메뉴 건너뛰기




Volumn 14, Issue 4, 2003, Pages 289-294

Mass spectrometric study of some protonated and lithiated 2,5-disubstituted-1,3,4-oxadiazoles

Author keywords

[No Author keywords available]

Indexed keywords

DERIVATIVES; MASS SPECTROMETRY; MOLECULES; POSITIVE IONS;

EID: 0038038641     PISSN: 10440305     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1044-0305(03)00005-9     Document Type: Article
Times cited : (10)

References (26)
  • 1
    • 0031239743 scopus 로고    scopus 로고
    • Tandem Mass Spectrometry of Alkali Cationized Polysaccharides in a Quadrupole Ion Trap
    • Asam M.R., Glish G.L. Tandem Mass Spectrometry of Alkali Cationized Polysaccharides in a Quadrupole Ion Trap. J. Am. Soc. Mass Spectrom. 8:1997;987-995.
    • (1997) J. Am. Soc. Mass Spectrom. , vol.8 , pp. 987-995
    • Asam, M.R.1    Glish, G.L.2
  • 2
    • 0030745516 scopus 로고    scopus 로고
    • Effect on Lithium Cationization on Oxygen Atom Transfer from the Nitro Group to the Double Bond During Collision-Induced Decomposition in Certain Substituted β-Nitrostyrenes
    • Madhusudanan K.P., Bajpai L.K., Bhaduri A.P. Effect on Lithium Cationization on Oxygen Atom Transfer from the Nitro Group to the Double Bond During Collision-Induced Decomposition in Certain Substituted β-Nitrostyrenes. Rapid Commun. Mass Spectrom. 11:1997;1263-1265.
    • (1997) Rapid Commun. Mass Spectrom. , vol.11 , pp. 1263-1265
    • Madhusudanan, K.P.1    Bajpai, L.K.2    Bhaduri, A.P.3
  • 4
    • 0031983274 scopus 로고    scopus 로고
    • Elimination of Neutral Lithium Atom from Lithiated Nucleobases Upon Collision-Induced Decomposition
    • Madhusudanan K.P., Katti S.B. Elimination of Neutral Lithium Atom from Lithiated Nucleobases Upon Collision-Induced Decomposition. J. Mass Spectrom. 33:1998;20-24.
    • (1998) J. Mass Spectrom. , vol.33 , pp. 20-24
    • Madhusudanan, K.P.1    Katti, S.B.2
  • 5
    • 0033451330 scopus 로고    scopus 로고
    • Distinction Among Isomeric Unsaturated Fatty Acids as Lithiated Adducts by Electrospray Ionization Mass Spectrometry Using Low Energy Collisionally Activated Dissociation on a Triple Stage Quadrupole Instrument
    • Hsu F.F., Turk J. Distinction Among Isomeric Unsaturated Fatty Acids as Lithiated Adducts by Electrospray Ionization Mass Spectrometry Using Low Energy Collisionally Activated Dissociation on a Triple Stage Quadrupole Instrument. J. Am. Soc. Mass Spectrom. 10:1999;600-612.
    • (1999) J. Am. Soc. Mass Spectrom. , vol.10 , pp. 600-612
    • Hsu, F.F.1    Turk, J.2
  • 6
    • 0034614305 scopus 로고    scopus 로고
    • Multistep Collisionally Activated Decomposition in an Ion Trap for the Determination of the Amino Acid Sequence and Gas-Phase Ion Chemistry of Lithium-Coordinated Valinomycin
    • Ngoka L.C.M., Gross M.L. Multistep Collisionally Activated Decomposition in an Ion Trap for the Determination of the Amino Acid Sequence and Gas-Phase Ion Chemistry of Lithium-Coordinated Valinomycin. Int. J. Mass Spectrom. 194:2000;247-259.
    • (2000) Int. J. Mass Spectrom. , vol.194 , pp. 247-259
    • Ngoka, L.C.M.1    Gross, M.L.2
  • 7
    • 0032232019 scopus 로고    scopus 로고
    • Formation of Lithiated Adducts of Glyceroposphoholine Lipids Facilitates Their Identification by Electrospray Ionization Tandem Mass Spectrometry
    • Hsu F.F., Bohrer A., Turk J. Formation of Lithiated Adducts of Glyceroposphoholine Lipids Facilitates Their Identification by Electrospray Ionization Tandem Mass Spectrometry. J. Am. Soc. Mass Spectrom. 9:1998;516-526.
    • (1998) J. Am. Soc. Mass Spectrom. , vol.9 , pp. 516-526
    • Hsu, F.F.1    Bohrer, A.2    Turk, J.3
  • 8
    • 0032988111 scopus 로고    scopus 로고
    • Electrospray Ionization Multiple-Stage Tandem Mass Spectrometric Analysis of Diglycosyldiacylglycerol Glycolipids from the Bacteria
    • Wang W., Liu Z., Ma L., Hao C., Liu S., Voinov V.G., Kalinovskaya N.I. Electrospray Ionization Multiple-Stage Tandem Mass Spectrometric Analysis of Diglycosyldiacylglycerol Glycolipids from the Bacteria. Bacillus pumilus. Rapid Commun. Mass Spectrom. 12:1999;1189-1196.
    • (1999) Bacillus pumilus. Rapid Commun. Mass Spectrom. , vol.12 , pp. 1189-1196
    • Wang, W.1    Liu, Z.2    Ma, L.3    Hao, C.4    Liu, S.5    Voinov, V.G.6    Kalinovskaya, N.I.7
  • 9
    • 0035566770 scopus 로고    scopus 로고
    • Structural Determination of Glycosphingolipids as Lithiated Adducts by Electrospray Ionization Mass Spectrometry Using Low Energy Collision-Activated Dissociation on a Triple Stage Quadrupole Instrument
    • Hsu F.F., Turk J. Structural Determination of Glycosphingolipids as Lithiated Adducts by Electrospray Ionization Mass Spectrometry Using Low Energy Collision-Activated Dissociation on a Triple Stage Quadrupole Instrument. J. Am. Soc. Mass Spectrom. 12:2001;61-79.
    • (2001) J. Am. Soc. Mass Spectrom. , vol.12 , pp. 61-79
    • Hsu, F.F.1    Turk, J.2
  • 11
    • 0033926342 scopus 로고    scopus 로고
    • Effect of Metal Cationization on the Low Energy Collision-Induced Dissociation of Loganin, epi-Loganin, and Ketologanin Studied by Electrospray Ionization Tandem Mass Spectrometry
    • Madhusudanan K.P., Raj K., Bhaduri A.P. Effect of Metal Cationization on the Low Energy Collision-Induced Dissociation of Loganin, epi-Loganin, and Ketologanin Studied by Electrospray Ionization Tandem Mass Spectrometry. J. Mass Spectrom. 35:2000;901-911.
    • (2000) J. Mass Spectrom. , vol.35 , pp. 901-911
    • Madhusudanan, K.P.1    Raj, K.2    Bhaduri, A.P.3
  • 13
    • 0035028644 scopus 로고    scopus 로고
    • Metal Ion Adducts in the Structural Analysis of Ginsenosides by Electrospray Ionization with Multi-Stage Mass Spectrometry
    • Cui M., Song F., Liu Z., Liu S. Metal Ion Adducts in the Structural Analysis of Ginsenosides by Electrospray Ionization with Multi-Stage Mass Spectrometry. Rapid Commun. Mass Spectrom. 15:2001;586-595.
