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AgSbF6-Catalyzed anti-Markovnikov hydroboration of terminal alkynes†
Chemical Communications ( IF 4.3 ) Pub Date : 2018-12-21 00:00:00 , DOI: 10.1039/c8cc07499b Ramesh Mamidala 1, 2, 3, 4 , Vipin K. Pandey 1, 2, 3, 4 , Arnab Rit 1, 2, 3, 4
Chemical Communications ( IF 4.3 ) Pub Date : 2018-12-21 00:00:00 , DOI: 10.1039/c8cc07499b Ramesh Mamidala 1, 2, 3, 4 , Vipin K. Pandey 1, 2, 3, 4 , Arnab Rit 1, 2, 3, 4
Affiliation
AgSbF6-Catalyzed anti-Markovnikov addition of pinacolborane (HBpin) to terminal alkynes to produce the E-vinylboronates is reported. This efficient methodology is scalable, compatible with sterically and electronically diverse alkynes, and works at room temperature under solvent-free condition. The utility of this method is demonstrated in the facile synthesis of the clinically important (E)-2,4,3′,5′-tetramethoxystilbene.
中文翻译:
AgSbF 6-末端炔烃的催化反马氏水硼化†
报道了在末端炔烃中AgSbF 6-催化的潘可可硼烷(HBpin)的抗-Markovnikov加成以产生E-乙烯基硼酸酯。这种有效的方法是可扩展的,可与空间和电子多样化的炔烃兼容,并且可在室温下于无溶剂条件下工作。该方法的实用性在临床上很重要的(E)-2,4,3',5'-四甲氧基sti的简便合成中得到了证明。
更新日期:2018-12-21
中文翻译:
AgSbF 6-末端炔烃的催化反马氏水硼化†
报道了在末端炔烃中AgSbF 6-催化的潘可可硼烷(HBpin)的抗-Markovnikov加成以产生E-乙烯基硼酸酯。这种有效的方法是可扩展的,可与空间和电子多样化的炔烃兼容,并且可在室温下于无溶剂条件下工作。该方法的实用性在临床上很重要的(E)-2,4,3',5'-四甲氧基sti的简便合成中得到了证明。