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Usp. Khim., 2011, Volume 80, Issue 1, Pages 53–76 (Mi rcr38)  

This article is cited in 36 scientific papers (total in 36 papers)

Cyclopalladated complexes in enantioselective catalysis

V. V. Duninaa, O. N. Gorunovab, P. A. Zykova, K. A. Kochetkovb

a Lomonosov Moscow State University, Faculty of Chemistry
b A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, Moscow

Abstract: The results of the use of optically active palladacycles in enantioselective catalysis of [3,3]-sigmatropic rearrangements, aldol condensation, the Michael reaction and cross-coupling are analyzed. Reactions with allylic substrates or reagents and some other transformations are considered.

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Russian Chemical Reviews, 2011, 80:1, 51–74

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Document Type: Article
Received: 11.03.2010

Citation: V. V. Dunina, O. N. Gorunova, P. A. Zykov, K. A. Kochetkov, “Cyclopalladated complexes in enantioselective catalysis”, Usp. Khim., 80:1 (2011), 53–76; Russian Chem. Reviews, 80:1 (2011), 51–74

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    This publication is cited in the following articles:
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    2. Valery V. Dunina, Eugeniya I. Turubanova, Olga N. Gorunova, Michail V. Livantsov, Konstantin A. Lyssenko, Dmitrii Yu. Antonov, Yuri K. Grishin, “A planar chiral non-metallocenic analogue of the most popular N,N-dimethylbenzylaminate palladacycle”, Polyhedron, 2011  crossref  isi  scopus
    3. Dunina V.V., “Chiral Cyclopalladated Compounds: New Structures, Methodologies and Applications. a Personal Account”, Curr. Org. Chem., 15:18 (2011), 3415–3440  crossref  isi  elib  scopus
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    5. Adam Morel, Ewelina Silarska, Anna M. Trzeciak, Juliusz Pernak, “Palladium-catalyzed asymmetric Heck arylation of 2,3-dihydrofuran – effect of prolinate salts”, Dalton Trans, 42:4 (2013), 1215  crossref  isi  scopus
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    34. Konovalov A.I. Antipin I.S. Burilov V.A. Madzhidov T.I. Kurbangalieva A.R. Nemtarev A.V. Solovieva S.E. Stoikov I.I. Mamedov V.A. Zakharova L.Ya. Gavrilova E.L. Sinyashin O.G. Balova I.A. Vasilyev A.V. Zenkevich I.G. Krasavin M.Yu. Kuznetsov M.A. Molchanov A.P. Novikov M.S. Nikolaev V.A. Rodina L.L. Khlebnikov A.F. Beletskaya I.P. Vatsadze S.Z. Gromov S.P. Zyk N.V. Lebedev A.T. Lemenovskii D.A. Petrosyan V.S. Nenaidenko V.G. Negrebetskii V.V. Baukov Yu.I. Shmigol T.A. Korlyukov A.A. Tikhomirovg A.S. Shchekotikhing A.E. Traven V.F. Voskresenskii L.G. Zubkov F.I. Golubchikov O.A. Semeikin A.S. Berezin D.B. Stuzhin P.A. Filimonov V.D. Krasnokutskaya E.A. Fedorov A.Yu. Nyuchev A.V. Orlov V.Yu. Begunov R.S. Rusakov A.I. Kolobov A.V. Kofanov E.R. Fedotova O.V. Egorova A.Yu. Charushin V.N. Chupakhin O.N. Klimochkin Yu.N. Osyanin V.A. Reznikov A.N. Fisyuk A.S. Sagitullina G.P. Aksenov A.V. Aksenov N.A. Grachev M.K. Maslennikova V.I. Koroteev M.P. Brel A.K. Lisina S.V. Medvedeva S.M. Shikhaliev, “Modern Trends of Organic Chemistry in Russian Universities”, Russ. J. Organ. Chem., 54:2 (2018), 157–371  crossref  mathscinet  isi  scopus
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