How the Structural elucidation of the natural product Stephanosporin led to new developments in aryl radical and medicinal chemistry

Synlett

Volumn 26, Issue 5, 2015, Pages 580-603

  Fehler, Stefanie K ^a   Heinrich, Markus R ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

arylations; diazonium compounds; Gomberg Bachmann reactions; hydrazines; Meerwein reactions; radical reactions

Indexed keywords

ARYLHYDRAZINE DERIVATIVE; DIAZONIUM COMPOUND; FLUORINE 18; HYDRAZINE DERIVATIVE; N ARYL N' SUCCINYLHYDRAZINE DERIVATIVE; NATURAL PRODUCT; NITRIC OXIDE; RADICAL; STEPHANOSPORIN; TITANIUM; TRIETHYLBORANE; UNCLASSIFIED DRUG;

ALLYLATION; AMINOLYSIS; ARTICLE; ARYLATION; CARBOCYANATION; CARBODIAZENYLATION; CARBOFLUORINATION; CARBONITROSATION; CARBOOXYGENATION; CHEMICAL LABELING; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; GOMBERG BACHMANN REACTION; MEDICINAL CHEMISTRY; MEERWEIN ARYLATION; NUCLEOPHILICITY; STEREOCHEMISTRY; VINYLATION;

EID: 84924149563     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0034-1378945     Document Type: Article

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