Regioselectivity of intramolecular rhodium-catalyzed c-h insertion reactions of α-aryl-α-diazocarboxylates: Influence of the aryl substituent

Synlett

Volumn 25, Issue 8, 2014, Pages 1081-1084

  Wamser, Maximilian ^a   Bach, Thorsten ^a  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

carbene complexes; diastereoselectivity; insertion; lactones; regioselectivity; rhodium; ring closure

Indexed keywords

ALPA ARYL ALPHA DIAZOCARBOXYLATE; CARBENE; CARBON; CARBOXYLIC ACID DERIVATIVE; HYDROGEN; RHODIUM; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; ARYLATION; CATALYST; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; HYDROGEN BOND; PROTON NUCLEAR MAGNETIC RESONANCE; REGIOSELECTIVITY; STEREOCHEMISTRY; STEREOSPECIFICITY;

EID: 84899984505     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0033-1341062     Document Type: Article

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