. DOI: 10.1002/Ange.19870990405 |
0.321 |
|
| 1986 |
Kunz H, Pfrengle W. Effective 1,2-trans-glycosylation of complex alcohols and phenols using the oximate orthoester of O-pivaloyl glucopyranose Journal of the Chemical Society, Chemical Communications. 713-714. DOI: 10.1039/C39860000713 |
0.303 |
|
| 1986 |
Harreus A, Kunz H. 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 Liebigs Annalen Der Chemie. 1986: 717-730. DOI: 10.1002/Jlac.198619860411 |
0.306 |
|
| 1986 |
KUNZ H, WALDMANN H. ChemInform Abstract: Construction of Disaccharidic N-Glycopeptides. Synthesis of the Transmembrane Neuraminidase Binding Site of Influenza Virus. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198603323 |
0.325 |
|
| 1986 |
Kunz H, Birnbach S. Synthese von O-Glycopeptiden des tumorassoziierten TN- und T-Antigen-Typs und deren Anknüpfung an Rinderserumalbumin Angewandte Chemie. 98: 354-355. DOI: 10.1002/Ange.19860980419 |
0.3 |
|
| 1985 |
Kunz H, Waldmann H. 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 Journal of the Chemical Society, Chemical Communications. 638-640. DOI: 10.1039/C39850000638 |
0.489 |
|
| 1985 |
Lerchen H, Kunz H. Stereoselektive synthese von D-α-hydroxycarbonsäuren bzw. D-α-hydroxycarbonsäuren enthaltenden depsipeptiden aus L-aminosäuren Tetrahedron Letters. 26: 5257-5260. DOI: 10.1016/S0040-4039(00)95009-3 |
0.331 |
|
| 1985 |
Kunz H, Schaumlöffel G. Die 2-(Triphenylphosphonio)isopropyloxycarbonyl-(Ppoc-)-Gruppe und am Phosphoniumzentrum modizifierte analoge Reste als Aminoschutzgruppen bei der Peptidsynthese European Journal of Organic Chemistry. 1985: 1784-1793. DOI: 10.1002/Jlac.198519850906 |
0.379 |
|
| 1985 |
Kunz H, Waldmann H. Synthesis of the Glycopeptide Partial Sequence A80-A84 of Human Fibroblast Interferon Helvetica Chimica Acta. 68: 618-622. DOI: 10.1002/Chin.198535293 |
0.391 |
|
| 1985 |
Kunz H, Waldmann H. Construction of DisaccharideN-Glycopeptides?Synthesis of the Linkage Region of the Transmembrance-Neuraminidase of an Influenza Virus Angewandte Chemie International Edition in English. 24: 883-885. DOI: 10.1002/Anie.198508831 |
0.398 |
|
| 1985 |
Kunz H, Waldmann H. Aufbau disaccharidischerN-Glycopeptide – Synthese der Verknüpfungsregion der Transmembran-Neuraminidase eines Influenza-Virus Angewandte Chemie. 97: 885-887. DOI: 10.1002/Ange.19850971033 |
0.456 |
|
| 1984 |
Kunz H, Weiβmüller J, Müller B. Stereoselektive c-glycosidsynthese durch titan-(iv)-katalysierte addition von silylenolethern an 2-acyloxy-3-keto-glycale Tetrahedron Letters. 25: 3571-3574. DOI: 10.1016/S0040-4039(01)91078-0 |
0.315 |
|
| 1984 |
Kunz H, Birnbach S. Der 2-(4-pyridyl)Ethoxycarbonyl-(4-Pyoc)-rest - eine hydrophile, säure- und basenstabile aminoschutzgruppe für die peptidsynthese Tetrahedron Letters. 25: 3567-3570. DOI: 10.1016/S0040-4039(01)91077-9 |
0.376 |
|
| 1984 |
