메뉴 건너뛰기




Volumn 299, Issue 1, 2011, Pages 13-19

Recognizing ortho-, meta- or para-positional isomers of S-methyl methoxylphenylmethylenehydrazine dithiocarboxylates by ESI-MS2: The positional effect of the methoxyl substituent

Author keywords

DFT calculation; ESI MS MS; Isomer differentiation; The positional effect of methoxyl substituent

Indexed keywords


EID: 78649449146     PISSN: 13873806     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijms.2010.09.004     Document Type: Article
Times cited : (21)

References (40)
  • 31
    • 0042697374 scopus 로고    scopus 로고
    • Quantitative high-throughput analysis of drugs in biological matrices by mass spectrometry
    • Hopfgartner G., Bourgogne E. Quantitative high-throughput analysis of drugs in biological matrices by mass spectrometry. Mass Spectrom. Rev. 2003, 22:195.
    • (2003) Mass Spectrom. Rev. , vol.22 , pp. 195
    • Hopfgartner, G.1    Bourgogne, E.2
  • 39
    • 78649443406 scopus 로고    scopus 로고
    • The relative collisional energy in this ion trap instrument (LCQ) varies from 0 to 100%, where 0-100% relative collisional energy correspond to 0-5V peak to peak of the resonance excitation RF voltage, e.g. 20% relative collisional energy means 1V (5V×20%).
    • The relative collisional energy in this ion trap instrument (LCQ) varies from 0 to 100%, where 0-100% relative collisional energy correspond to 0-5V peak to peak of the resonance excitation RF voltage, e.g. 20% relative collisional energy means 1V (5V×20%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.