Construction of Optically Active Quaternary Propargyl Amines by Highly Enantioselective Zinc/BINOL-Catalyzed Alkynylation of Ketoimines [Erratum to document cited in CA159:576933] was written by Huang, Gaochao;Yin, Zengsheng;Zhang, Xingang. And the article was included in Chemistry – A European Journal in 2013.Reference of 851615-07-1 The following contents are mentioned in the article:
The CCDC numbers reported for compounds 5j, 6j, 7a, and 9 were incorrect; the corrected numbers are given and the supplementary crystallog. data can be obtained from The Cambridge Crystallog. Data Center. This study involved multiple reactions and reactants, such as (R)-[1,3′:1′,1”:3”,1”’-Quaternaphthalene]-2′,2”-diol (cas: 851615-07-1Reference of 851615-07-1).
(R)-[1,3′:1′,1”:3”,1”’-Quaternaphthalene]-2′,2”-diol (cas: 851615-07-1) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Reference of 851615-07-1
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts