Source:http://linkedlifedata.com/resource/pubmed/id/12929358
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2003-8-21
|
pubmed:abstractText |
The bicyclic core, furo[3,2-b]pyran, of the dysiherbaines has been synthesized via two routes involving the imino 1,2-Wittig rearrangement of allyl furohydroximate and the asymmetric dihydroxylation of furylpropenol derivative.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1477-0520
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
7
|
pubmed:volume |
1
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
772-4
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading | |
pubmed:year |
2003
|
pubmed:articleTitle |
A convenient route to the furopyran core of dysiherbaine.
|
pubmed:affiliation |
Kobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe 658-8558, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|