Source:http://linkedlifedata.com/resource/pubmed/id/20526506
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2010-7-29
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pubmed:abstractText |
The cycloadducts of tethered naphthalene and anthracene derivatives undergo photochemical ring opening to an electronically excited product with adiabatic yields up to 90%.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1474-9092
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1082-4
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pubmed:year |
2010
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pubmed:articleTitle |
Adiabatic ring opening in tethered naphthalene and anthracene cycloadducts.
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pubmed:affiliation |
Department of Chemistry, Columbia University, New York, NY 10027, USA.
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pubmed:publicationType |
Journal Article
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