Cu-catalyzed cross-coupling reactions of vinyl epoxide with organoboron compounds: access to homoallylic alcohols was written by Lu, Xiao-Yu;Li, Jin-Song;Wang, Jin-Yu;Wang, Shi-Qun;Li, Yue-Ming;Zhu, Yu-Jing;Zhou, Ran;Ma, Wen-Jing. And the article was included in RSC Advances in 2018.SDS of cas: 1003858-50-1 The following contents are mentioned in the article:
Copper-catalyzed cross-coupling reactions of vinyl epoxide with arylboronates to obtain aryl-substituted homoallylic alcs. were described. The reaction selectivity was different to that of previously reported vinyl epoxide ring-opening reactions using aryl nucleophiles. The reaction proceeded under mild conditions, affording aryl-substituted homoallylic alcs. with high selectivity and in good to excellent yields. The reaction provided convenient access to aryl-substituted homoallylic alcs. from vinyl epoxide. This study involved multiple reactions and reactants, such as 2-(3-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane (cas: 1003858-50-1SDS of cas: 1003858-50-1).
2-(3-Methoxyphenyl)-5,5-dimethyl-1,3,2-dioxaborinane (cas: 1003858-50-1) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.SDS of cas: 1003858-50-1
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem