Bailey Elliot P, Donohoe Timothy J, Smith Martin D
Chemistry Research Laboratory, University of Oxford, Oxford, UK.
Nat Commun. 2024 Jun 15;15(1):5131. doi: 10.1038/s41467-024-49249-2.
Hydrogen borrowing is an attractive and sustainable strategy for carbon-carbon bond formation that enables alcohols to be used as alkylating reagents in place of alkyl halides. However, despite intensive efforts, limited functional group tolerance is observed in this methodology, which we hypothesize is due to the high temperatures and harsh basic conditions often employed. Here we demonstrate that room temperature and functional group tolerant hydrogen borrowing can be achieved with a simple iridium catalyst in the presence of substoichiometric base without an excess of reagents. Achieving high yields necessitates the application of anaerobic conditions to counteract the oxygen sensitivity of the catalytic iridium hydride intermediate, which otherwise leads to catalyst degradation. Substrates containing heteroatoms capable of complexing the catalyst exhibit limited room temperature reactivity, but the application of moderately higher temperatures enables extension to a broad range of medicinally relevant nitrogen rich heterocycles. These newly developed conditions allow alcohols possessing functional groups that were previously incompatible with hydrogen borrowing reactions to be employed.
氢转移是一种用于碳-碳键形成的有吸引力且可持续的策略,它能使醇类替代卤代烃用作烷基化试剂。然而,尽管人们付出了巨大努力,但在这种方法中观察到的官能团耐受性有限,我们推测这是由于经常采用高温和苛刻的碱性条件所致。在此,我们证明了在亚化学计量碱存在且无过量试剂的情况下,使用一种简单的铱催化剂即可实现室温下的官能团耐受性氢转移。要实现高产率,必须采用厌氧条件以抵消催化氢化铱中间体对氧气的敏感性,否则会导致催化剂降解。含有能够与催化剂络合的杂原子的底物在室温下的反应性有限,但适度提高温度可将其应用扩展到广泛的与药物相关的富氮杂环化合物。这些新开发的条件允许使用以前与氢转移反应不相容的具有官能团的醇类。