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Volumn 63, Issue 51, 2007, Pages 12740-12746
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Synthesis of the octahydroindole unit of aeruginosins via asymmetric hydrogenation of the Diels-Alder adducts of 2-amido-2,4-pentadienoate
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Author keywords
[No Author keywords available]
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Indexed keywords
2 AMIDO 2,4 PENTADIENOATE;
INDOLE DERIVATIVE;
METHYL 2 ACETAMIDO 2,4 PENTADIENOATE DERIVATIVE;
OCTAHYDROINDOLE;
UNCLASSIFIED DRUG;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
CYCLIZATION;
DIELS ALDER REACTION;
HYDROGENATION;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
STEREOCHEMISTRY;
SYNTHESIS;
ALNUS;
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EID: 35748978556
PISSN: 00404020
EISSN: None
Source Type: Journal
DOI: 10.1016/j.tet.2007.09.078 Document Type: Article |
Times cited : (7)
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References (32)
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