Source:http://linkedlifedata.com/resource/pubmed/id/17443870
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2007-4-25
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pubmed:abstractText |
The HCN-tetramer, a 'classic' of the prebiotic chemistry of HCN, is shown to undergo a remarkable reaction with acetaldehyde in slightly basic or neutral aqueous solution at room temperature. The reaction consists in an aldolization-type C,C-bond formation, accompanied by a (presumably aldehyde-catalyzed) hydration of one of the two nitrile groups and the formation of two cyclic aminal-type groupings, each of the latter incorporating an additional molecule of the aldehyde. Should this so far unexplored type of chemistry of the HCN-tetramer prove to have some generality, the finding might add a new dimension to the potential etiological relevance of this HCN-oligomer.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1612-1880
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
541-53
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pubmed:meshHeading | |
pubmed:year |
2007
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pubmed:articleTitle |
Reactions of the HCN-tetramer with aldehydes.
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pubmed:affiliation |
Laboratory of Organic Chemistry, Swiss Federal Institute of Technology ETH, Hönggerberg HCI, Wolfgang-Pauli-Strasse 10, CH-8093 Zürich.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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