Herbert Mayr, Ph.D. - Publications

Affiliations: 
1984 University of Munich, München, Bayern, Germany 
Website:
http://www.cup.uni-muenchen.de/oc/mayr/CDmayrcv.html

127 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Mayer RJ, Breugst M, Hampel N, Ofial AR, Mayr H. Ambident Reactivity of Phenolate Anions Revisited: A Quantitative Approach to Phenolate Reactivities. The Journal of Organic Chemistry. PMID 31241938 DOI: 10.1021/acs.joc.9b01485  0.72
2018 Jangra H, Chen Q, Fuks E, Zenz I, Mayer P, Ofial AR, Zipse H, Mayr H. Nucleophilicity and Electrophilicity Parameters for Predicting Absolute Rate Constants of Highly Asynchronous 1,3-Dipolar Cycloadditions of Aryldiazomethanes. Journal of the American Chemical Society. PMID 30444361 DOI: 10.1021/jacs.8b09995  0.72
2018 Timofeeva DS, Ofial AR, Mayr H. Kinetics of Electrophilic Fluorinations of Enamines and Carbanions: Comparison of the Fluorinating Power of N-F Reagents. Journal of the American Chemical Society. PMID 30156412 DOI: 10.1021/jacs.8b07147  0.72
2018 Li Z, Jangra H, Chen Q, Mayer P, Ofial AR, Zipse H, Mayr H. Kinetics and Mechanism of Oxirane Formation by Darzens Condensation of Ketones: Quantification of the Electrophilicities of Ketones. Journal of the American Chemical Society. PMID 29659264 DOI: 10.1021/jacs.8b01657  0.72
2018 Timofeeva DS, Mayer R, Mayer P, Ofial A, Mayr H. Which Factors Control the Nucleophilic Reactivities of Enamines? Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29388720 DOI: 10.1002/chem.201705962  0.36
2017 Allgäuer DS, Jangra H, Asahara H, Li Z, Chen Q, Zipse H, Ofial AR, Mayr H. Quantification and Theoretical Analysis of the Electrophilicities of Michael Acceptors. Journal of the American Chemical Society. PMID 28921959 DOI: 10.1021/jacs.7b05106  0.72
2017 Mayer R, Tokuyasu T, Mayer P, Gomar J, Sabelle S, Mennucci B, Mayr H, Ofial AR. Solvation Accounts for the Counter-Intuitive Nucleophilicity Ordering of Peroxide Anions. Angewandte Chemie (International Ed. in English). PMID 28815833 DOI: 10.1002/anie.201707086  0.72
2017 Li Z, Chen Q, Mayer P, Mayr H. Nucleophilicity parameters of arylsulfonyl substituted halomethyl anions. The Journal of Organic Chemistry. PMID 28106995 DOI: 10.1021/acs.joc.6b02844  0.36
2017 Byrne PA, Kobayashi S, Würthwein EU, Ammer J, Mayr H. Why are Vinyl Cations Sluggish Electrophiles? Journal of the American Chemical Society. PMID 28040896 DOI: 10.1021/jacs.6b10889  0.56
2016 Chelli S, Troshin K, Mayer P, Lakhdar S, Ofial AR, Mayr H. Nucleophilicity Parameters of Stabilized Iodonium Ylides for Characterizing their Synthetic Potential. Journal of the American Chemical Society. PMID 27428876 DOI: 10.1021/jacs.6b05768  1
2016 Chen Q, Mayer P, Mayr H. Ethenesulfonyl Fluoride: The Most Perfect Michael Acceptor Ever Found? Angewandte Chemie (International Ed. in English). PMID 27159425 DOI: 10.1002/anie.201601875  0.36
2016 Mayr H, Ofial AR. Philicities, Fugalities, and Equilibrium Constants. Accounts of Chemical Research. PMID 27108991 DOI: 10.1021/acs.accounts.6b00071  0.72
2016 Chelli S, Troshin K, Lakhdar S, Mayr H, Mayer P. Crystal structure of 2-[chloro-(4-meth-oxy-phen-yl)meth-yl]-2-(4-meth-oxy-phen-yl)-5,5-di-methyl-cyclo-hexane-1,3-dione. Acta Crystallographica. Section E, Crystallographic Communications. 72: 300-3. PMID 27006792 DOI: 10.1107/S2056989016002085  1
2016 Chelli S, Troshin K, Lakhdar S, Mayr H, Mayer P. Crystal structure of (1S,2R)-6,6-dimethyl-4,8-dioxo-2-phenyl-spiro-[2.5]octane-1-carbaldehyde. Acta Crystallographica. Section E, Crystallographic Communications. 72: 266-8. PMID 26958403 DOI: 10.1107/S205698901600164X  1
