Source:http://linkedlifedata.com/resource/pubmed/id/17909502
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2007-10-2
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pubmed:abstractText |
N,N,N,N-tetramethylethylenediamine (TMEDA) can be synthesized by simple reduction of 1,3,6,8-tetraazatricyclo-[4.4.1.1.(3,8)]dodecane (TATD), an aminal cage type amine, with formic acid. The aminal can be converted to TMEDA in high yield very easily and in a very short time. We comment on the scope and limitations of the reduction of this aminal and propose a possible reaction mechanism.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alkanes,
http://linkedlifedata.com/resource/pubmed/chemical/Heterocyclic Compounds, 3-Ring,
http://linkedlifedata.com/resource/pubmed/chemical/Organometallic Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Reducing Agents,
http://linkedlifedata.com/resource/pubmed/chemical/n-dodecane,
http://linkedlifedata.com/resource/pubmed/chemical/phenyllithium
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pubmed:status |
MEDLINE
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pubmed:issn |
1420-3049
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1471-81
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pubmed:dateRevised |
2009-10-27
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pubmed:meshHeading | |
pubmed:year |
2007
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pubmed:articleTitle |
Unusual reactivity patterns of 1,3,6,8-tetraazatricyclo-[4.4.1.1(3,8)]-dodecane (TATD) towards some reducing agents: synthesis of TMEDA.
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pubmed:affiliation |
Departamento de Química, Universidad Nacional de Colombia, Carrera 30 No. 45-03, Ciudad Universitaria, Bogotá, DC, Colombia. ariverau@unal.edu.co
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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