    • (2001) Rapid Commun. Mass Spectrom. , vol.15 , pp. 586-595
    • Cui, M.1    Song, F.2    Liu, Z.3    Liu, S.4
  • 14
    • 0035564259 scopus 로고    scopus 로고
    • Lithium and Transition Metal Ions Enable Low Energy Collision-Induced Dissociation of Polyglycols in Electrospray Ionization Mass Spectrometry
    • Chen R., Li L. Lithium and Transition Metal Ions Enable Low Energy Collision-Induced Dissociation of Polyglycols in Electrospray Ionization Mass Spectrometry. J. Am. Soc. Mass Spectrom. 12:2001;832-839.
    • (2001) J. Am. Soc. Mass Spectrom. , vol.12 , pp. 832-839
    • Chen, R.1    Li, L.2
  • 15
    • 0036615735 scopus 로고    scopus 로고
    • Structural Studies on Ceramides as Lithiated Adducts by Low Energy Collision-Activated Dissociation Tandem Mass Spectrometry
    • Hsu F.F., Turk J., Stewart M.E., Downing D.T. Structural Studies on Ceramides as Lithiated Adducts by Low Energy Collision-Activated Dissociation Tandem Mass Spectrometry. J. Am. Soc. Mass Spectrom. 13:2002;680-695.
    • (2002) J. Am. Soc. Mass Spectrom. , vol.13 , pp. 680-695
    • Hsu, F.F.1    Turk, J.2    Stewart, M.E.3    Downing, D.T.4
  • 16
    • 0034798970 scopus 로고    scopus 로고
    • Gas-Phase Conversion of Tetrazoles to Oxadiazoles: Isolation and Acetylation of the N-Acylated Intermediate
    • Seldes A.M.D.', Accorso N., Souto M.F., Alho M.M., Arabehety C.G. Gas-Phase Conversion of Tetrazoles to Oxadiazoles Isolation and Acetylation of the N-Acylated Intermediate . J. Mass Spectrom. 36:2001;1069-1073.
    • (2001) J. Mass Spectrom. , vol.36 , pp. 1069-1073
    • Seldes A.M.D.'1    Accorso, N.2    Souto, M.F.3    Alho, M.M.4    Arabehety, C.G.5
  • 17
    • 0036179107 scopus 로고    scopus 로고
    • Loss of Isocyanic Acid from the Internal Oxadiazole Ring of Protonated Molecules of Some 2,5-Diaryl-1,3,4-Oxadiazoles
    • Frański R., Schroeder G., Rybachenko V., Szwajka O.P. Loss of Isocyanic Acid from the Internal Oxadiazole Ring of Protonated Molecules of Some 2,5-Diaryl-1,3,4-Oxadiazoles. Rapid Commun. Mass Spectrom. 16:2002;390-395.
    • (2002) Rapid Commun. Mass Spectrom. , vol.16 , pp. 390-395
    • Frański, R.1    Schroeder, G.2    Rybachenko, V.3    Szwajka, O.P.4
  • 18
    • 0030272255 scopus 로고    scopus 로고
    • Synthesis and Insecticidal Activities of Novel 2,5-Disubstituted-1,3,4-Oxadiazoles
    • Qiang X., Zhang R. Synthesis and Insecticidal Activities of Novel 2,5-Disubstituted-1,3,4-Oxadiazoles. J. Chem. Technol. Biotechnol. 67:1996;124-130.
    • (1996) J. Chem. Technol. Biotechnol. , vol.67 , pp. 124-130
    • Qiang, X.1    Zhang, R.2
  • 19
    • 0033858143 scopus 로고    scopus 로고
    • Synthesis and Evaluation of Antimitotic Activity of Alkylated 2-Amino-1,3,4-Oxadiazoles. II
    • Rai K.M.L., Linganna N. Synthesis and Evaluation of Antimitotic Activity of Alkylated 2-Amino-1,3,4-Oxadiazoles. II. Farmaco. 55:2000;389-392.
