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16805566
Source:
http://linkedlifedata.com/resource/pubmed/id/16805566
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0002062
,
umls-concept:C0021236
,
umls-concept:C0025663
,
umls-concept:C0220781
,
umls-concept:C1872026
,
umls-concept:C1883254
,
umls-concept:C1948027
,
umls-concept:C2603343
pubmed:issue
14
pubmed:dateCreated
2006-6-29
pubmed:abstractText
[reaction: see text] The two novel bisindole alkaloid structures shown can be synthesized in a few steps from the canthiphytine derivative 9.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Indole Alkaloids
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1523-7060
pubmed:author
pubmed-author:CoreyE JEJ
,
pubmed-author:RegePankaj DPD
,
pubmed-author:TianYuanY
pubmed:issnType
Print
pubmed:day
6
pubmed:volume
8
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3117-20
pubmed:meshHeading
pubmed-meshheading:16805566-Apocynaceae
,
pubmed-meshheading:16805566-Crystallography, X-Ray
,
pubmed-meshheading:16805566-Indole Alkaloids
,
pubmed-meshheading:16805566-Molecular Conformation
,
pubmed-meshheading:16805566-Molecular Structure
,
pubmed-meshheading:16805566-Nuclear Magnetic Resonance, Biomolecular
,
pubmed-meshheading:16805566-Plants, Medicinal
pubmed:year
2006
pubmed:articleTitle
Studies of new indole alkaloid coupling methods for the synthesis of haplophytine.
pubmed:affiliation
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
pubmed:publicationType
Journal Article