Ethyl lactate mediated thioacetalization of aldehydes at ambient temperature
作者:Jie-Ping Wan、Yanfeng Jing、Yunyun Liu
DOI:10.1080/10426507.2016.1209504
日期:2016.10.2
GRAPHICAL ABSTRACT ABSTRACT Dithioacetalization reactions of aldehydes with thiols/thiophenols have been successfully achieved at room temperature by employing the green, bio-basedethyllactate as the reaction medium. By means of this sustainableapproach, a class of dithioacetals has been acquired with high diversity and efficiency.
POCHAT F., TETRAHEDRON LETT., 1977, NO 43, 3813-3816
作者:POCHAT F.
DOI:——
日期:——
Cyanuric chloride-catalyzed thioacetalization for organocatalytic synthesis of thioacetals
作者:Yaqin Liu
DOI:10.1080/10426507.2015.1054934
日期:2016.5.3
GRAPHICAL ABSTRACT ABSTRACT The thioacetalization of aromatic aldehydes has been realized with broad diversity in the presence of various thiols and thiophenols using cyanuric chloride as an organocatalyst.
Synthesis of Vicinal Bis(alkylthio) Derivatives by Reductive Coupling of Dithioacetals Derived from Aromatic Aldehydes with Low Valent Titanium Iodide Species
Reduction of dithioacetals derived from aromatic aldehydes with lowvalenttitanium iodide species in situ formed by treatment of titanium(IV) iodide with zinc in a mixed solvent of dichloro-methane and pivalonitrile at room temperature afforded coupling products, vicinal bis(alkylthio) derivatives, in good to high yields.