HPLC of Formula: C8H10O2. Authors Song, JL; Hua, ML; Huang, X; Visa, A; Wu, TB; Fan, HL; Hou, MQ; Zhang, ZF; Han, BX in ROYAL SOC CHEMISTRY published article about in [Song, Jinliang; Hua, Manli; Huang, Xin; Wu, Tianbin; Fan, Honglei; Hou, Minqiang; Zhang, Zhaofu; Han, Buxing] Chinese Acad Sci, CAS Key Lab Colloid & Interface & Thermodynam, CAS Res Educ Ctr Excellence Mol Sci, Beijing Natl Lab Mol Sci,Inst Chem, Beijing 100190, Peoples R China; [Hua, Manli; Huang, Xin; Han, Buxing] Univ Chinese Acad Sci, Sch Chem & Chem Engn, Beijing 100049, Peoples R China; [Visa, Aurelia] Romanian Acad, Inst Chem Timisoara, 24 M Viteazul Ave, Timisoara 300223, Romania in 2021, Cited 44. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5
The Meerwein-Ponndorf-Verley (MPV) reaction is an attractive approach to selectively reduce carbonyl groups, and the design of advanced catalysts is the key for these kinds of interesting reactions. Herein, we fabricated a novel zirconium organoborate using 1,4-benzenediboronic acid (BDB) as the precursor for MPV reduction. The prepared Zr-BDB had excellent catalytic performance for the MPV reduction of various biomass-derived carbonyl compounds (i.e., levulinate esters, aldehydes and ketones). More importantly, the number of borate groups on the ligands significantly affected the catalytic activity of the Zr-organic ligand hybrids, owing to the activation role of borate groups on hydroxyl groups in the hydrogen source. Detailed investigations revealed that the excellent performance of Zr-BDB was contributed by the synergetic effect of Zr4+ and borate. Notably, this is the first work to enhance the activity of Zr-based catalysts in MPV reactions using borate groups.
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