|
This article is cited in 19 scientific papers (total in 19 papers)
Asymmetric Michael addition of a glycine synthon to methyl methacrylate, mediated by disodium TADDOLate
Yu. N. Belokona, K. A. Kochetkova, T. D. Churkinaa, N. S. Ikonnikova, S. A. Orlovaa, V. V. Smirnovb, A. A. Chesnokovb a A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
b Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
Abstract:
The disodium salt of (4R,5R)-(TADDOL), 3, can be used as a mediator in the asymmetric Michael reaction, e.g. 1,4-addition of a glycine synthon 1 to methyl methacrylate 2, mediated by 3 (10–100 mol%), gives a diastereoisomeric excess of the corresponding product 4 up to 65% and an enantiomeric purity ca. 28%; (2S,4R)-4-methylglutamic acid (ee ≥ 85%), 6, was obtained starting from (2S,4R)-4 (ee 28%) through the recrystallization and decomposition of the latter.
Citation:
Yu. N. Belokon, K. A. Kochetkov, T. D. Churkina, N. S. Ikonnikov, S. A. Orlova, V. V. Smirnov, A. A. Chesnokov, “Asymmetric Michael addition of a glycine synthon to methyl methacrylate, mediated by disodium TADDOLate”, Mendeleev Commun., 7:4 (1997), 137–138
Linking options:
https://www.mathnet.ru/eng/mendc4823 https://www.mathnet.ru/eng/mendc/v7/i4/p137
|
|