2016 Puente Á, He S, Corral-Bautista F, Ofial AR, Mayr H. Nucleophilic Reactivities of 2-Substituted Malonates European Journal of Organic Chemistry. DOI: 10.1002/ejoc.201600107  1
2015 Mayr H, Ofial AR. A quantitative approach to polar organic reactivity. Sar and Qsar in Environmental Research. 1-28. PMID 26315811 DOI: 10.1080/1062936X.2015.1078409  1
2015 Follet E, Berionni G, Mayer P, Mayr H. Structure and Reactivity of Indolylmethylium Ions: Scope and Limitations in Synthetic Applications. The Journal of Organic Chemistry. 80: 8643-56. PMID 26218059 DOI: 10.1021/acs.joc.5b01298  1
2015 Feeney K, Berionni G, Mayr H, Aggarwal VK. Structure and reactivity of boron-ate complexes derived from primary and secondary boronic esters. Organic Letters. 17: 2614-7. PMID 25973673 DOI: 10.1021/acs.orglett.5b00918  1
2015 Corral-Bautista F, Klier L, Knochel P, Mayr H. From Carbanions to Organometallic Compounds: Quantification of Metal Ion Effects on Nucleophilic Reactivities. Angewandte Chemie (International Ed. in English). PMID 25951612 DOI: 10.1002/anie.201501385  1
2015 Moriya K, Didier D, Simon M, Hammann JM, Berionni G, Karaghiosoff K, Zipse H, Mayr H, Knochel P. Stereoselective synthesis and reactions of secondary alkyllithium reagents functionalized at the 3-position. Angewandte Chemie (International Ed. in English). 54: 2754-7. PMID 25640227 DOI: 10.1002/anie.201409165  1
2015 Berionni G, Leonov AI, Mayer P, Ofial AR, Mayr H. Fine-tuning the nucleophilic reactivities of boron ate complexes derived from aryl and heteroaryl boronic esters. Angewandte Chemie (International Ed. in English). 54: 2780-3. PMID 25604646 DOI: 10.1002/anie.201410562  1
2015 Mayr H, Ammer J, Baidya M, Maji B, Nigst TA, Ofial AR, Singer T. Scales of Lewis basicities toward C-centered Lewis acids (carbocations). Journal of the American Chemical Society. 137: 2580-99. PMID 25555037 DOI: 10.1021/ja511639b  1
2015 Corral-Bautista F, Appel R, Frickel JS, Mayr H. Quantification of ion-pairing effects on the nucleophilic reactivities of benzoyl- and phenyl-substituted carbanions in dimethylsulfoxide. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 875-84. PMID 25384456 DOI: 10.1002/chem.201404500  1
2015 Mayr H. Reactivity scales for quantifying polar organic reactivity: the benzhydrylium methodology Tetrahedron. 71: 5095-5111. DOI: 10.1016/j.tet.2015.05.055  1
2015 Mayr H. Physical Organic Chemistry-Development and Perspectives Israel Journal of Chemistry. DOI: 10.1002/ijch.201400200  1
2015 Corral-Bautista F, Mayr H. Quantification of the Nucleophilic Reactivities of Cyclic β-Keto Ester Anions European Journal of Organic Chemistry. 2015: 7594-7601. DOI: 10.1002/ejoc.201501107  1
2014 Erdmann H, An F, Mayer P, Ofial AR, Lakhdar S, Mayr H. Structures and reactivities of 2-Trityl- and 2-(Triphenylsilyl)pyrrolidine-derived enamines: evidence for negative hyperconjugation with the trityl group. Journal of the American Chemical Society. 136: 14263-9. PMID 25220171 DOI: 10.1021/ja508065e  1
2014 Guo X, Zipse H, Mayr H. Mechanisms of hydride abstractions by quinones. Journal of the American Chemical Society. 136: 13863-73. PMID 25196576 DOI: 10.1021/ja507598y  1
2014 Chen X, Tan Y, Berionni G, Ofial AR, Mayr H. Di- and triarylmethylium ions as probes for the ambident reactivities of carbanions derived from 5-benzylated Meldrum's acid. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 11069-77. PMID 25099696 DOI: 10.1002/chem.201403161  1
