| Year |
Citation |
Score |
| 2019 |
Knorr R, Schmidt B, von Roman T. α-Deprotonation of a β-shielded acrylamide creates a distorted lithium 1-aminoallen-1-olate Journal of Organometallic Chemistry. 894: 78-83. DOI: 10.1016/J.Jorganchem.2019.04.031 |
0.379 |
|
| 2018 |
Knorr R, Schmidt B. Nucleofugal behavior of a β-shielded α-cyanovinyl carbanion. Beilstein Journal of Organic Chemistry. 14: 3018-3024. PMID 30591825 DOI: 10.3762/Bjoc.14.281 |
0.364 |
|
| 2018 |
Knorr R, Schmidt B, Freudenreich J, von Roman T. β-Shielded Michael systems whose H–C(sp2) deprotonation and 1,2-addition reactions compete for organolithiums Tetrahedron. 74: 7466-7471. DOI: 10.1016/J.Tet.2018.11.020 |
0.364 |
|
| 2018 |
Knorr R, Lattke E, Ruhdorfer J, Ferchland K, von Roman U. Why is cis / trans stereoinversion with Li + (THF) 4 migration across the phenyl ring of α-lithiostyrene accelerated by two ortho -methyl groups? Tetrahedron. 74: 1621-1631. DOI: 10.1016/J.Tet.2018.01.047 |
0.369 |
|
| 2018 |
Knorr R, Schmidt B, Mehlstäubl J, von Roman T. Structures and stereoinversions of β-shielded α-Li (or K or Cs)-acrylonitriles: A mechanism with neighborly assistance Journal of Organometallic Chemistry. 871: 185-196. DOI: 10.1016/J.Jorganchem.2018.07.012 |
0.334 |
|
| 2018 |
Knorr R, Neuner B. Regioselective Dialkylations of N
-(tert
-Butyl)iminocyclopentane via
Deprotonating One-Pot Procedures Helvetica Chimica Acta. 101: e1800037. DOI: 10.1002/Hlca.201800037 |
0.377 |
|
| 2017 |
Knorr R, Behringer C, Knittl M, von Roman U, Lattke E. Doubly Diastereoconvergent Preparation and Microsolvation-Controlled Properties of (Z)- and (E)-1´-Lithio-1´-(2,6-dimethylphenyl)propenes. Journal of the American Chemical Society. PMID 28257577 DOI: 10.1021/Jacs.6B11003 |
0.325 |
|
| 2017 |
Knorr R, Knittl M, Behringer C, Ruhdorfer J, Böhrer P. Kinetics of alpha-(2,6-Dimethylphenl)vinyllithium: How to control Errors caused by inefficient Mixing with Pairs of rapidly competing Ketones. The Journal of Organic Chemistry. PMID 28186756 DOI: 10.1021/Acs.Joc.6B02686 |
0.318 |
|
| 2016 |
Knorr R, Stephenson DS, Lattke E, Böhrer P, Ruhdorfer J. Unusual traits of cis and trans-2,3-dibromo-1,1-dimethylindane on the way from 1,1-dimethylindene to 2-bromo-, 3-bromo-, and 2,3-dibromo-1,1-dimethylindene. Beilstein Journal of Organic Chemistry. 12: 1178-84. PMID 27559369 DOI: 10.3762/Bjoc.12.113 |
0.332 |
|
| 2016 |
Knorr R, Lattke E, Ruhdorfer J, von Roman U, Firl J, Böhrer P. What can 13C and 1H NMR lithiation shifts tell us about the charge distribution in α-arylvinyllithium compounds? Journal of Organometallic Chemistry. 824: 61-72. DOI: 10.1016/J.Jorganchem.2016.09.029 |
0.306 |
|
| 2015 |
Knorr R, Behringer C, Lattke E, von Roman U, Knittl M. How Microsolvation Numbers at Li Control Aggregation Modes, sp(2)-Stereoinversion, and NMR Coupling Constants (2)JH,H of H2C═C in α-(2,6-Dimethylphenyl)vinyllithium. The Journal of Organic Chemistry. 80: 6313-22. PMID 26029794 DOI: 10.1021/Acs.Joc.5B00762 |
