%0 Journal Article
%T Oxone-Mediated Preparation of Ester Derivatives Using Indium(III) Triflate and Various Alcohols
%A Tomoko Mineno
%A Daiki Takano
%A Saika Komiya
%A Azusa Sato
%A Hisao Kansui
%J Green and Sustainable Chemistry
%P 1-8
%@ 2160-696X
%D 2022
%I Scientific Research Publishing
%R 10.4236/gsc.2022.121001
%X Esters are known as one of the most fundamental chemical
moieties and also essentially useful components<span style=\"font-size:10.0pt;font-family:;\" \"=\"\">,</span><span style=\"font-size:10.0pt;font-family:;\" \"=\"\"> especially for medicinal agents. Herein, using benzaldehyde and its
derivatives as starting materials, Oxone-mediated prepara<span>tion of ester derivatives in the presence of </span></span><span style=\"font-size:10.0pt;font-family:;\" \"=\"\">a </span><span style=\"font-size:10.0pt;font-family:;\" \"=\"\">catalytic amount of indiu</span><span style=\"font-size:10.0pt;font-family:;\" \"=\"\">m(III) triflate is
described. Alcohols with various chain length</span><span style=\"font-size:10.0pt;font-family:;\" \"=\"\">s</span><span style=\"font-size:10.0pt;font-family:;\" \"=\"\">, which functioned as solvents and substrates, were examined. Overall,
the oxidative esterification <span>starting with
benzaldehyde derivatives possessing electron withdrawing groups </span>proceeded
smoothly and gave sufficient yields, in comparison to the reactions with the
derivatives having electron donating groups.</span>
%K Oxone
%K Oxidative Esterification
%K Benzaldehyde Derivatives
%K Ester Derivatives
%K Indium(III) Triflate
%K Alcohols
%U http://www.scirp.org/journal/PaperInformation.aspx?PaperID=115268