Asymmetric total synthesis of Apocynaceae hydrocarbazole alkaloids (+)-deethylibophyllidine and (+)-limaspermidine

Journal of the American Chemical Society

Volumn 137, Issue 12, 2015, Pages 4267-4273

  Du, Ji Yuan ^a   Zeng, Chao ^a   Han, Xiao Jie ^a   Qu, Hu ^a   Zhao, Xian He ^a   An, Xian Tao ^a   Fan, Chun An ^a,b  

^a LANZHOU UNIVERSITY   (China)

^b Tianjin Engineering Center of Micro Nano Biomaterials and Detection Treatment Technology   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ALKALOIDS; ENANTIOSELECTIVITY; METABOLITES; NITROGEN COMPOUNDS; PRODUCT DESIGN; STEREOCHEMISTRY;

ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; ASYMMETRIC TOTAL SYNTHESIS; DESYM-METRIZATION; ENANTIOSELECTIVE; NATURAL PRODUCTS; ORGANOCATALYTIC; QUATERNARY STEREOCENTERS;

SYNTHESIS (CHEMICAL);

ALKALOID; DEETHYLIBOPHYLLIDINE; LIMASPERMIDINE; SPERMIDINE DERIVATIVE; UNCLASSIFIED DRUG; BIOLOGICAL PRODUCT; CARBAZOLE DERIVATIVE; INDOLE ALKALOID;

ALDOL REACTION; APOCYNACEAE; ARTICLE; ASYMMETRIC CATALYSIS; ASYMMETRIC SYNTHESIS; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; MICHAEL ADDITION; CATALYSIS; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

APOCYNACEAE; BIOLOGICAL PRODUCTS; CARBAZOLES; CATALYSIS; INDOLE ALKALOIDS; MODELS, MOLECULAR; STEREOISOMERISM;

EID: 84926328759     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/jacs.5b01926     Document Type: Article

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