化学
硼酸化
有机化学
化学合成
组合化学
生物化学
芳基
烷基
体外
作者
Ryota Sakamoto,Minami Odagi,Atsuto Izumiseki,Kaname Konuki,Kazuo Nagasawa
标识
DOI:10.1021/acs.joc.2c00744
摘要
Vinylboronic esters and allylboronic esters are well known to afford olefins by protodeboronation, and therefore homoallenylboronic esters should be similarly available as precursors for 1,3-dienes, but this strategy has not been well explored due to the limited availability of homoallenylboronic esters. Here, we describe a versatile synthesis of homoallenylboronic esters via lithiation-borylation and subsequent 1,2-rearrangement. The resulting homoallenylboronic esters were successfully converted into Z- and E-1,3-dienes by protodeboronation using Bu4NF and B(C6F5)3/PhOH, respectively.
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