Metal−Organic Cooperative Catalysis in C−H and C−C Bond Activation and Its Concurrent Recovery

• Published in: Accounts of chemical research Vol. 41; no. 2; pp. 222 - 234
• Main Authors: Park, Young Jun, Park, Jung-Woo, Jun, Chul-Ho
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 01.02.2008
• Subjects: Aldehydes - chemistry; Carbon - chemistry; Catalysis; Hydrogen - chemistry; Hydrogen Bonding; Metals - chemistry; Molecular Structure; Organic Chemicals - chemistry; Picolines - chemistry
• ISSN: 0001-4842; 1520-4898
• DOI: 10.1021/ar700133y

The development of an efficient catalytic activation (cleavage) system for C−H and C−C bonds is an important challenge in organic synthesis, because these bonds comprise a variety of organic molecules such as natural products, petroleum oils, and polymers on the earth. Among many elegant approaches utilizing transition metals to activate C−H and C−C bonds facilely, chelation-assisted protocols based on the coordinating ability of an organic moiety have attracted great attention, though they have often suffered from the need for an intact coordinating group in a substrate. In this Account, we describe our entire efforts to activate C−H or C−C bonds adjacent to carbonyl groups by employing a new concept of metal−organic cooperative catalysis (MOCC), which enables the temporal installation of a 2-aminopyridyl group into common aldehydes or ketones in a catalytic way. Consequently, a series of new catalytic reactions such as alcohol hydroacylation, oxo-ester synthesis, C−C triple bond cleavage, hydrative dimerization of alkynes, and skeletal rearrangements of cyclic ketones was realized through MOCC. In particular, in the quest for an optimized MOCC system composed of a Wilkinson’s catalyst (Ph3P)3RhCl and an organic catalyst (2-amino-3-picoline), surprising efficiency enhancements could be achieved when benzoic acid and aniline were introduced as promoters for the aldimine formation process. Furthermore, a notable accomplishment of C–C bond activation has been made using 2-amino-3-picoline as a temporary chelating auxiliary in the reactions of unstrained ketones with various terminal olefins and Wilkinson’s catalyst. In the case of seven-membered cyclic ketones, an interesting ring contraction to five- or six-membered ones takes place through skeletal rearrangements initiated by the C−C bond activation of MOCC. On the other hand, the fundamental advances of these catalytic systems into recyclable processes could be achieved by immobilizing both metal and organic components using a hydrogen-bonded self-assembled system as a catalyst support. This catalyst-recovery system provides a homogeneous phase at high temperature during the reaction and a heterogeneous phase at room temperature after the reaction. The product could be separated conveniently from the self-assembly support system by decanting the upper layer. The immobilized catalysts of both 2-aminopyridine and rhodium metal species sustained high catalytic activity for up to the eight catalytic reactions. In conclusion, the successful incorporation of an organocatalytic cycle into a transition metal catalyzed reaction led us to find MOCC for C−H and C−C bond activation. In addition, the hydrogen-bonded self-assembled support has been developed for an efficient and effective recovery system of homogeneous catalysts and could be successful in immobilizing both metal and organic catalysts.