A highly chemoselective and rapid chlorination of benzyl alcohols under neutral conditions

Synthesis

Volumn , Issue 24, 2008, Pages 3919-3924

  Sun, Lili ^a   Peng, Guisheng ^a   Niu, Hongmei ^a   Wang, Qiang ^a   Li, Chunbao ^a  

^a TIANJIN UNIVERSITY   (China)

Author keywords

Benzyl alcohols; Benzyl chlorides; Chemoselectivity; Halogenation; Sulfoxides

Indexed keywords

CHLORINE; CHLORINE COMPOUNDS; DIMETHYL SULFOXIDE; FUNCTIONAL GROUPS; HALOGENATION;

ALIPHATIC ALCOHOLS; BENZYL ALCOHOLS; BENZYL CHLORIDES; CHEMOSELECTIVE; CHEMOSELECTIVITY; HIGH SELECTIVITIES; INTERMOLECULAR REACTIONS; MEDICINAL CHEMISTRIES; NEUTRAL CONDITIONS; NEW TOOLS; REACTION CONDITIONS; SELECTIVE CHLORINATIONS; SULFOXIDES;

CHLORINATION;

2 [2 (CHLOROMETHYL) 4 NITROPHENOXY]ETHANOL; 2 [2 (CHLOROMETHYL)PHENOXY]ETHANOL; 2 [4 (CHLOROMETHYL) 4 METHOXYPHENOXY]ETHANOL; 2 [4 (CHLOROMETHYL)PHENOXY]ETHANOL; 2 [5 (CHLOROMETHYL) 2 METHOXYPHENOXY]ETHANOL; 4 METHOXYBENZYL CHLORIDE; ALKANOL; BENZYL ALCOHOL DERIVATIVE; DIMETHYL SULFOXIDE; FUNCTIONAL GROUP; TRIAZINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; CHLORINATION; MOLECULAR INTERACTION; REACTION TIME; SYNTHESIS;

EID: 58149355301     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0028-1083243     Document Type: Article

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