On April 4, 2014, Jefferies, Latisha R.; Cook, Silas P. published an article.Product Details of 35444-44-1 The title of the article was Iron-Catalyzed Arene Alkylation Reactions with Unactivated Secondary Alcohols. And the article contained the following:
A simple, iron-based catalytic system allows for the inter- and intramol. arylation of unactivated secondary alcs. This transformation expands the substrate scope beyond the previously required activated alcs. and proceeds under mild reaction conditions, tolerating air and moisture. Furthermore, the use of an enantioenriched secondary alc. provides an enantioenriched product for the intramol. reaction, thereby offering a convenient approach to nonracemic products. The experimental process involved the reaction of Methyl 6-chloro-6-oxohexanoate(cas: 35444-44-1).Product Details of 35444-44-1
The Article related to unactivated secondary alc iron catalyzed intermol intramol arylation, enantioenriched secondary alc intramol iron catalyzed arylation stereoselective, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Hydrocarbons (Saturated and Unsaturated Side Chains) and other aspects.Product Details of 35444-44-1
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics