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An Asymmetric Diels–Alder Reaction Catalyzed by Chiral Phosphate Magnesium Complexes: Highly Enantioselective Synthesis of Chiral Spirooxindoles
Author(s) -
Li Guilong,
Liang Tao,
Wojtas Lukasz,
Antilla Jon C.
Publication year - 2013
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201209295
Subject(s) - enantioselective synthesis , diels–alder reaction , catalysis , magnesium phosphate , magnesium , chemistry , organic chemistry , phosphate , combinatorial chemistry
Mild Magic : A mild, enantioselective Diels–Alder reaction, catalyzed by a chiral magnesium phosphate species, has been developed for the synthesis of various chiral spirooxindoles. Molecular sieves were found to have a considerable effect when used as additives in this reaction.
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