|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
20
|
|
pubmed:dateCreated |
1999-12-23
|
|
pubmed:abstractText |
Several N-substituted 11-azaartemisinins were prepared from 11-azaartemisinin in high yield by the DMAP catalyzed addition of terminal acetylenes conjugated with electron-withdrawing groups. Their antimalarial activities against two drug-resistant strains of Plasmodium falciparum were determined.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Oct
|
|
pubmed:issn |
0960-894X
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
18
|
|
pubmed:volume |
9
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
2969-72
|
|
pubmed:dateRevised |
2003-11-14
|
|
pubmed:meshHeading |
|
|
pubmed:year |
1999
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|
pubmed:articleTitle |
Structure and antimalarial activity of adducts of 11-azaartemisinin with conjugated terminal acetylenes.
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|
pubmed:affiliation |
Israel Institute for Biological Research, Ness Ziona, Israel.
|
|
pubmed:publicationType |
Journal Article
|