    • (2000) Farmaco , vol.55 , pp. 389-392
    • Rai, K.M.L.1    Linganna, N.2
  • 20
    • 0034748113 scopus 로고    scopus 로고
    • Synthesis and Biological Activities of Novel Diheterocyclic Compounds Containing 1,2,4,-Triazolo[1,5-α]Pyrimidine and 1,3,4-Oxadiazole
    • Liu Z., Yang G., Qin X. Synthesis and Biological Activities of Novel Diheterocyclic Compounds Containing 1,2,4,-Triazolo[1,5-α]Pyrimidine and 1,3,4-Oxadiazole. J. Chem. Technol. Biotechnol. 76:2001;1154-1158.
    • (2001) J. Chem. Technol. Biotechnol. , vol.76 , pp. 1154-1158
    • Liu, Z.1    Yang, G.2    Qin, X.3
  • 21
    • 0035138869 scopus 로고    scopus 로고
    • Synthesis and Quantitative Structure-Activity Relationships of New 2,5-Disubstituted-1,3,4-Oxadiazoles
    • Shi W., Qian X., Zhang R., Song G. Synthesis and Quantitative Structure-Activity Relationships of New 2,5-Disubstituted-1,3,4-Oxadiazoles. J. Agri. Food Chem. 49:2001;124-130.
    • (2001) J. Agri. Food Chem. , vol.49 , pp. 124-130
    • Shi, W.1    Qian, X.2    Zhang, R.3    Song, G.4
  • 22
    • 0033661951 scopus 로고    scopus 로고
    • Synthesis and Fungicidal Activity Against Rhizoctonia solani of 2-Alkyl (Alkylthio)-5-Pyrazolyl-1,3,4-Oxadiazoles (Thiadiazoles)
    • Chen H., Li Z., Han Y. Synthesis and Fungicidal Activity Against Rhizoctonia solani of 2-Alkyl (Alkylthio)-5-Pyrazolyl-1,3,4-Oxadiazoles (Thiadiazoles). J. Agri. Food Chem. 48:2000;5312-5315.
    • (2000) J. Agri. Food Chem. , vol.48 , pp. 5312-5315
    • Chen, H.1    Li, Z.2    Han, Y.3
  • 23
    • 0000916237 scopus 로고    scopus 로고
    • Novel Syntheses of Symmetrical 2,5-Diaryl-1,3,4-Oxadiazoles and 1,4-Phenylenebis-1,3,4-Oxadiazoles
    • Belen'kii L.I., Luiksaar S.I., Poddubnyi I.S., Krayushkin M.M. Novel Syntheses of Symmetrical 2,5-Diaryl-1,3,4-Oxadiazoles and 1,4-Phenylenebis-1,3,4-Oxadiazoles. Izv. Akad. Nauk Ser. Khim. 11:1998;2309-2315.
    • (1998) Izv. Akad. Nauk Ser. Khim. , vol.11 , pp. 2309-2315
    • Belen'kii, L.I.1    Luiksaar, S.I.2    Poddubnyi, I.S.3    Krayushkin, M.M.4
  • 24
    • 0037204268 scopus 로고    scopus 로고
    • A New Class of Organosoluble Rigid-Rod Fully Aromatic Poly(1,3,4-Oxadiazole)s and Their Solid State Properties. 1. Synthesis
    • Janietz S., Anlaouf S. A New Class of Organosoluble Rigid-Rod Fully Aromatic Poly(1,3,4-Oxadiazole)s and Their Solid State Properties. 1. Synthesis. Macromol. Chem. Phys. 203:2002;427-432.
    • (2002) Macromol. Chem. Phys. , vol.203 , pp. 427-432
    • Janietz, S.1    Anlaouf, S.2
  • 25
    • 0037543602 scopus 로고
    • Synthesis of Some 2,5-Diphenyl-1,3,4-Oxadizoles
    • (in Russian)
    • Grekov A.P., Szwajka O.P. Synthesis of Some 2,5-Diphenyl-1,3,4-Oxadizoles. Zh. Obshch. Khim. 30:1960;3082-3086. (in Russian).
    • (1960) Zh. Obshch. Khim , vol.30 , pp. 3082-3086
    • Grekov, A.P.1    Szwajka, O.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.