Kunz H. Synthese von Glycopeptiden Nachrichten Aus Chemie, Technik Und Laboratorium. 32: 11-16. DOI: 10.1002/Nadc.19840320105 |
0.349 |
|
| 1984 |
Kunz H, Weißmüller J. Synthese des Methylethers der Herzgift-Methylreduktinsäure ausD-Glucose Liebigs Annalen Der Chemie. 1984: 66-77. DOI: 10.1002/Jlac.198419840108 |
0.305 |
|
| 1984 |
KUNZ H, WALDMANN H. ChemInform Abstract: ALLYL GROUPS AS MILD AND SELECTIVE CLEAVABLE CARBOXY PROTECTIVE GROUPS FOR THE SYNTHESIS OF SENSITIVE O-GLYCOPEPTIDES Chemischer Informationsdienst. 15. DOI: 10.1002/chin.198415343 |
0.411 |
|
| 1984 |
WALDMANN H, KUNZ H. ChemInform Abstract: ALLYL ESTERS AS SELECTIVELY REMOVABLE CARBOXY-PROTECTING FUNCTIONS IN PEPTIDE AND N-GLYCOPEPTIDE SYNTHESES Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198402318 |
0.422 |
|
| 1984 |
Kunz H, Kneip M. 2-(Pyridyl)ethyl Esters as Secure yet Readily Removable Polarophilic Carboxy-Protection in Peptide Synthesis Angewandte Chemie International Edition in English. 23: 716-717. DOI: 10.1002/Anie.198407161 |
0.352 |
|
| 1984 |
Kunz H, Unverzagt C. The Allyloxycarbonyl (Aloc) Moiety?Conversion of an Unsuitable into a Valuable Amino Protecting Group for Peptide Synthesis Angewandte Chemie International Edition in English. 23: 436-437. DOI: 10.1002/Anie.198404361 |
0.379 |
|
| 1984 |
Kunz H, Waldmann H. The Allyl Group as Mildly and Selectively Removable Carboxy-Protecting Group for the Synthesis of LabileO-Glycopeptides Angewandte Chemie International Edition in English. 23: 71-72. DOI: 10.1002/Anie.198400711 |
0.468 |
|
| 1984 |
Kunz H, Unverzagt C. Der Allyloxycarbonyl(aloc)-Rest – die Verwandlung einer untauglichen in eine wertvolle Aminoschutzgruppe für die Peptidsynthese Angewandte Chemie. 96: 426-427. DOI: 10.1002/Ange.19840960612 |
0.31 |
|
| 1984 |
Kunz H, Waldmann H. Die Allylgruppe als mild und selektiv abspaltbare Carboxy-Schutzgruppe zur Synthese empfindlicherO-Glycopeptide Angewandte Chemie. 96: 49-50. DOI: 10.1002/Ange.19840960108 |
0.428 |
|
| 1983 |
Buchholz M, Kunz H. Synthese von Giycopeptiden: Selektive C-terminale Deblockierung und Peptidkettenverlängerung an Glucosylserin-Derivaten Liebigs Annalen Der Chemie. 1983: 1859-1885. DOI: 10.1002/Jlac.198319831103 |
0.387 |
|
| 1983 |
Waldmann H, Kunz H. Allylester als selektiv abspaltbare Carboxyschutzgruppen in der Peptid- undN-Glycopeptidsynthese Liebigs Annalen Der Chemie. 1983: 1712-1725. DOI: 10.1002/Jlac.198319831007 |
0.503 |
|
| 1983 |
Kauth H, Kunz H. Synthese von geschützten Serin-Glycopeptiden durch N-terminale Peptidketten-Verlängerung Liebigs Annalen Der Chemie. 1983: 360-366. DOI: 10.1002/Jlac.198319830303 |
0.358 |
|
| 1983 |
Kunz H, Kauth H. Synthese von geschützten Asparagin-Glycopeptiden durch N-terminale Peptidketten- Verlängerung. _ Teilsequenzen der Rinder-Desoxyribonuclease A und des luteinisierenden Hormons Liebigs Annalen Der Chemie. 1983: 337-359. DOI: 10.1002/Jlac.198319830302 |
