Aleksandra Błocka, Jakub Ostapko and Wojciech Chaładaj
Chem. Commun., 2023,59, 5547-5550
Abstract
Application of aryl triflates and terminal acetylenic enamines as surrogates of unactivated ketones enables an unprecedented Pd-catalyzed 5-exo-dig cyclization/cross coupling sequence.
Yi Chen, Jianing Wu, Yongzheng Ding and Hanmin Huang
Org. Chem. Front., 2025,12, 85-89
Abstract
Transition metal-catalyzed hydrocarbonylation of alkenes has been widely studied; however, the hydrocarbonylation reaction that took place between two alkenes has been largely unexplored.
Nitin L Jadhao, Harish B. Musale, Jayant M. Gajbhiye and Vivek T. Humne
Org. Biomol. Chem., 2024,22, 521-528
Abstract
The direct synthesis of 2-aminothiazole has been developed from oxime acetate using a copper catalyst. The applicability of the present method is used in the formal synthesis of fentiazac.
Tian-Shu Wu, Yong-Jiu Hao, Zhong-Jian Cai and Shun-Jun Ji
Org. Chem. Front., 2024,11, 1057-1061
Abstract
This work describes a ligand-controlled regioselective ring-opening/defluorinative annulation of gem-DFCPs with enaminones, which provides an alternative strategy for the divergent synthesis of pyrroles.
Bedadyuti Vedvyas Pati, Nitha Nahan Puthalath, Shyam Kumar Banjare, Tanmayee Nanda and Ponneri C. Ravikumar
Org. Biomol. Chem., 2023,21, 2842-2869
Abstract
The 1,3-diynes hold a prominent position among the many coupling partners employed in metal-catalysed C–H activation because of their ability to form complex bis-heterocycles in one shot.