Experimental study on the reaction pathway of α-haloacetophenones with nucleophiles: Direct substitution or carbonyl addition?

Journal of Physical Organic Chemistry

Volumn 25, Issue 8, 2012, Pages 680-685

  Katayama, Mika ^a   Sasagawa, Keita ^a   Yamataka, Hiroshi ^a  

^a RIKKYO UNIVERSITY   (Japan)

Author keywords

haloketones; borderline mechanism; carbonyl addition; kinetics; S N2; substituent

Indexed keywords

ACID HYDROLYSIS; CARBONYL ADDITION; ELECTRON-WITHDRAWING SUBSTITUENTS; EXPERIMENTAL STUDIES; HALOKETONES; MINOR PRODUCTS; PHENYL RINGS; REACTION PATHWAYS; S N2; SUBSTITUENT; SUBSTITUTION PRODUCTS; TWO-PRODUCT;

ENZYME KINETICS; ORGANIC COMPOUNDS;

ETHERS;

EID: 84863816907     PISSN: 08943230     EISSN: 10991395     Source Type: Journal    
DOI: 10.1002/poc.2901     Document Type: Article

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