0.335 |
|
| 1983 |
Kunz H, Barthels R. The 2-(2-Pyridyl)ethoxycarbonyl-(Pyoc) Residue?An Acid- and Base-Stable, Hydrophilic Protecting Group for the Amino Function in Peptide Synthesis Angewandte Chemie International Edition in English. 22: 783-784. DOI: 10.1002/Chin.198406317 |
0.367 |
|
| 1983 |
KUNZ H, WALDMANN H. ChemInform Abstract: 1,3-DITHIAN-2-YLMETHYL ESTER AS INTERMEDIATE PROTECTIVE GROUPS FOR CARBOXYL FUNCTION IN PEPTIDE SYNTHESIS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198315335 |
0.446 |
|
| 1983 |
Kunz H, Waldmann H. 1,3-Dithian-2-yl Methyl Ester as Two-Step Protecting Group for the Carboxy Function in Peptide Synthesis Angewandte Chemie International Edition in English. 22: 62-62. DOI: 10.1002/Anie.198300621 |
0.499 |
|
| 1983 |
Kunz H, Waldmann H. 1,3‐Dithian‐2‐yl‐methylester als Zweistufen‐Schutzgruppe für die Carboxyfunktion bei der Peptidsynthese Angewandte Chemie. 95: 47-48. DOI: 10.1002/Ange.19830950108 |
0.385 |
|
| 1982 |
Kunz H, Bechtolsheimer H. Synthese sterisch gehinderter Peptide und Depsipeptide nach einem Säurechlorid-Verfahren mit 2-Phosphonioethoxycarbonyl-(Peoc-)Aminosäuren und -Hydroxysäuren Liebigs Annalen Der Chemie. 1982: 2068-2078. DOI: 10.1002/Jlac.198219821113 |
0.33 |
|
| 1982 |
Kunz H, Schmidt P. Synthese und Reaktionen der 3-O-Phosphoniogluco-und -allofuranosen Liebigs Annalen Der Chemie. 1982: 1245-1260. DOI: 10.1002/Jlac.198219820703 |
0.359 |
|
| 1982 |
Kunz H, Harreus A. Glycosidsynthese mit 2,3,4,6-Tetra-O-pivaloyl-α-D-glucopyrancsylbromid Liebigs Annalen Der Chemie. 1982: 41-48. DOI: 10.1002/Jlac.198219820105 |
0.319 |
|
| 1982 |
Barthels R, Kunz H. The 1,3-Dithian-2-Yl-Methoxycarbonyl (Dmoc-) Radical, A Protective Group For The Amino Function In Peptide Synthesis Cheminform. 13. DOI: 10.1002/Chin.198228308 |
0.363 |
|
| 1982 |
KUNZ H, BARTHELS R. ChemInform Abstract: THE 1,3-DITHIAN-2-YLMETHOXYCARBONYL (DMOC) GROUP AS A TWO-STEP AMINO PROTECTIVE FUNCTION FOR AMINO ACIDS AND PEPTIDES Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198223346 |
0.35 |
|
| 1982 |
Kunz H, Barthels R. Der 1,3-Dithian-2-ylmethoxycarbonyl-(Dmoc)-Rest als Zweistufen-Schutzgruppe für die Aminofunktion von Aminosäuren und Peptiden Chemische Berichte. 115: 833-845. DOI: 10.1002/Cber.19821150302 |
0.344 |
|
| 1982 |
Barthels R, Kunz H. Der 1,3-Dithian-2-yl-methoxycarbonyl-(Dmoc-) Rest, eine Sicherheitsschutzgruppe f�r die Aminofunktion bei der Peptid-syntheses Angewandte Chemie International Edition in English. 21: 702-710. DOI: 10.1002/Anie.198207020 |
0.302 |
|
| 1982 |
Barthels R, Kunz H. The 1,3-Dithian-2-ylmethoxycarbonyl (Dmoc) Moiety-A Protecting Group for the Amino Function in Peptide Synthesis Angewandte Chemie International Edition in English. 21: 292-292. DOI: 10.1002/Anie.198202921 |
0.355 |
|
| 1981 |