2014 Guo X, Mayr H. Quantification of the ambident electrophilicities of halogen-substituted quinones. Journal of the American Chemical Society. 136: 11499-512. PMID 25053179 DOI: 10.1021/ja505613b  1
2014 Frischmuth A, Fernández M, Barl NM, Achrainer F, Zipse H, Berionni G, Mayr H, Karaghiosoff K, Knochel P. New in situ trapping metalations of functionalized arenes and heteroarenes with TMPLi in the presence of ZnCl2 and other metal salts. Angewandte Chemie (International Ed. in English). 53: 7928-32. PMID 24923789 DOI: 10.1002/anie.201403688  1
2014 Laub HA, Evano G, Mayr H. Hydrocarbation of C≡C bonds: quantification of the nucleophilic reactivity of ynamides. Angewandte Chemie (International Ed. in English). 53: 4968-71. PMID 24715471 DOI: 10.1002/anie.201402055  1
2014 Laub HA, Mayr H. Electrophilic alkylations of vinylsilanes: a comparison of α- and β-silyl effects. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 1103-10. PMID 24357501 DOI: 10.1002/chem.201303215  1
2014 Allgäuer DS, Mayr H. Electrophilicities of 1,2-disubstituted ethylenes European Journal of Organic Chemistry. 2014: 2956-2963. DOI: 10.1002/ejoc.201301779  1
2014 An F, Paul S, Ammer J, Ofial AR, Mayer P, Lakhdar S, Mayr H. Structures and reactivities of iminium ions derived from substituted cinnamaldehydes and various chiral imidazolidin-4-ones Asian Journal of Organic Chemistry. 3: 550-555. DOI: 10.1002/ajoc.201402009  1
2014 Wilcken R, Mayr H, Riedle E. Bimolecular reactions on a timescale below 1 ps Optics Infobase Conference Papers 1
2013 Maji B, Troshin K, Mayr H. Ambident reactivities of formaldehyde N,N-dialkylhydrazones. Angewandte Chemie (International Ed. in English). 52: 11900-4. PMID 24105976 DOI: 10.1002/anie.201305092  1
2013 Allgäuer DS, Mayer P, Mayr H. Nucleophilicity parameters of pyridinium ylides and their use in mechanistic analyses. Journal of the American Chemical Society. 135: 15216-24. PMID 24020381 DOI: 10.1021/ja407885h  1
2013 Ammer J, Nolte C, Karaghiosoff K, Thallmair S, Mayer P, de Vivie-Riedle R, Mayr H. Ion-pairing of phosphonium salts in solution: C-H⋅⋅⋅halogen and C-H⋅⋅⋅π hydrogen bonds. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 14612-30. PMID 24014323 DOI: 10.1002/chem.201204561  1
2013 Guo X, Mayr H. Manifestation of polar reaction pathways of 2,3-dichloro-5,6-dicyano-p-benzoquinone. Journal of the American Chemical Society. 135: 12377-87. PMID 23937562 DOI: 10.1021/ja405890d  1
2013 Maji B, Mayr H. Structures and ambident reactivities of azolium enolates. Angewandte Chemie (International Ed. in English). 52: 11163-7. PMID 23897657 DOI: 10.1002/anie.201303524  1
2013 Holland MC, Paul S, Schweizer WB, Bergander K, Mück-Lichtenfeld C, Lakhdar S, Mayr H, Gilmour R. Noncovalent interactions in organocatalysis: modulating conformational diversity and reactivity in the MacMillan catalyst. Angewandte Chemie (International Ed. in English). 52: 7967-71. PMID 23794233 DOI: 10.1002/anie.201301864  1
2013 Appel R, Chelli S, Tokuyasu T, Troshin K, Mayr H. Electrophilicities of benzaldehyde-derived iminium ions: quantification of the electrophilic activation of aldehydes by iminium formation. Journal of the American Chemical Society. 135: 6579-87. PMID 23570344 DOI: 10.1021/ja401106x  1
2013 Sailer CF, Thallmair S, Fingerhut BP, Nolte C, Ammer J, Mayr H, Pugliesi I, de Vivie-Riedle R, Riedle E. A comprehensive microscopic picture of the benzhydryl radical and cation photogeneration and interconversion through electron transfer. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. 14: 1423-37. PMID 23554328 DOI: 10.1002/cphc.201201057  1
