Dermenci Alpay, Coe Jotham W, Dong Guangbin
Pfizer Inc., Worldwide Medicinal Chemistry, Eastern Point Rd., Groton, CT 06340, USA.
Department of Chemistry and Biochemistry, University of Texas at Austin, 1 University Station A5300, Austin, TX 78712-0165, USA.
Org Chem Front. 2014 Jul 1;1(5):567-581. doi: 10.1039/c4qo00053f. Epub 2014 Mar 27.
New modes of chemical reactivity are of high value to synthetic organic chemistry. In this vein, carbon-carbon (C-C) activation is an emerging field that offers new possibilities for synthesizing valuable complex molecules. This review discusses the pioneering stoichiometric discoveries in this field up to the most recent synthetic applications that apply catalytic transformations. Specifically, the review focuses on C-C activation in relatively unstrained systems, including stoichiometric reactions, chelation-directed and chelation-free catalytic reactions. While the field of C-C activation of relatively unstrained systems is underdeveloped, we expect that this review will provide insight into new developments and pave the path for robust, practical applications.
化学反应的新模式对有机合成化学具有很高的价值。就此而言,碳-碳(C-C)活化是一个新兴领域,为合成有价值的复杂分子提供了新的可能性。本综述讨论了该领域从开创性的化学计量学发现到应用催化转化的最新合成应用。具体而言,本综述重点关注相对无张力体系中的C-C活化,包括化学计量反应、螯合导向和无螯合催化反应。虽然相对无张力体系的C-C活化领域尚不完善,但我们期望本综述能为新进展提供见解,并为强大的实际应用铺平道路。