0.375 |
|
| 2015 |
Knorr R, Ruhdorfer J, Böhrer P. Microsolvation, Dimerization, and sp2-Stereoinversion of Monomeric α-(2,6-Diisopropylphenyl)vinyllithium Organometallics. 34: 1038-1045. DOI: 10.1021/Om5010995 |
0.381 |
|
| 2014 |
Knorr R, Knittl M, Rossmann EC. Microsolvation and sp(2)-stereoinversion of monomeric α-(2,6-di-tert-butylphenyl)vinyllithium as measured by NMR. Beilstein Journal of Organic Chemistry. 10: 2521-30. PMID 25383123 DOI: 10.3762/Bjoc.10.263 |
0.398 |
|
| 2014 |
Knorr R, Menke T, Freudenreich J, Pires C. Carbenoid-mediated nucleophilic "hydrolysis" of 2-(dichloromethylidene)-1,1,3,3-tetramethylindane with DMSO participation, affording access to one-sidedly overcrowded ketone and bromoalkene descendants(§). Beilstein Journal of Organic Chemistry. 10: 307-15. PMID 24611079 DOI: 10.3762/Bjoc.10.28 |
0.324 |
|
| 2014 |
Knorr R, Rossmann EC, Knittl M, Böhrer P. Highly syn selective addition of aqueous HBr to hydrophobically shielded arylalkynes Tetrahedron. 70: 5332-5338. DOI: 10.1016/J.Tet.2014.05.002 |
0.361 |
|
| 2014 |
Knorr R, Menke T, Hennig K, Freudenreich J, Böhrer P, Schubert B. Ring expansion and vinylic nucleophilic substitution competing for (tert-alkyl)2CC(Li)–Cl in carbenoid chain processes Tetrahedron. 70: 2703-2710. DOI: 10.1016/J.Tet.2014.03.004 |
0.384 |
|
| 2014 |
Knorr R, Hennig K, Böhrer P, Schubert B. Microsolvation, aggregation, and pseudomonomolecular, ionic sp2-stereoinversion mechanism of two exocyclic β,β-di-tert-alkyl-α-arylvinyllithiums Journal of Organometallic Chemistry. 767: 125-135. DOI: 10.1016/J.Jorganchem.2014.05.031 |
0.356 |
|
| 2013 |
Knorr R, Menke T, Behringer C, Ferchland K, Mehlstäubl J, Lattke E. Pseudomonomolecular, Ionic sp2-Stereoinversion Mechanism of 1-Aryl-1-alkenyllithiums Organometallics. 32: 4070-4081. DOI: 10.1021/Om4000852 |
0.346 |
|
| 2012 |
Knorr R, Stephenson DS. Deuterium quantification through deuterium-induced remote 1H and 13C NMR shifts. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 7501-5. PMID 22566370 DOI: 10.1002/Chem.201102865 |
0.327 |
|
| 2011 |
Knorr R. Acylation Mechanisms of DMSO/[D6]DMSO with Di-tert-butylketene and Its Congeners European Journal of Organic Chemistry. 2011: 6335-6342. DOI: 10.1002/Ejoc.201100936 |
0.345 |
|
| 2010 |
Knorr R, Rossmann E, Knittl M. Easier Preparation of 2,6-Di-tert-butylphenyl Derivatives¹ Synthesis. 2010: 2124-2128. DOI: 10.1055/S-0029-1218797 |
0.402 |
|
| 2008 |
Knorr R, Menke T, Ferchland K, Mehlstäubl J, Stephenson DS. Microsolvation and 13C-Li NMR coupling. Journal of the American Chemical Society. 130: 14179-88. PMID 18828636 DOI: 10.1021/Ja8026828 |
0.35 |
|
| 2007 |
Knorr R, Hauer H, Weiss A, Polzer H, Ruf F, Löw P, Dvortsak P, Böhrer P. Unpaired spin densities from NMR shifts and magnetic anisotropies of pseudotetrahedral cobalt(II) and nickel(II) vinamidine bis(chelates). Inorganic Chemistry. 46: 8379-90. PMID 17764173 DOI: 10.1021/Ic700656R |