2013 Berionni G, Morozova V, Heininger M, Mayer P, Knochel P, Mayr H. Electrophilic aromatic substitutions of aryltrifluoroborates with retention of the BF3- group: quantification of the activating and directing effects of the trifluoroborate group. Journal of the American Chemical Society. 135: 6317-24. PMID 23534556 DOI: 10.1021/ja4017655  1
2013 Troshin K, Mayr H. Electrofugalities of 1,3-diarylallyl cations. The Journal of Organic Chemistry. 78: 2649-60. PMID 23368714 DOI: 10.1021/jo302766k  1
2013 Horn M, Schappele LH, Lang-Wittkowski G, Mayr H, Ofial AR. Towards a comprehensive hydride donor ability scale. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 249-63. PMID 23203839 DOI: 10.1002/chem.201202839  1
2013 Troshin K, Mayr H. Ion pair dynamics: solvolyses of chiral 1,3-diarylallyl carboxylates as a case study. Journal of the American Chemical Society. 135: 252-65. PMID 23186244 DOI: 10.1021/ja308670g  1
2013 Maji B, Mayr H. Nucleophilic reactivities of Schiff bases Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences. 68: 693-699. DOI: 10.5560/ZNB.2013-3085  1
2013 Ammer J, Mayr H. Photogeneration of carbocations: Applications in physical organic chemistry and the design of suitable precursors Journal of Physical Organic Chemistry. 26: 956-969. DOI: 10.1002/poc.3132  1
2013 Ammer J, Mayr H. Solvent nucleophilicities of hexafluoroisopropanol/water mixtures Journal of Physical Organic Chemistry. 26: 59-63. DOI: 10.1002/poc.3064  1
2013 Allgäuer DS, Mayr H. One-pot two-step synthesis of 1-(ethoxycarbonyl)indolizines via pyridinium ylides European Journal of Organic Chemistry. 6379-6388. DOI: 10.1002/ejoc.201300784  1
2013 Corral-Bautista F, Mayr H. Quantification of the nucleophilic reactivities of ethyl arylacetate anions European Journal of Organic Chemistry. 4255-4261. DOI: 10.1002/ejoc.201300265  1
2013 Maji B, Baidya M, Ammer J, Kobayashi S, Mayer P, Ofial AR, Mayr H. Nucleophilic reactivities and Lewis basicities of 2-imidazolines and related N-heterocyclic compounds European Journal of Organic Chemistry. 3369-3377. DOI: 10.1002/ejoc.201300213  1
2012 Maji B, Berionni G, Mayr H, Mayer P. 5-[(E)-Meth-oxy(phen-yl)methyl-idene]-1,3,4-triphenyl-4,5-dihydro-1H-1,2,4-triazole. Acta Crystallographica. Section E, Structure Reports Online. 68: o3307. PMID 23468812 DOI: 10.1107/S1600536812045692  1
2012 Mayr H, Lakhdar S, Maji B, Ofial AR. A quantitative approach to nucleophilic organocatalysis. Beilstein Journal of Organic Chemistry. 8: 1458-78. PMID 23019481 DOI: 10.3762/bjoc.8.166  1
2012 Maji B, Mayr H, Mayer P. (Z)-2-[Meth-oxy(phen-yl)methyl-idene]-3,4,5-trimethyl-2,3-dihydro-1,3-thia-zole. Acta Crystallographica. Section E, Structure Reports Online. 68: o2644. PMID 22969543 DOI: 10.1107/S1600536812034137  1
2012 Maji B, Mayr H. Structures and reactivities of O-methylated Breslow intermediates. Angewandte Chemie (International Ed. in English). 51: 10408-12. PMID 22968992 DOI: 10.1002/anie.201204524  1
2012 Nigst TA, Antipova A, Mayr H. Nucleophilic reactivities of hydrazines and amines: the futile search for the α-effect in hydrazine reactivities. The Journal of Organic Chemistry. 77: 8142-55. PMID 22950800 DOI: 10.1021/jo301497g  1
2012 Troshin K, Mayer P, Mayr H. (R,E)-3-(4-Chloro-phen-yl)-1-phenyl-allyl 4-nitro-benzoate. Acta Crystallographica. Section E, Structure Reports Online. 68: o2549. PMID 22904981 DOI: 10.1107/S1600536812032813  1
2012 Nigst TA, Ammer J, Mayr H. Photogeneration of benzhydryl cations by near-UV laser flash photolysis of pyridinium salts. The Journal of Physical Chemistry. A. 116: 8494-9. PMID 22849534 DOI: 10.1021/jp3049247  1
