| Literature DB >> 30393576 |
Andrew J Smaligo1, Sriramurthy Vardhineedi1, Ohyun Kwon1.
Abstract
We have prepared a previously unreported family of P-stereogenic [2.2.1] bicyclic chiral phosphines through straightforward syntheses starting from the natural product carvone. This design rationale prompted the development of an unforeseen C-dealkenylation reaction. We have applied these organocatalysts in the asymmetric syntheses of a bevy of pyrrolines, obtained in high yields and enantioselectivities, including a biologically active small molecule, efsevin.Entities:
Keywords: annulation; carvone; chiral pool; enantioselective; heterocycle; organocatalysis; phosphine
Year: 2018 PMID: 30393576 PMCID: PMC6208446 DOI: 10.1021/acscatal.8b01081
Source DB: PubMed Journal: ACS Catal Impact factor: 13.084