Ali Wajid, Prakash Gaurav, Maiti Debabrata
Department of Chemistry, Indian Institute of Technology Bombay Powai Mumbai Maharashtra-400076 India
Tokyo Tech World Research Hub Initiative (WRHI), Laboratory for Chemistry and Life Science, Tokyo Institute of Technology Tokyo 152-8550 Japan.
Chem Sci. 2021 Jan 29;12(8):2735-2759. doi: 10.1039/d0sc05555g.
Transition metal-catalysed functionalizations of inert C-H bonds to construct C-C bonds represent an ideal route in the synthesis of valuable organic molecules. Fine tuning of directing groups, catalysts and ligands has played a crucial role in selective C-H bond (sp or sp) activation. Recent developments in these areas have assured a high level of regioselectivity in C-H olefination reactions. In this review, we have summarized the recent progress in the oxidative olefination of sp and sp C-H bonds with special emphasis on distal, atroposelective, non-directed sp and directed sp C-H olefination. The scope, limitation, and mechanism of various transition metal-catalysed olefination reactions have been described briefly.
过渡金属催化惰性C-H键官能团化以构建C-C键是合成有价值有机分子的理想途径。导向基团、催化剂和配体的精细调控在选择性C-H键(sp或sp)活化中发挥了关键作用。这些领域的最新进展确保了C-H烯基化反应具有高度的区域选择性。在本综述中,我们总结了sp和sp C-H键氧化烯基化的最新进展,特别强调了远程、阻转选择性、非导向sp和导向sp C-H烯基化。简要描述了各种过渡金属催化烯基化反应的范围、局限性和机理。