Functionalization and Hydrogenation of Carbon Chains Derived from CO**

• DOI: 10.1002/anie.202202241
• Publication Date: 2022-02-28T10:16:30Z
• Authors: Maria Batuecas; Richard Y. Kong; Andrew J. P. White; Mark R. Crimmin
• Keywords: Chemistry, Multidisciplinary; Homologation; INSERTION; Metallocarbenes; MONOXIDE; Fischer-Tropsch; metallocarbene; OXIDATIVE ADDITION; COORDINATION; Multidisciplinary; Science & Technology; CARBENE; Organic Chemistry; 540; Communications; CO; Chemistry; HYDRIDE; MOLECULAR-HYDROGEN; Physical Sciences; Reaction Mechanisms; FISCHER-TROPSCH; COMPLEXES; Mechanism; DIHYDROGEN; 03 Chemical Sciences

AbstractSelective reactions that combine H2, CO and organic electrophiles (aldehyde, ketones, isocyanide) to form hydrogenated C3 and C4 carbon chains are reported. These reactions proceed by CO homologation mediated by [W(CO)6] and an aluminum(I) reductant, followed by functionalization and hydrogenation of the chain ends. A combination of kinetics (rates, KIEs) and DFT calculations has been used to gain insight into a key step which involves hydrogenation of a metallocarbene intermediate. These findings expand the extremely small scope of systems that combine H2 and CO to make well‐defined products with complete control over chain length and functionality.