Analysis of catecholamines in urine by positive-ion electrospray tandem mass spectrometry
Kushnir MM, Urry FM, Frank EL, Roberts WL, Shushan B. Analysis of catecholamines in urine by positive-ion electrospray tandem mass spectrometry. Clin. Chem. 2002; 48: 323.
Identification of catecholamines in the immune system by electrospray ionization and tandem mass spectrometry
Bergquist J, Silberring J. Identification of catecholamines in the immune system by electrospray ionization and tandem mass spectrometry. Rapid Commun. Mass Spectrom. 1998; 12: 683.
Fragmentation mechanisms of protonated benzylamines. Electrospray ionization-tandem mass spectrometry study and ab initio molecular orbital calculations
Bourcier S, Hoppilliard Y. Fragmentation mechanisms of protonated benzylamines. Electrospray ionization-tandem mass spectrometry study and ab initio molecular orbital calculations. Eur. J. Mass Spectrom. 2003; 9: 351.
Comparison of in vitro antifungal activities of topical antimycotics launched in 1990s in Japan
Nimura K, Niwano Y, Ishiduka S, Fukumoto R. Comparison of in vitro antifungal activities of topical antimycotics launched in 1990s in Japan. Int. J. Antimicrob. Agents 2001; 18: 173.
Stable carbocations. CXVIII. General concept and structure of carbocations based on differentiation of trivalent (classical) carbenium ions from three-center bound penta-of tetracoordinated (nonclassical) carbonium ions. Role of carbocations in electrophilic reactions
Olah GA. Stable carbocations. CXVIII. General concept and structure of carbocations based on differentiation of trivalent (classical) carbenium ions from three-center bound penta-of tetracoordinated (nonclassical) carbonium ions. Role of carbocations in electrophilic reactions. J. Am. Chem. Soc. 1972; 94: 808.
Seven-membered ring or phenyl-substituted cation? Relative stabilities of the tropylium and benzyl cations and their silicon analogues
Nicolaides A, Radom L. Seven-membered ring or phenyl-substituted cation? Relative stabilities of the tropylium and benzyl cations and their silicon analogues. J. Am. Chem. Soc. 1994; 116: 9769.
Characterization of the chemical ionization condensation products for the benzyl acetate system using mass-analyzed ion kinetic energy spectrometry
Cameron D, Cooks RG. Characterization of the chemical ionization condensation products for the benzyl acetate system using mass-analyzed ion kinetic energy spectrometry. J. Am. Chem. Soc. 1979; 101: 316.
Polycondensation of benzyl methyl ether by reaction with gaseous benzyl cations - A potpourri of mechanisms of organic ion/molecule reactions
Grützmacher H-F, Dohmeier-Fischer S. Polycondensation of benzyl methyl ether by reaction with gaseous benzyl cations - a potpourri of mechanisms of organic ion/molecule reactions. Int. J. Mass Spectrom. 1998; 179/180: 207.
Mobile protons in large gaseous alkylbenzenium ions. The 21-proton equilibration in protonated tetrabenzylmethane and related "proton dances"
Kuck D, Petersen A, Fastabend U. Mobile protons in large gaseous alkylbenzenium ions. The 21-proton equilibration in protonated tetrabenzylmethane and related "proton dances". Int. J. Mass Spectrom. 1998; 179/180: 129.
Half a century of scrambling in organic ions: Complete, incomplete, progressive and composite atom interchange
Kuck D. Half a century of scrambling in organic ions: Complete, incomplete, progressive and composite atom interchange. Int. J. Mass Spectrom. 2002; 213: 101.
Formation of gaseous π and ion-neutral complexes as probed by interannular tert-butyl cation transfer in protonated tert-butyl-substituted diphenylalkanes
Kuck D, Matthias C. Formation of gaseous π and ion-neutral complexes as probed by interannular tert-butyl cation transfer in protonated tert-butyl-substituted diphenylalkanes. J. Am. Chem. Soc. 1992; 114: 1901.