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Catalytic enantioselective Hosomi-Sakurai reaction of α-ketoesters promoted by chiral copper(ii) complexes.
Niwa, Yutaro; Miyake, Mayu; Hayakawa, Ichiro; Sakakura, Akira.
Affiliation
  • Niwa Y; Graduate School of Natural Science and Technology, Okayama University, 3-1-1, Tsushima-naka, Kita-ku, Okayama, Japan. sakakura@okayama-u.ac.jp.
  • Miyake M; Graduate School of Natural Science and Technology, Okayama University, 3-1-1, Tsushima-naka, Kita-ku, Okayama, Japan. sakakura@okayama-u.ac.jp.
  • Hayakawa I; Graduate School of Natural Science and Technology, Okayama University, 3-1-1, Tsushima-naka, Kita-ku, Okayama, Japan. sakakura@okayama-u.ac.jp.
  • Sakakura A; Graduate School of Natural Science and Technology, Okayama University, 3-1-1, Tsushima-naka, Kita-ku, Okayama, Japan. sakakura@okayama-u.ac.jp.
Chem Commun (Camb) ; 55(27): 3923-3926, 2019 Mar 28.
Article in En | MEDLINE | ID: mdl-30919859
ABSTRACT
A catalytic enantioselective Hosomi-Sakurai reaction of α-ketoesters has been developed. A copper(ii) complex with a chiral bis(oxazoline) ligand bearing methanesulfonamide groups shows excellent catalytic activity to give α,α-disubstituted α-hydroxyesters in high yields with high enantioselectivities. This is the first successful method for the catalytic enantioselective 1,2-addition of α-ketoesters with allylic silanes.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2019 Document type: Article Affiliation country: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2019 Document type: Article Affiliation country: Japón