Institute of Chemical Research of Catalonia (ICIQ), Barcelona Institute of Science and Technology (BIST), Av. Països Catalans 16, 43007, Tarragona, Spain.
Departament de Química Orgànica i Analítica, Universitat Rovira i Virgili (URV), C/Marcel⋅lí Domingo s/n, 43007, Tarragona, Spain.
Chempluschem. 2021 Sep;86(9):1283-1296. doi: 10.1002/cplu.202100232.
Gold(I) catalysts are ideal for the activation of alkynes under very mild conditions. However, unlike allenes or alkenes, the triple bond of alkynes cannot be prochiral. In addition, the linear coordination displayed by gold(I) complexes places the chiral ligand far away from the substrate resulting in an inefficient transfer of chiral information. This poses a significant challenge for the achievement of high enantiocontrol in gold(I)-catalyzed reactions of alkynes. Although considerable progress on enantioselective gold(I)-catalyzed transformations has recently been achieved, the asymmetric activation of non-prochiral alkyne-containing small molecules still represents a great challenge. Herein we summarize recent advances in intra- and intermolecular enantioselective gold(I)-catalyzed reactions involving alkynes, discussing new chiral ligand designs that lie at the basis of these developments. We also focus on the mode of action of these catalysts, their possible limitations towards a next-generation of more efficient ligand designs. Finally, square planar chiral gold(III) complexes, which offer an alternative to chiral gold(I) complexes, are also discussed.
金(I)催化剂非常适合在非常温和的条件下激活炔烃。然而,与丙二烯或烯烃不同,炔烃的三键不能是前手性的。此外,金(I)配合物显示的线性配位将手性配体远离底物,导致手性信息的传递效率低下。这给实现炔烃的金(I)催化反应的高对映体控制带来了重大挑战。尽管最近在对映选择性金(I)催化转化方面取得了相当大的进展,但非前手性炔烃小分子的不对称激活仍然是一个巨大的挑战。本文总结了涉及炔烃的分子内和分子间对映选择性金(I)催化反应的最新进展,讨论了这些发展所依据的新型手性配体设计。我们还重点讨论了这些催化剂的作用模式,以及它们在下一代更高效配体设计方面可能存在的局限性。最后,还讨论了具有替代手性金(I)配合物的平面四方手性金(III)配合物。