Highly enantioselective arylation of aldehydes and ketones using AlArEt2(THF) as aryl sources

Journal of Organic Chemistry

Volumn 74, Issue 9, 2009, Pages 3500-3505

  Zhou, Shuangliu ^a,b   Wu, Kuo Hui ^a   Chen, Chien An ^a   Gau, Han Mou ^a  

^a NATIONAL CHUNG HSING UNIVERSITY   (Taiwan)

^b ANHUI NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION PRODUCTS; ARYLATION; ARYLATIONS; ENANTIOSELECTIVE; EXCLUSIVE-OR; H NMR SPECTRA; HIGH YIELD; OPTICALLY ACTIVE; SHORT REACTION TIME; TERTIARY ALCOHOLS; TITANIUM COMPLEXES;

ENANTIOSELECTIVITY; KETONES; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SILICON CARBIDE; TITANIUM;

ALDEHYDES;

2,2' DIHYDROXY 1,1' BINAPHTHYL; ALDEHYDE; ALUMINUM; CARBONYL DERIVATIVE; KETONE; TITANIUM;

ARTICLE; ARYLATION; ATOM; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL BOND; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME; SYNTHESIS;

ALDEHYDES; ALUMINUM; CATALYSIS; KETONES; MAGNETIC RESONANCE SPECTROSCOPY; NAPHTHOLS; ORGANOMETALLIC COMPOUNDS; STEREOISOMERISM; SUBSTRATE SPECIFICITY; TITANIUM;

EID: 66449100362     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900348p     Document Type: Article

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