0.331 |
|
| 2007 |
Knorr R, Pires C, Freudenreich J. Carbenoid chain reactions through proton, deuteron, or bromine transfer from unactivated 1-bromo-1-alkenes to organolithium compounds. The Journal of Organic Chemistry. 72: 6084-90. PMID 17625883 DOI: 10.1021/Jo070623W |
0.329 |
|
| 2006 |
Knorr R, Pires C, Behringer C, Menke T, Freudenreich J, Rossmann EC, Böhrer P. Carbenoid chain reactions: substitutions by organolithium compounds at unactivated 1-chloro-1-alkenes. Journal of the American Chemical Society. 128: 14845-53. PMID 17105294 DOI: 10.1021/Ja0649116 |
0.328 |
|
| 2006 |
Knorr R, Donhärl A, Hennig K. Sterically Congested Molecules, 16 A Convenient Synthesis of Di-tert-butyl Ketone via its Imine, 2,2,4,4-tetramethyl-3-pentanimine Liebigs Annalen. 1996: 155-157. DOI: 10.1002/Jlac.199619960202 |
0.337 |
|
| 1999 |
Huisgen R, Li X, Mloston G, Knorr R, Huber H, Stephenson DS. Thiocarbonyl ylides and electrophilic azo compounds; sterically hindered cyclic hydrazodicarboxylic esters Tetrahedron. 55: 12783-12796. DOI: 10.1016/S0040-4020(99)00790-5 |
0.506 |
|
| 1997 |
Knorr R, Behringer C, Lattke E, Räpple E, Nöth H, Schmidt M. (EIZ)-Equilibria, 19 Dimeric α-Lithio-2,6-dimethylstyrene Chemische Berichte. 130: 585-592. DOI: 10.1002/Cber.19971300509 |
0.402 |
|
| 1995 |
Knorr R, Ferchland K. Sterically congested molecules, 14. Imine protonation in toluene solution: A problem akin to theN-protonation in rhodopsin Liebigs Annalen. 1995: 419-425. DOI: 10.1002/Jlac.199519950251 |
0.343 |
|
| 1994 |
Knorr R, Freudenreich J, Polborn K, Nöth H, Linti G. A β,β-shielded vinyllithium example for a quantification of structure, monomer-dimer equilibrium, and some reactivity parameters Tetrahedron. 50: 5845-5860. DOI: 10.1016/S0040-4020(01)90440-5 |
0.37 |
|
| 1994 |
Knorr R, Ferchland K, Hoang TP. Sterically Congested Molecules, 12. Acidity Constants of Sterically Shielded Protonated Imines in Hydroxylic Solvents Liebigs Annalen Der Chemie. 1994: 943-948. DOI: 10.1002/Jlac.199419940916 |
0.344 |
|
| 1994 |
Knorr R, Ruhdorfer J, Böhrer P, Bronberger H, Räpple E. Sterically Congested Molecules, 11. The 2,6-Diisopropylphenyl Substituent at CC and CN Groups Liebigs Annalen Der Chemie. 1994: 433-438. DOI: 10.1002/Jlac.199419940417 |
0.391 |
|
| 1993 |
Von Roman U, Ruhdorfer J, Knorr R. Alkenyl Bromides by Brominative Deoxygenation of Ketones in One or Two Steps Synthesis. 1993: 985-992. DOI: 10.1055/S-1993-25986 |
0.337 |
|
| 1993 |
Knorr R, Freudenreich J, von Roman T, Mehlstäubl J, Böhrer P. 1,1,3,3-tetramethyl-2-methyleneindan derivatives: syntheses with imminent rearrangement Tetrahedron. 49: 8837-8854. DOI: 10.1016/S0040-4020(01)81904-9 |
0.351 |
|
| 1993 |
Knorr R, von Roman T, Freudenreich J, Hoang TP, Mehlstäubl J, Böhrer P, Stephenson DS, Huber H, Schubert B. Substituent-induced chemical shifts along CC double bonds Magnetic Resonance in Chemistry. 31: 557-565. DOI: 10.1002/Mrc.1260310608 |
