Regioselective chlorination of phenols with alumina-supported copper(II) chloride.
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چکیده
منابع مشابه
Regioselective Enzymatic Carboxylation of Bioactive (Poly)phenols
In order to extend the applicability of the regioselective enzymatic carboxylation of phenols, the substrate scope of o-benzoic acid (de)carboxylases has been investigated towards complex molecules with an emphasis on flavouring agents and polyphenols possessing antioxidant properties. o-Hydroxycarboxylic acid products were obtained with perfect regioselectivity, in moderate to excellent yields...
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Cu-mediated C-2 chlorination of indoles was accomplished with copper(ii) chloride through the use of a directing pyrimidyl protection group. A highly regioselective manner can be achieved on a range of indole substrates with excellent functional group tolerance.
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The enzymatic carboxylation of phenol and styrene derivatives using (de)carboxylases in carbonate buffer proceeded in a highly regioselective fashion: Benzoic acid (de)carboxylases selectively formed o-hydroxybenzoic acid derivatives, phenolic acid (de)carboxylases selectively acted at the β-carbon atom of styrenes forming (E)-cinnamic acids.
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Introduction of chlorine into aromatic rings by electrophilic substitution is an important synthetic transformation because chlorinated hydrocarbons are recognized as versatile starting materials and additives in th e p rod uctio n o f h igh qu ality in sectic ides, fungicides, herbicides, dyes, pharmaceuticals 1 Moreover, they can serve as precursors for numerous functionalities, such as pheno...
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ژورنال
عنوان ژورنال: NIPPON KAGAKU KAISHI
سال: 1987
ISSN: 2185-0925,0369-4577
DOI: 10.1246/nikkashi.1987.1753