Linked Life Data

21161095

Source:http://linkedlifedata.com/resource/pubmed/id/21161095

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2011-2-8
pubmed:abstractText
A new oxapalladacycle 3 can be conveniently prepared via direct ortho palladation of diphenylphosphinic acid with palladium acetate. Catalysts derived from 3 can efficiently catalyze Markovnikov-type additions of E-H bonds (P(O)-H, S-H and spC-H) to alkynes via a unique catalytic cycle.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Feb
pubmed:issn
1364-548X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
28
pubmed:volume
47
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2333-5
pubmed:year
2011
pubmed:articleTitle
A new oxapalladacycle generated via ortho C-H activation of phenylphosphinic acid: an efficient catalyst for Markovnikov-type additions of E-H bonds to alkynes.
pubmed:affiliation
National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8565, Japan.
pubmed:publicationType
Journal Article