Daugulis Olafs, Roane James, Tran Ly Dieu
Department of Chemistry, University of Houston, Houston, Texas 77204-5003, United States.
Acc Chem Res. 2015 Apr 21;48(4):1053-64. doi: 10.1021/ar5004626. Epub 2015 Mar 10.
In recent years, carbon-hydrogen bond functionalization has evolved from an organometallic curiosity to a tool used in mainstream applications in the synthesis of complex natural products and drugs. The use of C-H bonds as a transformable functional group is advantageous because these bonds are the most abundant functionality in organic molecules. One-step conversion of these bonds to the desired functionality shortens synthetic pathways, saving reagents, solvents, and labor. Less chemical waste is generated as well, showing that this chemistry is environmentally beneficial. This Account describes the development and use of bidentate, monoanionic auxiliaries for transition-metal-catalyzed C-H bond functionalization reactions. The chemistry was initially developed to overcome the limitations with palladium-catalyzed C-H bond functionalization assisted by monodentate directing groups. By the use of electron-rich bidentate directing groups, functionalization of unactivated sp(3) C-H bonds under palladium catalysis has been developed. Furthermore, a number of abundant base-metal complexes catalyze functionalization of sp(2) C-H bonds. At this point, aminoquinoline, picolinic acid, and related compounds are among the most used and versatile directing moieties in C-H bond functionalization chemistry. These groups facilitate catalytic functionalization of sp(2) and sp(3) C-H bonds by iron, cobalt, nickel, copper, ruthenium, rhodium, and palladium complexes. Exceptionally general reactivity is observed, enabling, among other transformations, direct arylation, alkylation, fluorination, sulfenylation, amination, etherification, carbonylation, and alkenylation of carbon-hydrogen bonds. The versatility of these auxilaries can be attributed to the following factors. First, they are capable of stabilizing high oxidation states of transition metals, thereby facilitating the C-H bond functionalization step. Second, the directing groups can be removed, enabling their use in synthesis and functionalization of natural products and medicinally relevant substances. While the development of these directing groups presents a significant advance, several limitations of this methodology are apparent. The use of expensive second-row transition metal catalysts is still required for efficient sp(3) C-H bond functionalization. Furthermore, the need to install and subsequently remove the relatively expensive directing group is a disadvantage.
近年来,碳氢键官能团化已从一种有机金属领域的新奇事物发展成为合成复杂天然产物和药物的主流应用中所使用的一种工具。将碳氢键用作可转化官能团具有诸多优势,因为这些键是有机分子中最为丰富的官能团。将这些键一步转化为所需的官能团可缩短合成路线,节省试剂、溶剂和人力。同时产生的化学废物也更少,这表明这种化学方法对环境有益。本综述介绍了用于过渡金属催化的碳氢键官能团化反应的双齿单阴离子助剂的开发与应用。该化学方法最初是为克服由单齿导向基团辅助的钯催化碳氢键官能团化的局限性而开发的。通过使用富电子双齿导向基团,已实现了钯催化下未活化的sp(3)碳氢键官能团化。此外,许多常见的贱金属配合物可催化sp(2)碳氢键的官能团化反应。此时,氨基喹啉、吡啶甲酸及相关化合物属于碳氢键官能团化化学中最常用且用途广泛的导向基团。这些基团可促进铁、钴、镍、铜、钌、铑和钯配合物对sp(2)和sp(3)碳氢键进行催化官能团化。观察到其具有格外广泛的反应活性,除其他转化反应外,还能实现碳氢键的直接芳基化、烷基化、氟化、亚磺酰化、胺化、醚化、羰基化和烯基化反应。这些助剂用途广泛可归因于以下因素:其一,它们能够稳定过渡金属的高氧化态,从而促进碳氢键官能团化步骤;其二,导向基团可以去除,使其能够用于天然产物及与药物相关物质的合成和官能团化反应。尽管这些导向基团的开发取得了重大进展,但该方法的若干局限性也很明显。高效sp(3)碳氢键官能团化反应仍需要使用昂贵的第二周期过渡金属催化剂;此外,需要安装并随后除去相对昂贵的导向基团也是一个缺点。