Linked Life Data

17728855

Source:http://linkedlifedata.com/resource/pubmed/id/17728855

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
18
pubmed:dateCreated
2007-8-30
pubmed:abstractText
Highly enantioselective aldol reactions of aldehydes with cyclic ketones catalyzed by a primary amine derived from cinchonine are reported. Aromatic aldehydes reacted with various cyclic ketones cleanly to afford the anti-aldol adducts in up to 99% yield, with good diastereoselectivities (up to 9 : 1) and excellent enantioselectivities (up to 99% ee).
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Sep
pubmed:issn
1477-0520
pubmed:author
pubmed:issnType
Print
pubmed:day
21
pubmed:volume
5
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2913-5
pubmed:year
2007
pubmed:articleTitle
Highly enantioselective direct aldol reaction catalyzed by cinchona derived primary amines.
pubmed:affiliation
College of Chemistry and Chemical Engineering, China West Normal University, Nanchong, 637002, China.
pubmed:publicationType
Journal Article