0.387 |
|
| 1993 |
Knorr R, Stephenson DS, Böhrer P, Hoang T. Substituent-induced chemical shifts (SCS) by the phenyl group in sterically congested styrene derivatives Magnetic Resonance in Chemistry. 31: 388-393. DOI: 10.1002/Mrc.1260310415 |
0.357 |
|
| 1993 |
Knorr R, Ruhdorfer J, Mehlstäubl J, Böhrer P, Stephenson DS. (E, Z)1-Equilibria, 17 Demonstration of the Nitrogen Inversion Mechanism of Imines in a Schiff Base Model Chemische Berichte. 126: 747-754. DOI: 10.1002/Cber.19931260327 |
0.359 |
|
| 1993 |
Knorr R, Hoang TP, Mehlstäubl J, Hintermeyer-;Hilpert M, Lüdemann H, Lang E, Sextl G, Rattay W, Bührer P. Sterically Congested Molecules, 6. Lone Electron Pair Donor Quality of the Imino Function: Increased Front Strain and Electronic Substituent Effects on Sterically Accelerated Nitrogen Inversion in Iminocyclopentanes Chemische Berichte. 126: 217-224. DOI: 10.1002/Cber.19931260130 |
0.335 |
|
| 1993 |
Knorr R, Hintermeyer-;Hilpert M, Mehlstäubl J, Hoang TP, Neuner B, Bührer P. (E/Z) Equilibria, 16. Lone Electron Pair Donor Quality of the Imino Function: Synthesis and Reactivity of Sterically Strongly Congested Iminocyclopentanes Chemische Berichte. 126: 211-215. DOI: 10.1002/Cber.19931260129 |
0.337 |
|
| 1992 |
Knorr R, Phung HT, Noeth H, Linti G. Sterically congested molecules. 5. Trimeric [.alpha.-(1,1,3,3-tetramethyl-2-indanylidene)benzyl]lithium: structural example of an unsolvated vinyllithium derivative Organometallics. 11: 2669-2673. DOI: 10.1021/Om00043A060 |
0.335 |
|
| 1992 |
Knorr R, Ferchland K, Mehlstäubl J, Hoang TP, Böhrer P, Lüdemann H, Lang E. (E,Z)-Gleichgewichte, 15. Synthesen und erhöhte Konfigurationslabilität von 2-Iminoindan-Derivaten mit Vorderseitenspannung Chemische Berichte. 125: 2041-2049. DOI: 10.1002/Cber.19921250912 |
0.335 |
|
| 1992 |
Knorr R, Ferchland K, Mehlstäubl J, Böhrer P, Hoang TP, Stephenson DS. (E,Z) Equilibria, 14. Substituent-Induced Chemical Shifts along the C = N Bond of Schiff Bases Chemische Berichte. 125: 2033-2040. DOI: 10.1002/Cber.19921250911 |
0.384 |
|
| 1991 |
Knorr R, Dietrich H, Mahdi W. Molecular Structures of a Lithiated Schiff Base and a Related Dialkyl Ketone Imine Chemische Berichte. 124: 2057-2063. DOI: 10.1002/Cber.19911240930 |
0.312 |
|
| 1990 |
Böhrer G, Böhrer P, Knorr R. Cyclopropan-Derivate, 3. (1-Alkylcyclopropyl)ketone durch Acylierung von α-substituierten γ-Lactonen Chemische Berichte. 123: 2167-2172. DOI: 10.1002/Cber.19901231113 |
0.4 |
|
| 1990 |
Böhrer G, Knorr R, Böhrer P. Cyclopropan-Derivate, 2. Selbst-Acylierung der α-Alkyl-γ-lactone zu Herstellung von Bis(1-alkylcyclopropyl)ketonen über Spiro[4.4]acetale Chemische Berichte. 123: 2161-2166. DOI: 10.1002/Cber.19901231112 |
0.41 |
|
| 1990 |
Knorr R, Hintermeyer-Hilpert M, Böhrer P. (E,Z) Equilibria, 12. Differential NMR Shielding by Phenyl, Assigned from Chemical Labelling and (Z,E) Equilibration Chemische Berichte. 123: 1137-1141. DOI: 10.1002/Cber.19901230529 |
0.385 |
