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Volumn 12, Issue 22, 2014, Pages 3616-3621
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An enantioselective strategy for the total synthesis of (S)-tylophorine via catalytic asymmetric allylation and a one-pot DMAP-promoted isocyanate formation/Lewis acid catalyzed cyclization sequence
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Author keywords
[No Author keywords available]
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Indexed keywords
ALLYLATION;
CATALYSIS;
LINEAR TRANSFORMATIONS;
MATHEMATICAL TRANSFORMATIONS;
SYNTHESIS (CHEMICAL);
ALLYLIC ACETATES;
ASYMMETRIC ALLYLATION;
ASYMMETRIC TOTAL SYNTHESIS;
ENANTIOSELECTIVE;
INTRAMOLECULAR CYCLIZATIONS;
LEWIS ACID;
OXIDATION CATALYSTS;
TOTAL SYNTHESIS;
CYCLIZATION;
4-(DIMETHYLAMINE)PYRIDINE;
ALKALOID;
INDOLIZINE DERIVATIVE;
ISOCYANIC ACID DERIVATIVE;
LEWIS ACID;
PHENANTHRENE DERIVATIVE;
PHENANTHROINDOLIZIDINE;
PHENANTHROLINE DERIVATIVE;
PYRIDINE DERIVATIVE;
TYLOPHORINE;
CATALYSIS;
CHEMISTRY;
CYCLIZATION;
ORGANIC CHEMISTRY;
PROCEDURES;
STEREOISOMERISM;
SYNTHESIS;
ALKALOIDS;
CATALYSIS;
CHEMISTRY, ORGANIC;
CYCLIZATION;
INDOLIZINES;
ISOCYANATES;
LEWIS ACIDS;
PHENANTHRENES;
PHENANTHROLINES;
PYRIDINES;
STEREOISOMERISM;
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EID: 84900833063
PISSN: 14770520
EISSN: None
Source Type: Journal
DOI: 10.1039/c4ob00200h Document Type: Article |
Times cited : (21)
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References (48)
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