The effect of steric hindrance on the relative rates of anchimerically assisted alcohol eliminations from MH+ ions of 2-substituted 1,4-dialkoxybutanes upon CI and CID-Reference-Cited by-同舟云学术

The effect of steric hindrance on the relative rates of anchimerically assisted alcohol eliminations from MH+ ions of 2-substituted 1,4-dialkoxybutanes upon CI and CID

Published:2006-03 Issue: Volume:249-250 Page:433-445
ISSN:1387-3806
Container-title:International Journal of Mass Spectrometry
language:en
Short-container-title:International Journal of Mass Spectrometry

Author:

Ari Julius Ben,Navon Ilana,Mandelbaum Asher

Publisher

Elsevier BV

Subject

Physical and Theoretical Chemistry,Spectroscopy,Condensed Matter Physics,Instrumentation

Reference28 articles.

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2. 1,3-Dioxolanylium- und 1,3-Dioxanylium-Derivate via Protonenkatalysierte SNi-Reaktionen in der Gasphase

3. The isobutane chemical ionization mass spectra of 2-methyl substituted 1,3-cycloalkanediol diacetates and dimethyl ethers

4. The chemical ionization mass spectra of 2-tert-butyl-substituted 1,3-cycloalkanediol diacetates and dimethyl ethers

5. Stereochemical effects in mass spectrometry: preferential formation of bromonium ions from trans-substituted 1,1′,2,2′-polyalkyl-2,2′-dibromodiethyl ethers

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