2012 Ammer J, Nolte C, Mayr H. Free energy relationships for reactions of substituted benzhydrylium ions: from enthalpy over entropy to diffusion control. Journal of the American Chemical Society. 134: 13902-11. PMID 22839678 DOI: 10.1021/ja306522b  1
2012 Laub HA, Gladow D, Reissig HU, Mayr H. The influence of perfluorinated substituents on the nucleophilic reactivities of silyl enol ethers Organic Letters. 14: 3990-3993. PMID 22830316 DOI: 10.1021/ol301766w  1
2012 Ammer J, Sailer CF, Riedle E, Mayr H. Photolytic generation of benzhydryl cations and radicals from quaternary phosphonium salts: how highly reactive carbocations survive their first nanoseconds. Journal of the American Chemical Society. 134: 11481-94. PMID 22591218 DOI: 10.1021/ja3017522  1
2012 Berionni G, Mayer P, Mayr H. Potassium [1-(tert-but-oxy-carbon-yl)-1H-indol-3-yl]trifluoro-borate hemihydrate. Acta Crystallographica. Section E, Structure Reports Online. 68: m551-2. PMID 22590073 DOI: 10.1107/S1600536812014225  1
2012 Maji B, Horn M, Mayr H. Nucleophilic reactivities of deoxy Breslow intermediates: how does aromaticity affect the catalytic activities of N-heterocyclic carbenes? Angewandte Chemie (International Ed. in English). 51: 6231-5. PMID 22573542 DOI: 10.1002/anie.201202327  1
2012 Shi L, Chu Y, Knochel P, Mayr H. Leaving group dependence of the rates of halogen-magnesium exchange reactions. Organic Letters. 14: 2602-5. PMID 22571332 DOI: 10.1021/ol300906a  1
2012 Lakhdar S, Maji B, Mayr H. Imidazolidinone-derived enamines: nucleophiles with low reactivity. Angewandte Chemie (International Ed. in English). 51: 5739-42. PMID 22535655 DOI: 10.1002/anie.201201240  1
2012 Samanta RC, Maji B, De Sarkar S, Bergander K, Fröhlich R, Mück-Lichtenfeld C, Mayr H, Studer A. Nucleophilic addition of enols and enamines to α,β-unsaturated acyl azoliums: mechanistic studies. Angewandte Chemie (International Ed. in English). 51: 5234-8. PMID 22505234 DOI: 10.1002/anie.201109042  1
2012 Maji B, Lakhdar S, Mayr H. Nucleophilicity parameters of enamides and their implications for organocatalytic transformations. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 5732-40. PMID 22461320 DOI: 10.1002/chem.201103519  1
2012 Asahara H, Mayr H. Electrophilicities of bissulfonyl ethylenes. Chemistry, An Asian Journal. 7: 1401-7. PMID 22454302 DOI: 10.1002/asia.201101046  1
2012 Lakhdar S, Baidya M, Mayr H. Kinetics and mechanism of organocatalytic aza-Michael additions: direct observation of enamine intermediates. Chemical Communications (Cambridge, England). 48: 4504-6. PMID 22453687 DOI: 10.1039/c2cc31224g  1
2012 Asahara H, Mayer P, Mayr H. 2-(4-Meth-oxy-benzyl-idene)-2H-1,3-benzodithiole 1,1,3,3-tetra-oxide. Acta Crystallographica. Section E, Structure Reports Online. 68: o567. PMID 22412485 DOI: 10.1107/S1600536812002826  1
2012 Asahara H, Mayer P, Mayr H. 1-[2,2-Bis(phenyl-sulfon-yl)ethen-yl]-4-meth-oxy-benzene. Acta Crystallographica. Section E, Structure Reports Online. 68: o470. PMID 22347078 DOI: 10.1107/S1600536812001961  1
2012 Nolte C, Ammer J, Mayr H. Nucleofugality and nucleophilicity of fluoride in protic solvents. The Journal of Organic Chemistry. 77: 3325-35. PMID 22339036 DOI: 10.1021/jo300141z  1
2012 Joannesse C, Johnston CP, Morrill LC, Woods PA, Kieffer M, Nigst TA, Mayr H, Lebl T, Philp D, Bragg RA, Smith AD. Isothiourea-mediated asymmetric O- to C-carboxyl transfer of oxazolyl carbonates: structure-selectivity profiles and mechanistic studies. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 2398-408. PMID 22262624 DOI: 10.1002/chem.201102847  1
