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Chiral Bronsted Acid-Catalyzed Enantioselective Synthesis of Isoindolinone-Derived N(Acyl), S- Acetals (CROSBI ID 646738)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa

Suć, Josipa ; Dokli, Irena ; Gredičak, Matija Chiral Bronsted Acid-Catalyzed Enantioselective Synthesis of Isoindolinone-Derived N(Acyl), S- Acetals // 17th Tetrahedron Symposium (Book of Abstracts), Sitges (Barcelona), Spain, 28.6.-1.7.2016.. 2016

Podaci o odgovornosti

Suć, Josipa ; Dokli, Irena ; Gredičak, Matija

engleski

Chiral Bronsted Acid-Catalyzed Enantioselective Synthesis of Isoindolinone-Derived N(Acyl), S- Acetals

Organocatalytic asymmetric addition of thiols to N-acyl ketimines, which are generated in situ from 3-hydroxy isoindolinones, is described. The reaction proceeds smoothly with a broad range of ketimines and thiols using a chiral Brønsted acid catalyst to afford N(acyl), S-acetals comprising a tetrasubstituted stereocenter in high yields and enantioselectivities (up to 98.5:1.5 e.r.). The

Chiral Bronsted acid, asymmetric catalysis, thiol addition

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Podaci o prilogu

2016.

objavljeno

Podaci o matičnoj publikaciji

17th Tetrahedron Symposium (Book of Abstracts), Sitges (Barcelona), Spain, 28.6.-1.7.2016.

Podaci o skupu

17th tetrahedron Symposium

poster

28.06.2016-01.07.2016

Barcelona, Španjolska; Sitges, Španjolska

Povezanost rada

Kemija