249. Pd-Catalyzed [3+6+3+6] Macrocyclizations of Aryl α-Diazo-β-Ketoesters
     Zhuang Zhong, Adiran de Aguirre, Céline Besnard, Amalia I. Poblador-Bahamonde, Jérôme Lacour
     Adv. Synth. Catal. 2024, 366, 3029-3035

Thanks to Pd(II)-catalysis, an efficient synthesis of unsaturated macrocycles is achieved by [3+6+3+6] condensation of cyclic ethers with aryl a-diazo-b-ketoesters. The presence of the electron-rich aryl ester moieties forbids the use of dirhodium complexes as these diazo decomposition catalysts provoke unforeseen intermolecular C_sp2-H insertion reactions that derail the targeted reactivity. However, with Pd(acac)₂, using high concentration conditions (1 M), a variety of 18-membered macrocycles (16 examples) is afforded with both aryl and alkyl diazo reagents. Catalyst selection for either electrophilic aromatic substitution (Rh) or ylide (Pd) pathways are explained by computational approaches.

DOI : 10.1002/adsc.202400118 

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