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Russian Chemical Reviews, 2000, Volume 69, Issue 12, Pages 1001–1019
DOI: https://doi.org/10.1070/RC2000v069n12ABEH000614
(Mi rcr1554)
 

This article is cited in 40 scientific papers (total in 40 papers)

Tandem transformations initiated and determined by the Michael reaction

E. V. Gorobets, M. S. Miftakhov, F. A. Valeev

Institute of Organic Chemistry, Ufa Scientific Centre of RAS
Abstract: Data on tandem transformations initiated by the Michael reaction published over the last five years are analysed, systematised and generalised. The bibliography includes 86 references.
Received: 17.07.2000
Bibliographic databases:
Document Type: Article
UDC: 547.917
Language: English
Original paper language: Russian


Citation: E. V. Gorobets, M. S. Miftakhov, F. A. Valeev, “Tandem transformations initiated and determined by the Michael reaction”, Usp. Khim., 69:12 (2000), 1091–1110; Russian Chem. Reviews, 69:12 (2000), 1001–1019
Linking options:
  • https://www.mathnet.ru/eng/rcr1554
  • https://doi.org/10.1070/RC2000v069n12ABEH000614
  • https://www.mathnet.ru/eng/rcr/v69/i12/p1091
  • This publication is cited in the following 40 articles:
    1. Liliya Kh. Faizullina, Yuliya A. Khalilova, Farid A. Valeev, Valentin N. Pavlov, Aleksandr V. Samorodov, Chem Heterocycl Comp, 57:9 (2021), 966  crossref
    2. Efremova I.E., Serebryannikova A.V., Belyakov A.V., Lapshina L.V., Russ. J. Gen. Chem., 89:3 (2019), 536–539  crossref  isi  scopus
    3. Richard C. Larock, Anton V. Dubrovskiy, Nataliya A. Markina, Comprehensive Organic Transformations, 2018, 1  crossref
    4. Boerth J.A., Ellman J.A., Chem. Sci., 7:2 (2016), 1474–1479  crossref  isi  scopus
    5. Boerth J.A., Hummel J.R., Ellman J.A., Angew. Chem.-Int. Edit., 55:41 (2016), 12650–12654  crossref  isi  scopus
    6. Jeffrey A. Boerth, Joshua R. Hummel, Jonathan A. Ellman, Angewandte Chemie, 128:41 (2016), 12840  crossref
    7. Biktagirov I.M., Faizullina L.Kh., Salikhov Sh.M., Safarov M.G., Valeev F.A., Russ. J. Organ. Chem., 50:9 (2014), 1317–1322  crossref  isi  elib  scopus
    8. Dyachenko V.D., Karpov E.N., Russ. J. Gen. Chem., 83:7 (2013), 1394–1401  crossref  isi  elib  scopus
    9. Zyuzin I.N., Suponitsky K.Yu., Sheremetev A.B., J. Heterocycl. Chem., 49:3 (2012), 561–565  crossref  isi  elib  scopus
    10. Fustero S., Baez C., Sanchez-Rosello M., Asensio A., Miro J., del Pozo C., Synthesis, 44:12 (2012), 1863–1873  crossref  isi  elib  scopus
    11. Rulev A.Yu., Kotsuki H., Maddaluno J., Green Chem., 14:2 (2012), 503–508  crossref  isi  elib  scopus
    12. Martin Holan, Radek Pohl, Ivana Císařová, Ullrich Jahn, Eur J Org Chem, 2012:18 (2012), 3459  crossref
    13. Rulev A.Yu., Russ. Chem. Rev., 80:3 (2011), 197–218  mathnet  crossref  isi  elib  scopus
    14. Fuchun Xie, Hong Chen, Youhong Hu, Org. Lett., 12:13 (2010), 3086  crossref
    15. Sunil V. Pansare, Shubhangi V. Adsool, Rajendar Dyapa, Tetrahedron: Asymmetry, 21:7 (2010), 771  crossref
    16. Organic Mechanisms, 2010, 519  crossref
    17. Thomas Jerphagnon, M. Gabriella Pizzuti, Adriaan J. Minnaard, Ben L. Feringa, Chem. Soc. Rev., 38:4 (2009), 1039  crossref
    18. Galina P. Sagitullina, Anna K. Garkushenko, Evgeny G. Atavin, Reva S. Sagitullin, Mendeleev Communications, 19:3 (2009), 155  crossref
    19. Ali Samarat, Jihène Ben Kraïem, Taïcir Ben Ayed, Hassen Amri, Tetrahedron, 64:40 (2008), 9540  crossref
    20. Matthew L. Maddess, Miles N. Tackett, Steven V. Ley, 66, Natural Compounds as Drugs, 2008, 13  crossref
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