Linked Life Data

19739686

Source:http://linkedlifedata.com/resource/pubmed/id/19739686

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
18
pubmed:dateCreated
2009-9-10
pubmed:abstractText
A new and efficient samarium diiodide-promoted carbon-carbon bond fragmentation reaction of alpha-aminomethyl malonates, taking place normally at room temperature and generating the corresponding deaminomethylation products in 74-94% yields, is reported. The presence of the amino group is necessary for the success of the current transformation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1523-7052
pubmed:author
pubmed:issnType
Electronic
pubmed:day
17
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4136-8
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
SmI(2)-mediated carbon-carbon bond fragmentation in alpha-aminomethyl malonates.
pubmed:affiliation
The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, 38 Xue Yuan Road, Beijing 100083, China.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't