Аннотация:
Heterogeneous chiral Jørgensen–Hayashi catalyst promotes enantioselective Michael addition of malonates at cinnamic aldehydes. In combination with Ca(OTf)2, it provides high yields (up to 78%) and excellent enantiomeric excesses (up to 99%) of the adducts.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. A. Guryev, M. V. Anokhin, A. D. Averin, I. P. Beletskaya, “Heterogeneous Jørgensen–Hayashi catalyst for asymmetric Michael addition of malonates to α,β-enals. Cooperative effect with Ca(OTf)2”, Mendeleev Commun., 26:6 (2016), 469–470
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2248
https://www.mathnet.ru/rus/mendc/v26/i6/p469
Эта публикация цитируется в следующих 8 статьяx:
Baozhen Yang, Longkang Yang, Chengrong Lu, Bei Zhao, Yizhe Huang, “Enantioselective Michael addition of malonates to α,β-unsaturated ketones catalyzed by rare-earth metal amides RE[N(SiMe3)2]3 with phenoxy-functionalized amino alcohol proligands”, Tetrahedron Letters, 145 (2024), 155175
Valentine Ananikov, Vladimir Gevorgyan, Christina Moberg, Michinori Suginome, Anna Trzeciak, “Irina Beletskaya: Chemistry Excellence in Scientific Endeavors”, Organometallics, 42:18 (2023), 2415
Péter Bakó, Tamás Nemcsok, Zsolt Rapi, György Keglevich, “Enantioselective Michael Addition of Malonates to Enones”, COC, 24:7 (2020), 746
Sergey N. Adamovich, “New atranes and similar ionic complexes. Synthesis, structure, properties”, Applied Organom Chemis, 33:7 (2019)
J. Tůma, M. Kohout, “Silica gel-immobilized multidisciplinary materials applicable in stereoselective organocatalysis and HPLC separation”, RSC Adv., 8:3 (2018), 1174
A. I. Konovalov, I. S. Antipin, V. A. Burilov, T. I. Madzhidov, A. R. Kurbangalieva, A. V. Nemtarev, S. E. Solovieva, I. I. Stoikov, V. A. Mamedov, L. Ya. Zakharova, E. L. Gavrilova, O. G. Sinyashin, I. A. Balova, A. V. Vasilyev, I. G. Zenkevich, M. Yu. Krasavin, M. A. Kuznetsov, A. P. Molchanov, M. S. Novikov, V. A. Nikolaev, L. L. Rodina, A. F. Khlebnikov, I. P. Beletskaya, S. Z. Vatsadze, S. P. Gromov, N. V. Zyk, A. T. Lebedev, D. A. Lemenovskii, V. S. Petrosyan, V. G. Nenaidenko, V. V. Negrebetskii, Yu. I. Baukov, T. A. Shmigol', A. A. Korlyukov, A. S. Tikhomirov, A. E. Shchekotikhin, V. F. Traven', L. G. Voskresenskii, F. I. Zubkov, O. A. Golubchikov, A. S. Semeikin, D. B. Berezin, P. A. Stuzhin, V. D. Filimonov, E. A. Krasnokutskaya, A. Yu. Fedorov, A. V. Nyuchev, V. Yu. Orlov, R. S. Begunov, A. I. Rusakov, A. V. Kolobov, E. R. Kofanov, O. V. Fedotova, A. Yu. Egorova, V. N. Charushin, O. N. Chupakhin, Yu. N. Klimochkin, V. A. Osyanin, A. N. Reznikov, A. S. Fisyuk, G. , “Modern Trends of Organic Chemistry in Russian Universities”, Russ J Org Chem, 54:2 (2018), 157
Irina P. Beletskaya, Alexei D. Averin, “New trends in the cross-coupling and other catalytic reactions”, Pure and Applied Chemistry, 89:10 (2017), 1413
S. N. Adamovich, N. V. Vchislo, E. N. Oborina, I. A. Ushakov, I. B. Rozentsveig, “Novel α,β-unsaturated imine derivatives of 3-aminopropylsilatrane”, Mendeleev Commun., 27:5 (2017), 443–445