Source:http://linkedlifedata.com/resource/pubmed/id/15128236
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2004-5-6
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pubmed:abstractText |
Protonated threonine and its allo diastereomer exhibit different proportions of collisionally activated dissociation (CAD) product ions. N-Methylation attenuates these differences. Water loss from protonated allo-threonine gives protonated trans-3-methylaziridinecarboxylic acid via an internal S(N)2 pathway, rather than protonated vinylglycine.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
May
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pubmed:issn |
1523-7060
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
13
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pubmed:volume |
6
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1561-4
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pubmed:year |
2004
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pubmed:articleTitle |
Decomposition of protonated threonine, its stereoisomers, and its homologues in the gas phase: evidence for internal backside displacement.
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pubmed:affiliation |
Department of Chemistry, University of California-Riverside, Riverside, California 92521-0403, USA.
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pubmed:publicationType |
Journal Article
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