@article{e56b2f46c99646838b1126d3921060c9,
title = "Chiral strong Br{\o}nsted acid-catalyzed enantioselective addition reaction of simple olefins with ethyl glyoxylate",
abstract = "An enantioselective intermolecular carbonyl-ene reaction and a Friedel-Crafts-type reaction of 1,1,2-trisubstituted and 1,2-disubstituted simple olefins with ethyl glyoxylate were developed using F10BINOL-derived N-sulfonyl phosphoramide as the chiral strong Br{\o}nsted acid catalyst. The present reactions feature an atom-economical and environmentally benign approach to the synthesis of enantioenriched allylic and homoallylic alcohols.",
author = "Jun Kikuchi and Yuki Aizawa and Masahiro Terada",
note = "Funding Information: This work was partially supported by a Grant-in-Aid for Scientific Research on Innovative Areas “Hybrid Catalysis for Enabling Molecular Synthesis on Demand” from the MEXT, Japan (no. JP17H06447). Publisher Copyright: {\textcopyright} 2020 the Partner Organisations.",
year = "2020",
month = jun,
day = "7",
doi = "10.1039/d0qo00448k",
language = "English",
volume = "7",
pages = "1383--1387",
journal = "Organic Chemistry Frontiers",
issn = "2052-4110",
publisher = "Royal Society of Chemistry",
number = "11",
}