Kunz H, Kauth H. Synthesis of Glycopeptides: Selective Amino‐Deblocking of 2‐Phosphonioethoxycarbonyl‐Protected Asparagine N‐Acetylglucosamine Moieties Angewandte Chemie. 20: 895-896. DOI: 10.1002/Anie.198108951 |
0.343 |
|
| 1981 |
Kunz H, Buchholz M. Synthesis of Glycopeptides: Selective Carboxy-Deblocking of Completely Protected Glucosylserine Derivatives Angewandte Chemie International Edition in English. 20: 894-895. DOI: 10.1002/Anie.198108941 |
0.364 |
|
| 1981 |
Kunz H, Buchholz M. Synthese von Glycopeptiden: Selektive Carboxydeblockierung an vollständig geschützten Glucosylserin-Derivaten Angewandte Chemie. 93: 917-918. DOI: 10.1002/Ange.19810931027 |
0.349 |
|
| 1979 |
Kunz H, Kauth H. Synthese und Reaktionen von Phosphonio-acetyl-Peptiden und ihren Yliden / Synthesis and Reactions of Phosphonio-acetyl Peptides and Ylides Zeitschrift FüR Naturforschung B. 34: 1737-1744. DOI: 10.1515/Znb-1979-1222 |
0.371 |
|
| 1979 |
Bartheis R, Kunz H. Modifikation der N-terminalen 2-Methylthio-ethoxycarbonyl-(Mtc)-Sehutzgruppe von Peptiden mit Bromcyan / Modification of the N-Terminal 2-Methylthioethoxycarbonyl Protective Function of Peptides Using Cyanogen Bromide Zeitschrift FüR Naturforschung B. 34: 1121-1123. DOI: 10.1515/Znb-1979-0816 |
0.345 |
|
| 1979 |
Kunz H, Schmidt P. Eine neue synthese for 3-desoxy-3-iod-zucker über alkoxyphosphoniumsalze Tetrahedron Letters. 20: 2123-2124. DOI: 10.1016/S0040-4039(01)86279-1 |
0.331 |
|
| 1979 |
Bechtolsheimer H, Buchholz M, Kunz H. Die Reaktion von 2-Halogenethoxycarbonyl-Verbindungen mit tertiären Phosphanen Liebigs Annalen Der Chemie. 1979: 1908-1914. DOI: 10.1002/Jlac.197919791127 |
0.374 |
|
| 1979 |
BARTHELS R, KUNZ H. ChemInform Abstract: MODIFICATION OF THE N-TERMINAL 2-METHYLTHIOETHOXYCARBONYL (MTC) PROTECTING GROUP OF PEPTIDES USING CYANOGEN BROMIDE Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197948347 |
0.334 |
|
| 1979 |
HORNER L, WALACH P, KUNZ H. ChemInform Abstract: ORGANOPHOSPHORUS COMPOUNDS, 87. SYNTHESIS AND REACTIONS OF CYCLIC PHOSPHONIUM SALTS WITH 2 PHOSPHORUS ATOMS IN 7,8,9,10 AND 11 RINGS AND 4 PHOSPHORUS ATOMS IN 16,18 AND 20 RINGS Chemischer Informationsdienst. 10. DOI: 10.1002/Chin.197923240 |
0.503 |
|
| 1979 |
Kunz H, Schmidt P. Veresterung und Veretherung sterisch gehinderter Kohlenhydrat-Hydroxylfunktionen mit dem System Triphenylphosphan/Azodicarbonsäureester Chemische Berichte. 112: 3886-3894. DOI: 10.1002/Cber.19791121213 |
0.335 |
|
| 1979 |
Kunz H, Buchholz M. Das System 2-Halogenethylester/Cholinester als Zweistufen-Schutzgruppe für die Carboxylfunktion von Aminosäuren und Peptiden Chemische Berichte. 112: 2145-2157. DOI: 10.1002/Cber.19791120622 |
0.373 |
|
| 1978 |
Kunz H, Schmidt P. Die ungewöhnliche Reaktion von 1.2—5.6-Di-O-isopropyliden-α-D-glucofuranose (Diacetonglucose) mit dem System Triphenylphosphin/Azodicarbonsäureester / The Unusual Reaction of 1,2-5,6-Di-O-isopropylidene Glucofuranose (Diacetoneglucose) with the System Triphenylphosphine/Azodicarboxylate Zeitschrift FüR Naturforschung B. 33: 1009-1011. DOI: 10.1515/Znb-1978-0913 |
