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Russian Chemical Reviews, 1986, Volume 55, Issue 11, Pages 1026–1041
DOI: https://doi.org/10.1070/RC1986v055n11ABEH003238
(Mi rcr3756)
 

This article is cited in 16 scientific papers (total in 16 papers)

Alkyl Orthoesters and Their Applications in Organic Synthesis

L. A. Pavlova, Yu. A. Davidovich, S. V. