Parmar Diksha, Kumar Rohit, Sharma Upendra
C-H Activation & Phytochemistry Lab, Chemical Technology Division, CSIR-IHBT, Palampur 176061, India.
Org Biomol Chem. 2024 Jun 26;22(25):5032-5051. doi: 10.1039/d4ob00739e.
This review covers the journey of chiral amino acids as ligands in atroposelective C-H bond activation/functionalization transition metal catalysis. Herein, we intend to demonstrate how these chiral amino acids have evolved and flourished in this stimulating field. Unprotected amino acids, mono--protected amino acids, and di--protected amino acids have been devised for atroposelective C-H activation. In each section, we have briefly discuss the key successes of amino acids in the atroposelective synthesis of biaryls, heterobiaryls, and non-biaryl atropisomers and their advantages in atroposelective C-H activation.
本综述涵盖了手性氨基酸作为配体在对映选择性C-H键活化/官能团化过渡金属催化中的历程。在此,我们旨在展示这些手性氨基酸是如何在这个充满活力的领域中发展和繁荣的。已设计出未保护的氨基酸、单保护氨基酸和双保护氨基酸用于对映选择性C-H活化。在每一部分中,我们简要讨论了氨基酸在联芳基、杂联芳基和非联芳基阻转异构体的对映选择性合成中的关键成果及其在对映选择性C-H活化中的优势。