Asymmetric Total Syntheses of Aspidodasycarpine, Lonicerine, and the Proposed Structure of Lanciferine

Journal of the American Chemical Society

Volumn 138, Issue 12, 2016, Pages 3982-3985

  Li, Yong ^a,b   Zhu, Shugao ^a   Li, Jian ^a   Li, Ang ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b SHAOXING UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOIDS; CONDENSATION REACTIONS; KETONES; METABOLITES;

ALDOL CONDENSATION; ASYMMETRIC TOTAL SYNTHESIS; ASYMMETRIC TRANSFER HYDROGENATION; ELECTRON-DEFICIENT; ENANTIOSELECTIVE TOTAL SYNTHESIS; OXIDATION STATE; STEREOCENTERS;

SYNTHESIS (CHEMICAL);

ALKALOID DERIVATIVE; ALKENE; ASPIDODASYCARPINE; CARBON; INDOLE; LANCIFERINE; LONICERINE; UNCLASSIFIED DRUG; ALKALOID; LIGAND;

ALDOL REACTION; ALKYLATION; ARTICLE; ASYMMETRIC SYNTHESIS; CYCLIZATION; DRUG STRUCTURE; DRUG SYNTHESIS; ELECTRON; ENANTIOSELECTIVITY; GEOMETRY; HYDROGENATION; CHEMICAL STRUCTURE; CHEMISTRY; MOLECULAR MODEL; OXIDATION REDUCTION REACTION; STEREOISOMERISM; SYNTHESIS;

ALKALOIDS; ALKENES; CARBON; CYCLIZATION; LIGANDS; MODELS, MOLECULAR; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM;

EID: 84964335216     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.6b00764     Document Type: Article

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