Ahn, Hong Ryul Cho, Young Ae Kim, Dong-Su Chin, Jungwook Gyoung, Young-Soo Lee, Seokjoon Kang, Heonjoong Ham, Jungyeob 2024-01-20T22:02:51Z 2024-01-20T22:02:51Z 2021-09-03 2009-01-15 1523-7060 https://pubs.kist.re.kr/handle/201004/132800 Potassium organoselanyltrifluoroborates have been prepared from the corresponding dihalobenzene compounds in 56-92% yields through a facile one-pot, multicomponent reaction. The microwave-promoted Suzuki-Miyaura cross-coupling reaction of these substrates with various aryl and alkenyl bromides in the presence of 3.0 mol % of Pd(PPh3)(4) and 3.0 equiv of K2CO3 in aqueous 1,4-dioxane at 130 degrees C provided the desired compounds in 54-91% yields. English AMER CHEMICAL SOC ORGANOSELENIUM SELENIUM ARYL CHEMISTRY ALKENYL A Facile One-Pot Preparation of Organoselanyltrifluoroborates from Dihalobenzenes and Their Cross-Coupling Reaction Article 10.1021/ol8025999 1 ORGANIC LETTERS, v.11, no.2, pp.361 - 364 ORGANIC LETTERS 11 2 361 364 scie scopus 000262293500027 2-s2.0-61449186510 Chemistry, Organic Chemistry Article ORGANOSELENIUM SELENIUM ARYL CHEMISTRY ALKENYL Potassium organoselanyltrifluoroborates one-pot multicomponent reaction Suzuki&#8722 Miyaura cross-coupling reaction