Abstract:The C–H functionalization is a fundamentally important organic transformation to access C–C and C–heteroatom bonds in a common and/or complex molecular set-up during the preparation of small molecule bio-active scaffolds,...
“…bond-forming reactions were explored through noble as well as non-noble transition metal catalysis. 12 Amongst various C-C bond-forming processes, the direct C-H bond alkylation leading to alkylated arenes and heteroarenes represents a versatile reaction as the alkylated compounds are widely employed in pharmaceuticals, perfumery, and functional materials. Moreover, the intrinsic lipophilic nature of alkyl-unit imparts desired characteristics to drugs and agrochemicals.…”
Section: Chandini Pradhanmentioning
confidence: 99%
“…bond-forming reactions were explored through noble as well as non-noble transition metal catalysis. 12…”
Alkylation reaction stands as a crucial organic transformation, fostering privileged alkylated arenes and heteroarenes in molecular science. Over the past decade, utilization of the most abundant transition metal iron for...
“…bond-forming reactions were explored through noble as well as non-noble transition metal catalysis. 12 Amongst various C-C bond-forming processes, the direct C-H bond alkylation leading to alkylated arenes and heteroarenes represents a versatile reaction as the alkylated compounds are widely employed in pharmaceuticals, perfumery, and functional materials. Moreover, the intrinsic lipophilic nature of alkyl-unit imparts desired characteristics to drugs and agrochemicals.…”
Section: Chandini Pradhanmentioning
confidence: 99%
“…bond-forming reactions were explored through noble as well as non-noble transition metal catalysis. 12…”
Alkylation reaction stands as a crucial organic transformation, fostering privileged alkylated arenes and heteroarenes in molecular science. Over the past decade, utilization of the most abundant transition metal iron for...
“…3 As such, the selective C-H functionalization of alkanes is in high demand yet remains a formidable challenge for modern organic synthesis. The established strategies for selective C-H functionalization of alkanes are limited and fall into three categories: (i) metalcatalyzed C-H activation by actually inserting itself between carbon and hydrogen, [4][5][6] (ii) outer-sphere processes involving hydrogen atom transfer 7,8 or radical processes, [9][10][11][12][13] and (iii) metallocarbene C(sp 3 )-H insertion reactions. [14][15][16] Among these, C-H activation by metal-carbene-induced C-H insertion has received widespread attention and could achieve high siteand enantioselectivity without the need for a directing group or an external oxidant.…”
This review summarizes the developments in the C–H functionalization of saturated hydrocarbons (CnH2n+2 and CnH2n) through catalytic carbene insertion into their C–H bonds dated up to February 2024, based on the categories of the types of carbenes.
“…12 Nonetheless, in recent years, rare earth (RE) metal-based catalysts have also made advancements in multifunctional C–H functionalization reactions. 13 Cerium (Ce) is the most abundant element among rare earth metals. Industrially, cerium is primarily used in fluorescent materials and industrial exhaust gas treatment.…”
This review provides a comprehensive overview of metal catalysis in photo-electrochemical systems, discussing reaction mechanisms and offering prospects for this triadic catalytic mode.
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