A highly efficient carbon-sulfur bond formation reaction via microwave-assisted nucleophilic substitution of thiols to polychloroalkanes without a transition-metal catalyst

Canadian Journal of Chemistry

Volumn 84, Issue 11, 2006, Pages 1529-1533

  Cao, Yi Ju ^a   Lai, Yuan Yuan ^a   Cao, Hong ^a   Xing, Xiao Ning ^a   Wang, Xiang ^a,b   Xiao, Wen Jing ^a  

^a CENTRAL CHINA NORMAL UNIVERSITY   (China)

^b Kaili College   (China)

Author keywords

Microwave; Nucleophilic substitution; Sulfide; Thiol

Indexed keywords

NUCLEOPHILIC SUBSTITUTION; THIOL;

CATALYST ACTIVITY; PARAFFINS; SUBSTITUTION REACTIONS; SYNTHESIS (CHEMICAL);

CHEMICAL BONDS;

ACETAL DERIVATIVE; ALKANE DERIVATIVE; CARBON; DICHLOROMETHANE; DITHIOACETAL DERIVATIVE; POLYCHLOROALKANE DERIVATIVE; SULFIDE; SULFUR; THIOL; THIOPHENOL; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL BINDING; CHEMICAL REACTION; CHEMICAL STRUCTURE; COLUMN CHROMATOGRAPHY; MICROWAVE RADIATION; PROTON NUCLEAR MAGNETIC RESONANCE; SUBSTITUTION REACTION;

EID: 33846955761     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/V06-151     Document Type: Article

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