Uetake Yuta, Isoda Motoyuki, Niwa Takashi, Hosoya Takamitsu
Chemical Biology Team, Division of Bio-Function Dynamics Imaging , RIKEN Center for Life Science Technologies (CLST) , 6-7-3 Minatojima-Minamimachi , Chuo-ku, Kobe 650-0047 , Japan.
Laboratory for Chemical Biology , RIKEN Center for Biosystems Dynamics Research (BDR) , 6-7-3 Minatojima-minamimachi , Chuo-ku, Kobe 650-0047 , Japan.
Org Lett. 2019 Jul 5;21(13):4933-4938. doi: 10.1021/acs.orglett.9b01253. Epub 2019 Jun 24.
An unexpected gem-diborylation of 2-arylvinyl sulfides with bis(pinacolato)diboron proceeded efficiently with a rhodium catalyst. A wide range of (2,2-diborylvinyl)arenes are easily synthesized by this method using readily available reagents, including the alkenyl sulfides, that are prepared from general materials in one step. Mechanistic studies indicate that the reaction proceeds from either of the stereoisomers in a stepwise manner via borylative C-S bond cleavage and subsequent dehydrogenative borylation.
铑催化剂能高效地实现2-芳基乙烯基硫醚与双(频哪醇)二硼的意外宝石二硼化反应。通过该方法,使用包括由常见原料一步制备的链烯基硫醚在内的易得试剂,能轻松合成多种(2,2-二硼乙烯基)芳烃。机理研究表明,该反应通过硼化C-S键裂解和随后的脱氢硼化以逐步方式从任意一种立体异构体进行。