Acetalization allows the photoheterolysis of the Ar-Cl bond in chlorobenzaldehydes and chloroacetophenones

Journal of Organic Chemistry

Volumn 77, Issue 20, 2012, Pages 9094-9101

  Raviola, Carlotta ^a   Protti, Stefano ^a   Ravelli, Davide ^a   Mella, Mariella ^a   Albini, Angelo ^a   Fagnoni, Maurizio ^a  

^a UNIVERSITY OF PAVIA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,3-DIOXOLANES; ACETALIZATION; AROMATIC KETONES; ARYL CHLORIDE; CARBONYL GROUPS; CARBOXYL GROUPS; PHENYL CATIONS; PHOTOACTIVATION; PHOTOHETEROLYSIS;

ALDEHYDES; CHEMICAL COMPOUNDS; CHLORINE COMPOUNDS; KETONES; POSITIVE IONS;

AROMATIC COMPOUNDS;

1,3 DIOXOLANE DERIVATIVE; ACETAL; ACETOPHENONE DERIVATIVE; ALDEHYDE DERIVATIVE; AROMATIC COMPOUND; CARBONYL DERIVATIVE; CHLORIDE; CHLOROACETOPHENONE DERIVATIVE; CHLOROBENZALDEHYDE DERIVATIVE; ESTER; ETHER; KETONE; NUCLEOPHILE; PHENYL GROUP; SILANE DERIVATIVE; SOLVENT; UNCLASSIFIED DRUG;

ACETALIZATION; ARTICLE; CHEMICAL BOND; ELECTRON; IRRADIATION; PHOTOACTIVATION; PHOTOCHEMISTRY; PHOTOHETEROLYSIS; PHOTOREACTIVITY;

ACETALS; ARGON; BENZALDEHYDES; CHLORIDES; MOLECULAR STRUCTURE; OMEGA-CHLOROACETOPHENONE; PHOTOCHEMICAL PROCESSES; QUANTUM THEORY;

EID: 84867696557     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3016264     Document Type: Article

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