2012 Nigst TA, Ammer J, Mayr H. Ambident reactivities of methylhydrazines. Angewandte Chemie (International Ed. in English). 51: 1353-6. PMID 22223457 DOI: 10.1002/anie.201107315  1
2012 Breugst M, Corral Bautista F, Mayr H. Nucleophilic reactivities of the anions of nucleobases and their subunits. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 127-37. PMID 22161734 DOI: 10.1002/chem.201102411  1
2012 Horn M, Mayr H, Lacôte E, Merling E, Deaner J, Wells S, McFadden T, Curran DP. N-Heterocyclic carbene boranes are good hydride donors. Organic Letters. 14: 82-5. PMID 22149270 DOI: 10.1021/ol202836p  1
2012 Berionni G, Maji B, Knochel P, Mayr H. Nucleophilicity parameters for designing transition metal-free C-C bond forming reactions of organoboron compounds Chemical Science. 3: 878-882. DOI: 10.1039/c2sc00883a  1
2012 Troshin K, Mayer P, Mayr H. How does palladium coordination affect the electrophilicities of allyl cations? Development of a robust kinetic method for following reactions of [(η 3-diarylallyl)Pd(PPh 3) 2] + with nucleophiles Organometallics. 31: 2416-2424. DOI: 10.1021/om3000357  1
2012 Horn M, Mayr H. A comprehensive view on stabilities and reactivities of triarylmethyl cations (tritylium ions) Journal of Physical Organic Chemistry. 25: 979-988. DOI: 10.1002/poc.2979  1
2012 Maji B, Stephenson DS, Mayr H. Guanidines: Highly Nucleophilic Organocatalysts Chemcatchem. 4: 993-999. DOI: 10.1002/cctc.201200143  1
2011 Zenz I, Mayr H. Electrophilicities of trans-β-nitrostyrenes. The Journal of Organic Chemistry. 76: 9370-8. PMID 21978126 DOI: 10.1021/jo201678u  1
2011 Duan XH, Maji B, Mayr H. Characterization of the nucleophilic reactivities of thiocarboxylate, dithiocarbonate and dithiocarbamate anions. Organic & Biomolecular Chemistry. 9: 8046-50. PMID 21975968 DOI: 10.1039/c1ob06245j  1
2011 Troshin K, Schindele C, Mayr H. Electrophilicities of symmetrically substituted 1,3-diarylallyl cations. The Journal of Organic Chemistry. 76: 9391-408. PMID 21939207 DOI: 10.1021/jo201668w  1
2011 Lakhdar S, Ammer J, Mayr H. Generation of α,β-unsaturated iminium ions by laser flash photolysis. Angewandte Chemie (International Ed. in English). 50: 9953-6. PMID 21898728 DOI: 10.1002/anie.201103683  1
2011 Mayr H, Breugst M, Ofial AR. Farewell to the HSAB treatment of ambident reactivity. Angewandte Chemie (International Ed. in English). 50: 6470-505. PMID 21726020 DOI: 10.1002/anie.201007100  1
2011 Maji B, Breugst M, Mayr H. N-heterocyclic carbenes: organocatalysts with moderate nucleophilicity but extraordinarily high Lewis basicity. Angewandte Chemie (International Ed. in English). 50: 6915-9. PMID 21714052 DOI: 10.1002/anie.201102435  1
2011 Maji B, Joannesse C, Nigst TA, Smith AD, Mayr H. Nucleophilicities and Lewis basicities of isothiourea derivatives. The Journal of Organic Chemistry. 76: 5104-12. PMID 21568333 DOI: 10.1021/jo200803x  1
2011 Appel R, Mayr H. Quantification of the electrophilic reactivities of aldehydes, imines, and enones. Journal of the American Chemical Society. 133: 8240-51. PMID 21553901 DOI: 10.1021/ja200820m  1
2011 De Rycke N, Berionni G, Couty F, Mayr H, Goumont R, David OR. Synthesis and reactivity of highly nucleophilic pyridines. Organic Letters. 13: 530-3. PMID 21186828 DOI: 10.1021/ol1029589  1
2011 Lakhdar S, Mayr H. Counterion effects in iminium-activated electrophilic aromatic substitutions of pyrroles. Chemical Communications (Cambridge, England). 47: 1866-8. PMID 21135973 DOI: 10.1039/c0cc04295a  1
