sp3 C-H bond arylation directed by amidine protecting group: α-arylation of pyrrolidines and piperidines

Journal of the American Chemical Society

Volumn 128, Issue 44, 2006, Pages 14220-14221

  Pastine, Stefan J ^a   Gribkov, Denis V ^a   Sames, Dalibor ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMIDINE; PIPERIDINE DERIVATIVE; PYRROLIDINE DERIVATIVE; AROMATIC HYDROCARBON; CARBON; HYDROGEN;

ALKYLATION; ARTICLE; ARYLATION; CATALYST; ELIMINATION REACTION; HYDROGEN BOND; ISOMERIZATION; QUANTUM YIELD; REACTION ANALYSIS; STEREOCHEMISTRY; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM;

AMIDINES; CARBON; HYDROCARBONS, AROMATIC; HYDROGEN; MOLECULAR STRUCTURE; PIPERIDINES; PYRROLIDINES; STEREOISOMERISM;

EID: 33750720318     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja064481j     Document Type: Article

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23. Preliminary experiments suggest that similar yields may be achieved in shorter reaction times (<1 h) in a microwave reactor.