Kaithal Akash, Hölscher Markus, Leitner Walter
Max Planck Institute for Chemical Energy Conversion Stiftstraße 34-36 Mülheim a.d. Ruhr 45470 Germany
Institut für Technische und Makromolekulare Chemie, RWTH Aachen University Worringer Weg 2 52074 Aachen Germany.
Chem Sci. 2020 Nov 20;12(3):976-982. doi: 10.1039/d0sc05404f.
A catalytic reaction using syngas (CO/H) as feedstock for the selective β-methylation of alcohols was developed whereby carbon monoxide acts as a C1 source and hydrogen gas as a reducing agent. The overall transformation occurs through an intricate network of metal-catalyzed and base-mediated reactions. The molecular complex [Mn(CO)Br[HN(CHP Pr)]] comprising earth-abundant manganese acts as the metal component in the catalytic system enabling the generation of formaldehyde from syngas in a synthetically useful reaction. This new syngas conversion opens pathways to install methyl branches at sp carbon centers utilizing renewable feedstocks and energy for the synthesis of biologically active compounds, fine chemicals, and advanced biofuels.
开发了一种以合成气(CO/H)为原料用于醇选择性β-甲基化的催化反应,其中一氧化碳作为C1源,氢气作为还原剂。整个转化过程通过金属催化和碱介导反应的复杂网络进行。由储量丰富的锰构成的分子络合物[Mn(CO)Br[HN(CHP Pr)]]作为催化体系中的金属组分,能在一个具有合成实用性的反应中从合成气生成甲醛。这种新的合成气转化开辟了利用可再生原料和能源在sp碳中心安装甲基支链的途径,用于合成生物活性化合物、精细化学品和先进生物燃料。