2011 Horn M, Metz C, Mayr H. Electrofugalities of acceptor-substituted tritylium ions European Journal of Organic Chemistry. 6476-6485. DOI: 10.1002/ejoc.201100912  1
2011 Horn M, Mayr H. Electrophilicities of acceptor-substituted tritylium ions European Journal of Organic Chemistry. 6470-6475. DOI: 10.1002/ejoc.201100910  1
2011 Streidl N, Mayr H. Ionizing power of aprotic solvents European Journal of Organic Chemistry. 2498-2506. DOI: 10.1002/ejoc.201001700  1
2011 Mayr H. Reply to T.W. Bentley: Limitations of the s(E+N) and related equations Angewandte Chemie - International Edition. 50: 3612-3618. DOI: 10.1002/anie.201007923  1
2010 Zenz I, Mayr H, Mayer P. trans-2-(2-Nitro-1-phenyl-eth-yl)cyclo-hexa-none. Acta Crystallographica. Section E, Structure Reports Online. 66: o3136. PMID 21589437 DOI: 10.1107/S1600536810045423  1
2010 Appel R, Hartmann N, Mayr H. Scope and limitations of cyclopropanations with sulfur ylides. Journal of the American Chemical Society. 132: 17894-900. PMID 21114316 DOI: 10.1021/ja1084749  1
2010 Streidl N, Denegri B, Kronja O, Mayr H. A practical guide for estimating rates of heterolysis reactions. Accounts of Chemical Research. 43: 1537-49. PMID 21082867 DOI: 10.1021/ar100091m  1
2010 Kanzian T, Lakhdar S, Mayr H. Kinetic evidence for the formation of oxazolidinones in the stereogenic step of proline-catalyzed reactions. Angewandte Chemie (International Ed. in English). 49: 9526-9. PMID 21053224 DOI: 10.1002/anie.201004344  1
2010 Laub HA, Yamamoto H, Mayr H. Effect of the "supersilyl" group on the reactivities of allylsilanes and silyl enol ethers. Organic Letters. 12: 5206-9. PMID 20977255 DOI: 10.1021/ol102220e  1
2010 Breugst M, Mayr H. Ambident reactivities of pyridone anions. Journal of the American Chemical Society. 132: 15380-9. PMID 20942421 DOI: 10.1021/ja106962u  1
2010 Kanzian T, Mayr H. Electrophilic reactivities of azodicarboxylates. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 11670-7. PMID 20836096 DOI: 10.1002/chem.201001598  1
2010 Kanzian T, Nicolini S, De Crescentini L, Attanasi OA, Ofial AR, Mayr H. Electrophilic reactivities of 1,2-diaza-1,3-dienes. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 12008-16. PMID 20836093 DOI: 10.1002/chem.201000828  1
2010 Breugst M, Tokuyasu T, Mayr H. Nucleophilic reactivities of imide and amide anions. The Journal of Organic Chemistry. 75: 5250-8. PMID 20670031 DOI: 10.1021/jo1009883  1
2010 Appel R, Mayr H. Nucleophilic reactivities of sulfur ylides and related carbanions: comparison with structurally related organophosphorus compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 8610-4. PMID 20593449 DOI: 10.1002/chem.201001455  1
2010 Baidya M, Brotzel F, Mayr H. Nucleophilicities and Lewis basicities of imidazoles, benzimidazoles, and benzotriazoles. Organic & Biomolecular Chemistry. 8: 1929-35. PMID 20449500 DOI: 10.1039/c000965b  0.6
2010 Baidya M, Kobayashi S, Mayr H. Nucleophilicity and nucleofugality of phenylsulfinate (PhSO(2)(-)): a key to understanding its ambident reactivity. Journal of the American Chemical Society. 132: 4796-805. PMID 20225879 DOI: 10.1021/ja9102056  0.6
2010 Baidya M, Remennikov GY, Mayer P, Mayr H. SN2' versus SN2 reactivity: control of regioselectivity in conversions of Baylis-Hillman adducts. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 1365-71. PMID 19957319 DOI: 10.1002/chem.200902487  0.6
2010 Lakhdar S, Ofial AR, Mayr H. Reactivity parameters for rationalizing iminium-catalyzed reactions Journal of Physical Organic Chemistry. 23: 886-892. DOI: 10.1002/poc.1737  1
