Tracz Andrzej, Matczak Mateusz, Urbaniak Katarzyna, Skowerski Krzysztof
Apeiron Synthesis SA, Duńska 9, 54-427 Wrocław, Poland ; Department of Bioorganic Chemistry, Faculty of Chemistry, Wroclaw University of Technology, Wybrzeże Wyspańskiego 27, 50-370 Wrocław, Poland.
Apeiron Synthesis SA, Duńska 9, 54-427 Wrocław, Poland.
Beilstein J Org Chem. 2015 Oct 6;11:1823-32. doi: 10.3762/bjoc.11.198. eCollection 2015.
Iodide-containing nitro-Grela-type catalysts have been synthesized and applied to ring closing metathesis (RCM) and cross metathesis (CM) reactions. These new catalysts have exhibited improved efficiency in the transformation of sterically, non-demanding alkenes. Additional steric hindrance in the vicinity of ruthenium related to the presence of iodides ensures enhanced catalyst stability. The benefits are most apparent under challenging conditions, such as very low reaction concentrations, protic solvents or with the occurrence of impurities.
含碘的硝基-Grela型催化剂已被合成并应用于关环复分解(RCM)和交叉复分解(CM)反应。这些新型催化剂在空间位阻较小的烯烃转化反应中表现出更高的效率。与碘化物的存在相关的钌附近额外的空间位阻确保了催化剂稳定性的增强。在具有挑战性的条件下,如极低的反应浓度、质子溶剂或存在杂质时,这些优势最为明显。