I found the field of Chemistry very interesting. Saw the article Iron-Catalyzed Regioselective Alkenylboration of Olefins published in 2021. Recommanded Product: 105-13-5, Reprint Addresses Koh, MJ (corresponding author), Natl Univ Singapore, Dept Chem, 12 Sci Dr 2, Singapore 117549, Singapore.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol
The first examples of an iron-catalyzed three-component synthesis of homoallylic boronates from regioselective union of bis(pinacolato)diboron, an alkenyl halide (bromide, chloride or fluoride), and an olefin are disclosed. Products that bear tertiary or quaternary carbon centers could be generated in up to 87 % yield as single regioisomers with complete retention of the olefin stereochemistry. With cyclopropylidene-containing substrates, ring cleavage leading to trisubstituted E-alkenylboronates were selectively obtained. Mechanistic studies revealed reaction attributes that are distinct from previously reported alkene carboboration pathways.
Welcome to talk about 105-13-5, If you have any questions, you can contact Yu, XL; Zheng, HL; Zhao, HN; Lee, BC; Koh, MJ or send Email.. Recommanded Product: 105-13-5
Reference:
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