2010 Ammer J, Baidya M, Kobayashi S, Mayr H. Nucleophilic reactivities of tertiary alkylamines Journal of Physical Organic Chemistry. 23: 1029-1035. DOI: 10.1002/poc.1707  1
2010 Streidl N, Branzan R, Mayr H. Nucleophilicities and nucleofugalities of organic carbonates European Journal of Organic Chemistry. 4205-4210. DOI: 10.1002/ejoc.201000414  1
2010 Sailer CF, Fingerhut BP, Ammer J, Nolte C, Pugliesi I, Mayr H, Vivie-Riedle RD, Riedle E. The first picoseconds in the life of benzhydryl cations: Ultrafast generation and chemical reactions Optics Infobase Conference Papers 1
2009 Baidya M, Mayr H, Mayer P. Benzhydryl phenyl sulfone. Acta Crystallographica. Section E, Structure Reports Online. 65: o3224. PMID 21578931 DOI: 10.1107/S1600536809050363  0.6
2009 Baidya M, Mayr H, Mayer P. 4,4'-Bis(dimethyl-amino)benzhydryl phenyl sulfone. Acta Crystallographica. Section E, Structure Reports Online. 65: o3035. PMID 21578770 DOI: 10.1107/S160053680904642X  0.6
2009 Hampel N, Richter D, Ofial AR, Mayr H, Mayer P. 4-[4-(Dimethyl-amino)benzyl-idene]-2,6-dimethyl-cyclo-hexa-2,5-dienone. Acta Crystallographica. Section E, Structure Reports Online. 65: o2102. PMID 21577517 DOI: 10.1107/S1600536809030748  0.72
2009 Baidya M, Horn M, Zipse H, Mayr H. Organocatalytic activity of cinchona alkaloids: which nitrogen is more nucleophilic? The Journal of Organic Chemistry. 74: 7157-64. PMID 19697899 DOI: 10.1021/jo901670w  0.6
2009 Phan TB, Nolte C, Kobayashi S, Ofial AR, Mayr H. Can one predict changes from S(N)1 to S(N)2 mechanisms? Journal of the American Chemical Society. 131: 11392-401. PMID 19634906 DOI: 10.1021/ja903207b  0.72
2009 Lakhdar S, Appel R, Mayr H. How does electrostatic activation control iminium-catalyzed cyclopropanations? Angewandte Chemie (International Ed. in English). 48: 5034-7. PMID 19492379 DOI: 10.1002/anie.200900933  1
2009 Appel R, Loos R, Mayr H. Nucleophilicity parameters for phosphoryl-stabilized carbanions and phosphorus ylides: implications for Wittig and related olefination reactions. Journal of the American Chemical Society. 131: 704-14. PMID 19105684 DOI: 10.1021/ja8056216  1
2009 Kaumanns O, Appel R, Lemek T, Seeliger F, Mayr H. Nucleophilicities of the anions of arylacetonitriles and arylpropionitriles in dimethyl sulfoxide. The Journal of Organic Chemistry. 74: 75-81. PMID 19032115 DOI: 10.1021/jo802241x  1
2008 Lakhdar S, Tokuyasu T, Mayr H. Electrophilic reactivities of alpha,beta-unsaturated iminium ions. Angewandte Chemie (International Ed. in English). 47: 8723-6. PMID 18798186 DOI: 10.1002/anie.200802889  1
2008 Manolikakes G, Schade MA, Hernandez CM, Mayr H, Knochel P. Negishi cross-couplings of unsaturated halides bearing relatively acidic hydrogen atoms with organozinc reagents. Organic Letters. 10: 2765-8. PMID 18529011 DOI: 10.1021/ol8009013  1
2008 Baidya M, Mayr H. Nucleophilicities and carbon basicities of DBU and DBN. Chemical Communications (Cambridge, England). 1792-4. PMID 18379695 DOI: 10.1039/b801811a  0.6
2008 Westermaier M, Mayr H. Regio- and stereoselective ring-opening reactions of epoxides with indoles and pyrroles in 2,2,2-trifluoroethanol. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 1638-47. PMID 18064625 DOI: 10.1002/chem.200701366  0.52
2006 Lakhdar S, Westermaier M, Terrier F, Goumont R, Boubaker T, Ofial AR, Mayr H. Nucleophilic reactivities of indoles. The Journal of Organic Chemistry. 71: 9088-95. PMID 17109534 DOI: 10.1021/jo0614339  1
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