|
| 1989 |
Knorr R, Mehlstäubl J, Böhrer P. Erschöpfende α‐Alkylierung von Fünfring‐Ketonen mit Natriumhydrid und Dimethylsulfat oder Ethyliodid Chemische Berichte. 122: 1791-1793. DOI: 10.1002/Cber.19891220927 |
0.413 |
|
| 1986 |
KNORR R, RUF F, HOEGERL J, HILPERT M, HASSEL P. ChemInform Abstract: Paramagnetically Induced NMR Shifts. Part 12. (1-Alkoxyalkyl)malonaldehyde Dianils by Aldimine Reduction of Formylmalonaldehyde Dianil and 1,3-Migration of the Anilino Group. Chemischer Informationsdienst. 17. DOI: 10.1002/Chin.198611174 |
0.307 |
|
| 1985 |
Ruf F, Högerl J, Knorr R, Bronberger H. (1‐Alkenyl)malonaldehyd‐dianile aus Formylmalonaldehyd‐dianil Chemische Berichte. 118: 4754-4759. DOI: 10.1002/Cber.19851181210 |
0.391 |
|
| 1985 |
Knorr R, Ruf F, Högerl J, Hilpert M, Hassel P. (1-Alkoxyalkyl)malonaldehyd-dianile. aus Formylmalonaldehyd-dianil durch Aldimin-Reduktion und 1,3-Anilin-Verschiebung Chemische Berichte. 118: 4743-4753. DOI: 10.1002/Cber.19851181209 |
0.348 |
|
| 1984 |
Böhrer G, Knorr R. Tetrakis (1-methylcyclopropyl) ethylene in four steps from α-methyl-γ-butyrolactone Tetrahedron Letters. 25: 3675-3678. DOI: 10.1016/0040-4039(84)80102-1 |
0.378 |
|
| 1984 |
KNORR R, VON ROMAN T. ChemInform Abstract: E/Z EQUILIBRIA. PART 9. CONFIGURATION STABILITY OF VINYLLITHIUM DERIVATIVES WITH 1-TRIMETHYLSILYL AND 1-ALKOXY SUBSTITUENTS Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198436060 |
0.327 |
|
| 1984 |
Knorr R, Loew P, Hassel P, Bronberger H. Malonaldehyde derivatives: a general one- or two-step synthesis from substituted acetic acids The Journal of Organic Chemistry. 49: 1288-1290. DOI: 10.1002/Chin.198435163 |
0.317 |
|
| 1984 |
KNORR R, LOEW P, HASSEL P. ChemInform Abstract: ALDEHYDE-DERIVED ENAMINES; A NEW ONE-POT SYNTHESIS FROM SUBSTITUTED ACETIC ACIDS Chemischer Informationsdienst. 15. DOI: 10.1002/Chin.198405152 |
0.316 |
|
| 1984 |
Knorr R, von Roman TF. Configurational Stability of Vinyllithium Derivatives with 1-Trimethylsilyl and 1-Alkoxy Substituents Angewandte Chemie International Edition in English. 23: 366-368. DOI: 10.1002/Anie.198403661 |
0.302 |
|
| 1984 |
Knorr R, von Roman TF. Zur Konfigurationsstabilität von Vinyllithiumderivaten mit 1-Trimethylsilyl- und 1-Alkoxy-Substituenten Angewandte Chemie. 96: 349-350. DOI: 10.1002/Ange.19840960507 |
0.322 |
|
| 1982 |
Knorr R, Weiß A. Synthesen und Eigenschaften hochsubstituierter Vinamidine Chemische Berichte. 115: 139-160. DOI: 10.1002/Cber.19821150115 |
0.417 |
|
| 1981 |
Knorr R. Inductive substituent constants σji from olefinic geminal 1h, 1h nmr coupling constants Tetrahedron. 37: 929-938. DOI: 10.1016/S0040-4020(01)97662-8 |
0.367 |
|
| 1981 |
KNORR R, LATTKE E, RAEPPLE E. ChemInform Abstract: E/Z EQUILIBRIUM. VII. CONFORMATIONAL ORTHO EFFECT IN O-TOLYLSTILBENES AND THEIR VINYLLITHIUM DERIVATIVES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198134092 |
0.317 |
|
| 1981 |
