Linked Life Data

17305351

Source:http://linkedlifedata.com/resource/pubmed/id/17305351

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2007-3-8
pubmed:abstractText
The enantioselective Brønsted acid catalyzed addition of methyleneaminopyrrolidine to N-Boc imines has been achieved in the presence of chiral phosphoric acids derived from 3,3'-di(phenanthryl)-H8-BINOL. The corresponding aminohydrazones have been isolated in good yields with enantiomeric excesses up to 90%. [reaction: see text]
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Mar
pubmed:issn
1523-7060
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1065-8
pubmed:year
2007
pubmed:articleTitle
An enantioselective chiral Brønsted acid catalyzed imino-azaenamine reaction.
pubmed:affiliation
Degussa Endowed Professorship, Institute of Chemistry and Chemical Biology, Johann-Wolfgang Goethe University Frankfurt am Main, Max-von-Laue Strasse 7, D-60438 Frankfurt, Germany. m.rueping@chemie.uni-frankfurt.de
pubmed:publicationType
Journal Article