18830467

Source:http://linkedlifedata.com/resource/pubmed/id/18830467

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0282563, umls-concept:C0439810, umls-concept:C1872295, umls-concept:C1883254
pubmed:issue	39
pubmed:dateCreated	2008-10-2
pubmed:abstractText	A concise total synthesis of the antiproliferative macrolide (+)-neopeltolide has been completed, utilising a Jacobsen hetero Diels-Alder reaction to install the trisubstituted tetrahydropyran ring.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Macrolides, http://linkedlifedata.com/resource/pubmed/chemical/neopeltolide
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1359-7345
pubmed:author	pubmed-author:MillerNatalie ANA, pubmed-author:PatersonIanI
pubmed:issnType	Print
pubmed:day	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	4708-10
pubmed:meshHeading	pubmed-meshheading:18830467-Animals, pubmed-meshheading:18830467-Macrolides, pubmed-meshheading:18830467-Molecular Conformation, pubmed-meshheading:18830467-Porifera, pubmed-meshheading:18830467-Stereoisomerism
pubmed:year	2008
pubmed:articleTitle	Total synthesis of the marine macrolide (+)-neopeltolide.
pubmed:affiliation	University Chemical Laboratory, Lensfield Road, Cambridge, UK CB2 1EW. ip100@cam.ac.uk
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't