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Volumn 11, Issue 17, 2013, Pages 2847-2858
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A stereoselective synthesis of the C9-C19 subunit of (+)-peloruside A
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Author keywords
[No Author keywords available]
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Indexed keywords
ANTI-TUMOR AGENTS;
ASYMMETRIC TRANSFER HYDROGENATION;
CHEMOENZYMATIC ROUTE;
CONTROLLED REDUCTION;
HYDROSTANNATION;
REGIO-SELECTIVE;
STEREOSELECTIVE SYNTHESIS;
VINYLOGOUS MUKAIYAMA ALDOL REACTIONS;
ALKYLATION;
CONDENSATION REACTIONS;
STEREOSELECTIVITY;
STEREOCHEMISTRY;
FUSED HETEROCYCLIC RINGS;
LACTONE;
PELORUSIDE A;
ARTICLE;
CHEMICAL STRUCTURE;
CHEMISTRY;
STEREOISOMERISM;
SYNTHESIS;
BICYCLO COMPOUNDS, HETEROCYCLIC;
LACTONES;
MOLECULAR STRUCTURE;
STEREOISOMERISM;
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EID: 84875861767
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c3ob27508f Document Type: Article |
Times cited : (11)
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References (56)
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