| Literature DB >> 26864437 |
Lei Wang1, Sun Li1, Pankaj Chauhan1, Daniel Hack1, Arne R Philipps1, Rakesh Puttreddy2, Kari Rissanen2, Gerhard Raabe1, Dieter Enders3.
Abstract
A novel one-pot, three-component diastereo- and enantioselective synthesis of spiropyrazolones has been developed involving the aldol condensation of an enal to generate α,β-unsaturated pyrazolones, which react with a second equivalent of enal through an N-heterocyclic carbene (NHC)-catalyzed [3+2] annulation. The desired spirocyclopentane pyrazolones are obtained in moderate to good yields and good to excellent stereoselectivities. Alternatively, starting from cyclic 1,3-diketones, 2,5-chromenediones are available through [2+4] annulation.Entities:
Keywords: N-heterocyclic carbene; asymmetric synthesis; chromenedione; multicomponent reaction; spiropyrazolone
Year: 2016 PMID: 26864437 DOI: 10.1002/chem.201600515
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236