ol6b01891_si_001.pdf (2.47 MB)

Alkynyl Acylammoniums as Electrophilic 3C Synthons in a Formal [3 + 3] Annulation: Access to Functionalized 4H‑Pyran-4-ones

Download (2.47 MB)
journal contribution
posted on 23.07.2016, 01:29 by Shuding Dong, Chao Fang, Weifang Tang, Tao Lu, Ding Du
Alkynyl acylammoniums generated in situ from alkynyl acids are first used as electrophilic 3C synthons in a formal [3 + 3] annulation with 1,3-dicarbonyl compounds for regioselective synthesis of functionalized 4H-pyran-4-ones via a 4-(dimethylamino)­pyridine/Lewis acid dual-activation strategy. This protocol paves the way for further investigation of alkynyl acylammoniums as 3C synthons for construction of diverse heterocyclic skeletons.

History

Exports