Collosional activation spectra of Li+ and Na+ cationized Diels-Alder adducts of substitutedp-benzoquinones and glucofuranodienes
Author:
Publisher
Wiley
Subject
Spectroscopy,Instrumentation,Molecular Medicine,Biochemistry
Reference10 articles.
1. Diels-Alder reaction of in-situ generated 2-methoxycarbonyl-p-quinone with D-glucose based dienes: A new approach to forskolin
2. Dual participation of generated--benzoquinones with substituted furanoid vinyl glycals in cycloaddition reaction
3. Insect antifeedants. 1. Diels-Alders approach to the synthesis of ajugarin I
4. Control of lithium aluminum hydride reduction of cyclic dicarboxylic acid anhydrides to produce .gamma.-lactones or diols
5. Diacetone glucose-derived dienes in Diels-Alder reactions. Products and transformations
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1. Fast atom bombardment mass spectral analysis of three new oxidative products of primaquine;International Journal of Mass Spectrometry;2004-03
2. Structural analysis of rapamycin and related compounds using [M + Li]+ ions generated by liquid secondary ion mass spectrometry;Organic Mass Spectrometry;1994-08
3. Structural Elucidation of Acetogenins from Annonaceae by Fast Atom Bombardment Mass Spectrometry;Tetrahedron;1994-01
4. Stereospecific Retro-Diels-Alder reactions in the negative-ion mass spectra of Diels-Alder adducts of substitutedp-benzoquinones and glucofuranodienes;Rapid Communications in Mass Spectrometry;1993-01
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