0.307 |
|
| 1978 |
Horner L, Walach P, Kunz H. PHOSPHORORGANISCHE VERBINDUNGEN 871SYNTHESE UND REAKTIONEN CYCLISCHER PHOSPHONIUMSALZE MIT ZWEI PHOSPHORATOMEN IN SIEBEN-, ACHT-, NEUN-, ZEHN- UND ELFRINGEN SOWIE MIT VIER PHOSPHORATOMEN IN SECHZEHN-, ACHTZEHN- UND ZWANZIGRINGEN Phosphorous and Sulfur and the Related Elements. 5: 171-184. DOI: 10.1080/03086647808069882 |
0.525 |
|
| 1978 |
Weißmüller J, Kunz H. Synthese und eigenschaften von 1-desoxy-hex-1-enopyran-3-ulosen Tetrahedron Letters. 19: 3807-3808. DOI: 10.1016/S0040-4039(01)95064-6 |
0.353 |
|
| 1978 |
Kunz H. Syntheses with 2-Phosphonioethoxycarbonyl Protecting Groups: Peptide Synthesis in Water Angewandte Chemie International Edition in English. 17: 67-68. DOI: 10.1002/Anie.197800671 |
0.345 |
|
| 1976 |
HORNER L, KUNZ H, WALACH P. ChemInform Abstract: Phosphororganische Verbindungen. 81. Mitt. Synthese höhergliedriger Oligo-phosphacycloalkane. Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/Chin.197646292 |
0.537 |
|
| 1976 |
KUNZ H. ChemInform Abstract: THE 2-(TRIPHENYLPHOSPHONIO)ETHOXYCARBONYL GROUP AS AN AMINO PROTECTIVE FUNCTION IN PEPTIDE CHEMISTRY Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/Chin.197643355 |
0.342 |
|
| 1976 |
Kunz H. Der 2-(Methylthio)äthoxycarbonyl-Rest als Zweistufen-Schutzgruppe für die Aminofunktion in Aminosäuren und Peptiden Chemische Berichte. 109: 3693-3706. DOI: 10.1002/Cber.19761091123 |
0.375 |
|
| 1976 |
Kunz H. Der 2‐(Triphenylphosphonio)äthoxycarbonyl‐Rest als Schutzgruppe für die Aminofunktion in Aminosäuren und Peptiden Chemische Berichte. 109: 2670-2683. DOI: 10.1002/Cber.19761090803 |
0.362 |
|
| 1975 |
Kunz H. Notiz über die alkalische Hydrolyse des starren cyclischen Acetylcholin-Derivats N-(2-exo-Acetoxy-3-exo-norbornyl)-trimethylammoniumjodid Justus Liebigs Annalen Der Chemie. 1975: 1229-1231. DOI: 10.1002/Jlac.197519750620 |
0.325 |
|
| 1971 |
Horner L, Kunz H. Phosphororganische Verbindungen, 68. Darstellung und Eigenschaften von Tetrakis(diphenylphosphin)-nickel(0) Chemische Berichte. 104: 717-721. DOI: 10.1002/Cber.19711040308 |
0.495 |
|
| 1970 |
Horner L, Hofer W, Ertel I, Kunz H. Phosphororganische Verbindungen 65. Mitt. Selektive Abspaltung Von Allylgruppen Aus Allylphosphonium‐, ‐Arsonium‐ Und ‐Sulfoniumsalzen Und Aus Allylsulfonen Durch ′Cyanolyse′ Cheminform. 1. DOI: 10.1002/Chin.197047019 |
0.461 |
|
| 1970 |
Horner L, Hofer W, Ertel I, Kunz H. Phosphororganische Verbindungen, 65. Die selektive Abspaltung von Allylgruppen aus Allylphosphonium-, -arsonium- und -sulfoniumsalzen und aus Allylsulfonen durch „Cyanolys” Chemische Berichte. 103: 2718-2728. DOI: 10.1002/Cber.19701030903 |
0.552 |
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