KNORR R, LATTKE E, RUF F, REISSIG H. ChemInform Abstract: VINYL-TO-BENZYL ISOMERIZATION AND ELECTROCYCLIZATIONS IN LITHIO DERIVATIVES OF O-TOLYLSTILBENES Chemischer Informationsdienst. 12. DOI: 10.1002/Chin.198133163 |
0.455 |
|
| 1981 |
Knorr R, Lattke E. 2-Methyl-1-phenyl-1-propenyllithium. Ein katalytisch ummetallierbares Vinyllithiumderivat Chemische Berichte. 114: 2116-2131. DOI: 10.1002/Cber.19811140612 |
0.401 |
|
| 1981 |
Knorr R, Weiß A. Konfigurationsstabilität und reduzierte 1H-NMR-Verschiebungen (pseudo)tetraedrischer Nickel(II)-Bis-chelate von 1,3-Diiminen1) Chemische Berichte. 114: 2104-2115. DOI: 10.1002/Cber.19811140611 |
0.33 |
|
| 1981 |
Lattke E, Knorr R. 1-Phenyl-2,2-di(o-tolyl)vinyllithiumE/Z-Topomerisierung, Vinyl-Benzyl-Isomerisierung und Elektrocyclisierungen1,2) Chemische Berichte. 114: 1600-1609. DOI: 10.1002/Cber.19811140504 |
0.407 |
|
| 1981 |
Knorr R, Lattke E, Ruf F, Reißig H. Vinyl-to-Benzyl Isomerization and Electrocyclizations in Lithio Derivatives ofo-Tolylstilbenes Chemische Berichte. 114: 1592-1599. DOI: 10.1002/Cber.19811140503 |
0.542 |
|
| 1981 |
Knorr R, Lattke E, Räpple E. Der konformative ortho‐Effekt bei o‐Tolylstilbenen und deren Vinyllithiumderivaten1,2) Chemische Berichte. 114: 1581-1591. DOI: 10.1002/Cber.19811140502 |
0.411 |
|
| 1980 |
Knorr R, Lattke E, Räpple E. Zur Bildung und Reaktivität di‐tert‐alkylsubstituierter Phenylalkene European Journal of Organic Chemistry. 1980: 1207-1215. DOI: 10.1002/Jlac.198019800805 |
0.32 |
|
| 1980 |
KNORR R, LATTKE E, RAEPPLE E. ChemInform Abstract: FORMATION AND REACTIVITY OF DI-TERT-ALKYL-SUBSTITUTED PHENYLALKENES Chemischer Informationsdienst. 11. DOI: 10.1002/Chin.198048168 |
0.377 |
|
| 1980 |
Knorr R, Weiß A, Löw P, Räpple E. Azomethine, 1‐Azaallyl‐Anionen und metastabile sek. Enamine Chemische Berichte. 113: 2462-2489. DOI: 10.1002/Cber.19801130714 |
0.385 |
|
| 1980 |
Knorr R. Empirical Substituent Parameters forE/Z Equilibrium Constants Chemische Berichte. 113: 2441-2461. DOI: 10.1002/Cber.19801130713 |
0.344 |
|
| 1979 |
Knorr R, Schnegg A, Lattke E, Räpple E. 1H-Kernresonanzverschiebungen in der Gerüstebene anisotroper CO-, CN- und CC-Doppelbindungen Chemische Berichte. 112: 3490-3514. DOI: 10.1002/Cber.19791121017 |
0.319 |
|
| 1977 |
Knorr R, Weiss A. Configurationally rigid tetrahedral nickel complexes used for conformational analysis of cycloalkene units Journal of the Chemical Society, Chemical Communications. 173-174. DOI: 10.1039/C39770000173 |
0.317 |
|
| 1977 |
Knorr R, Lattke E. Configurational Isomerization of α-aryl-vinyllithium: kinetics, mechanism, and steric acceleration Tetrahedron Letters. 18: 3969-3972. DOI: 10.1016/S0040-4039(01)83405-5 |
0.315 |
|
| 1972 |
GLAZER ES, KNORR R, GANTER C, ROBERTS JD. ChemInform Abstract: NMR-SPEKTROSKOPIE, KONFORMATIONSGLEICHGEWICHTE VON CYCLOHEPTAN- UND CYCLOHEPTENDERIVATEN Chemischer Informationsdienst. 3: no-no. DOI: 10.1002/Chin.197245129 |
0.346 |
|
| 1971 |
