@article{48d66b3f3cd04a519e06692cf6b2ca9e,
title = "Enantioselective hydrophosphinylation of 1-alkenylphosphine oxides catalyzed by chiral strong Br{\o}nsted base",
abstract = "A catalytic enantioselective addition of diarylphosphine oxides to 1-alkenyl(diaryl)phosphine oxides was achieved by using a chiral ureate as a chiral strong Br{\o}nsted base catalyst. The reaction followed by the reduction of phosphine oxide moieties provided chiral 1,2-diphosphinoalkanes, which are a family of useful chiral ligands for asymmetric transition metal catalysis.",
author = "Azusa Kondoh and Sho Ishikawa and Masahiro Terada",
note = "Funding Information: This research was supported by a Grant-in-Aid for Scientific Research on Innovative Areas “Hybrid Catalysis for Enabling Molecular Synthesis on Demand” (JP17H06447) from MEXT (Japan) and a Grant-in-Aid for Scientific Research (S) (JP16H06354) from the JSPS. We thank JSPS for a research fellowship for Young Scientists (S. I.). Publisher Copyright: {\textcopyright} The Royal Society of Chemistry.",
year = "2020",
month = oct,
day = "21",
doi = "10.1039/d0ob01778g",
language = "English",
volume = "18",
pages = "7814--7817",
journal = "Organic and Biomolecular Chemistry",
issn = "1477-0520",
publisher = "Royal Society of Chemistry",
number = "39",
}