Source:http://linkedlifedata.com/resource/pubmed/id/11483063
Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
16
|
| pubmed:dateCreated |
2001-8-2
|
| pubmed:abstractText |
[reaction: see text] A new method for the formation of C-glycosides has been developed employing a cationic rhodium(I)-catalyzed 1,4-addition of arylboronic acids to enones derived from glycals. The reaction is stereoselective for the alpha-anomer and is highly dependent on the nature of the rhodium catalyst.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Aug
|
| pubmed:issn |
1523-7060
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
9
|
| pubmed:volume |
3
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
2571-3
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:11483063-Acetylation,
pubmed-meshheading:11483063-Boronic Acids,
pubmed-meshheading:11483063-Catalysis,
pubmed-meshheading:11483063-Glycosides,
pubmed-meshheading:11483063-Indicators and Reagents,
pubmed-meshheading:11483063-Magnetic Resonance Spectroscopy,
pubmed-meshheading:11483063-Rhodium,
pubmed-meshheading:11483063-Stereoisomerism
|
| pubmed:year |
2001
|
| pubmed:articleTitle |
Stereoselective C-glycoside formation by a rhodium(I)-catalyzed 1,4-addition of arylboronic acids to acetylated enones derived from glycals.
|
| pubmed:affiliation |
MCR Research Inc., Chemistry and Computer Sciences Bldg., York University, 4700 Keele St., Toronto, Ontario, Canada M3J 1P3.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|