Knorr R. Zum Mechanismus der Dakin-West-Reaktion, III. Der Verlauf der Ringöffnung bei der Dakin-West-Reaktion eines Oxazolium-5-olats Chemische Berichte. 104: 3633-3643. DOI: 10.1002/Cber.19711041129 |
0.345 |
|
| 1971 |
Knorr R, Staudinger GK. Zum Mechanismus der Dakin-West-Reaktion, II. Kinetik und Mechanismus der Dakin-West-Reaktion bei N-Acyl-sek.-aminosäuren Chemische Berichte. 104: 3621-3632. DOI: 10.1002/Cber.19711041128 |
0.333 |
|
| 1970 |
Knorr R, Huisgen R. [The reaction of N-acyl-sec-amino acids with acetic anhydride]. Chemische Berichte. 103: 2598-610. PMID 5448834 DOI: 10.1002/Cber.19701030831 |
0.487 |
|
| 1970 |
BAYER HO, HUISGEN R, KNORR R, SCHAEFER FC. ChemInform Abstract: DARST. UND EIGENSCHAFTEN MESOIONISCHER OXAZOLONE Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197044325 |
0.463 |
|
| 1970 |
KNORR R, HUISGEN R. ChemInform Abstract: MECHANISMUS DER DAKIN-WEST-RK. 1. MITT. RK. VON N-ACYL-SEK.-AMINOSAEUREN MIT ACETANHYDRID Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197044204 |
0.457 |
|
| 1970 |
KNORR R, HUISGEN R, STAUDINGER GK. ChemInform Abstract: 1,3-DIPOLARE CYCLOADDITIONEN 58. MITT. KINETIK DER CYCLOADDITIONEN EINES OXAZOLIUM-5-OXIDS Chemischer Informationsdienst. Organische Chemie. 1: no-no. DOI: 10.1002/Chin.197044154 |
0.418 |
|
| 1970 |
Knorr R, Huisgen R, Staudinger GK. 1.3-Dipolare Cycloadditionen, LVIII. Kinetik der Cycloadditionen eines Oxazolium-5-oxids Chemische Berichte. 103: 2639-2646. DOI: 10.1002/Cber.19701030834 |
0.472 |
|
| 1970 |
Bayer HO, Huisgen R, Knorr R, Schaefer FC. Darstellung und Eigenschaften mesoionischer Oxazolone Chemische Berichte. 103: 2581-2597. DOI: 10.1002/Cber.19701030830 |
0.502 |
|
| 1969 |
Seidl H, Huisgen R, Knorr R. 1.3-Dipolare Cycloadditionen, XLVI. Zur Anlagerung der Nitrone an CC-Dreifachbindungen Chemische Berichte. 102: 904-914. DOI: 10.1002/Cber.19691020324 |
0.449 |
|
| 1968 |
Gotthardt H, Huisgen R, Knorr R. 1.3-Dipolare Cycloadditionen, XXXVIII. Reaktionen der Sydnone mit Benz-in und mit einigen Heteromehrfachbindungen Chemische Berichte. 101: 1056-1058. DOI: 10.1002/Cber.19681010342 |
0.477 |
|
| 1967 |
Huisgen R, Funke E, Schaefer FC, Knorr R. Possible Valence Tautomerism of a Mesoionic Oxazol-5-one with an Acylaminoketene Angewandte Chemie International Edition in English. 6: 367-368. DOI: 10.1002/Anie.196703671 |
0.416 |
|
| 1967 |
Huisgen R, Funke E, Knorr R, Schaefer FC. Valenztautomerie eines mesoionischen Oxazol-5-ons mit einem Acylamino-keten? Angewandte Chemie. 79: 321-321. DOI: 10.1002/Ange.19670790721 |
0.49 |
|
| 1965 |
Huisgen R, Knorr R, Möbius L, Szeimies G. 1.3‐Dipolare Cycloadditionen, XXIII. Einige Beobachtungen zur Addition organischer Azide an CC‐Dreifachbindungen Chemische Berichte. 98: 4014-4021. DOI: 10.1002/Cber.19650981228 |
0.629 |
|
| 1961 |
Huisgen R, Knorr R. Benz-in als Dipolarophil Die Naturwissenschaften. 48: 716-716. DOI: 10.1007/Bf00620961 |
0.406 |
|
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