| Literature DB >> 29360370 |
Ransheng Ding1, Christian Wolf1.
Abstract
Asymmetric thiourea and squaramide catalysis provides access to synthetically versatile α-oxetanyl and α-azetidinyl alkyl halides exhibiting a tetrasubstituted chiral carbon center with high yields and enantioselectivities. The products are readily transformed with negligible erosion of enantiopurity and excellent diastereoselectivity to a diverse group of multifunctional compounds including fluorooxindoles with two contiguous chirality centers, fluorinated heterocyclic spiranes, and polyspiro compounds.Entities:
Year: 2018 PMID: 29360370 PMCID: PMC5937693 DOI: 10.1021/acs.orglett.8b00039
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005