SmI2-mediated radical coupling strategy to securinega alkaloids: Total synthesis of (-)-14,15-dihydrosecurinine and formal total synthesis of (-)-securinine

Journal of Organic Chemistry

Volumn 80, Issue 2, 2015, Pages 1034-1041

  Zheng, Xiao ^a,b   Liu, Juan ^a   Ye, Chen Xi ^a   Wang, Ao ^a   Wang, Ai E ^a   Huang, Pei Qiang ^a  

^a XIAMEN UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ORGANIC COMPOUNDS;

ASYMMETRIC TOTAL SYNTHESIS; DIASTEREO-SELECTIVITY; RADICAL COUPLING; SECURININE; TOTAL SYNTHESIS;

SYNTHESIS (CHEMICAL);

14,15 DIHYDROSECURININE; ALKALOID; ALPHA HYDROXY 6 AZABICYCLO [3 2 1] OCTANONE; AZABICYCLO DERIVATIVE; SECURININE; UNCLASSIFIED DRUG; ALPHA-HYDROXY 6-AZABICYCLO(3.2.1)OCTANONE; AZEPINE DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; FUSED HETEROCYCLIC RINGS; LACTONE; PIPERIDINE DERIVATIVE;

ARTICLE; ASYMMETRIC SYNTHESIS; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; CYCLIZATION; ENANTIOSELECTIVITY; STEREOCHEMISTRY; CHEMISTRY; EUPHORBIACEAE; STEREOISOMERISM; SYNTHESIS;

ALKALOIDS; AZABICYCLO COMPOUNDS; AZEPINES; EUPHORBIACEAE; HETEROCYCLIC COMPOUNDS, BRIDGED-RING; INDICATORS AND REAGENTS; LACTONES; PIPERIDINES; STEREOISOMERISM;

EID: 84921342563     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo502522x     Document Type: Article

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