Electron ionization mass spectrometry fragmentation pathways of trimethylsilyl derivatives of isomeric allylic alcohols derived from HBI alkene oxidation-Reference-Cited by-同舟云学术

Electron ionization mass spectrometry fragmentation pathways of trimethylsilyl derivatives of isomeric allylic alcohols derived from HBI alkene oxidation

Published:2014-08-03 Issue:17 Volume:28 Page:1937-1947
ISSN:0951-4198
Container-title:Rapid Communications in Mass Spectrometry
language:en
Short-container-title:Rapid Commun. Mass Spectrom.

Author:

Rontani Jean-François¹,Belt Simon T.²,Brown Thomas A.²,Aubert Claude³

Affiliation:

1. Aix-Marseille Université; Mediterranean Institute of Oceanography (MIO); 13288 Marseille Cedex 9; Université du Sud Toulon-Var, 83957, CNRS-INSU/IRD UM 110, France

2. Biogeochemistry Research Centre, School of Geography, Earth and Environmental Sciences; University of Plymouth; Drake Circus Plymouth PL4 8AA UK

3. Laboratoire de Pharmacocinétique et Toxicocinétique (EA 3286); Faculté de Pharmacie; 13385 Marseille France

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Analytical Chemistry

Reference19 articles.

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3. C25 and C30 highly branched isoprenoid alkenes in laboratory cultures of two marine diatoms;Volkman;Org. Geochem.,1994

4. Structural identification of the C25 highly branched isoprenoid pentaene in the marine diatom Rhizosolenia setigera;Sinninghe-Damsté;Org. Geochem.,1999

5. Highly branched isoprenoids (HBIs): Identification of the most common and abundant sedimentary isomers;Belt;Geochim. Cosmochim. Acta,2000

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