Zheng Jun Quan



  1. Wei K, Quan Z, Zhang Z, Da Y, Wang X. Copper(i) chloride promoted Csp(2)-N cross-coupling of 1,2-di(pyrimidin-2-yl) disulfides with amines: an efficient approach to obtain C2-amino functionalized pyrimidines. Org Biomol Chem. 2016;14:2395-8 pubmed publisher
    ..Central to this strategy is the conversion of disulfides into aryl- and alkyl amines by a copper-promoted chemoselective C-S bond cleavage. ..
  2. Zhang X, Wang T, Huo C, Wang X, Quan Z. Base-controlled chemoselectivity reaction of vinylanilines with isothiocyanates for synthesis of quinolino-2-thione and 2-aminoquinoline derivatives. Chem Commun (Camb). 2018;54:3114-3117 pubmed publisher
    ..Particularly interesting is that the reaction could produce the 2-aminoquinolines in the presence of K3PO4 with high selectivity. ..
  3. Wang T, Liu X, Huo C, Wang X, Quan Z. Base-catalyzed thio-lactamization of 2-(1-arylvinyl)anilines with CS2 for the synthesis of quinoline-2-thiones. Chem Commun (Camb). 2017;: pubmed publisher
    ..Compared to the known strategy in the literature, this method features the advantages like a short synthesis step and easily available starting materials. ..
  4. Hou F, Wang X, Quan Z. Efficient synthesis of esters through oxone-catalyzed dehydrogenation of carboxylic acids and alcohols. Org Biomol Chem. 2018;16:9472-9476 pubmed publisher
    ..Electron-rich and electron-deficient groups are compatible with the standard conditions and a variety of substrates are demonstrated. Moreover, the reaction could easily be adapted to typical prodrugs, drugs and gram-scale synthesis. ..
  5. Zhang X, Wang T, Liu X, Wang X, Quan Z. The solvent-controlled chemoselective construction of C-S/S-S bonds via the Michael reaction/thiol coupling of quinoline-2-thiones. Org Biomol Chem. 2019;17:2379-2383 pubmed publisher
    ..The corresponding products, generated from the reaction, presented a significant solvent-controlling effect. ..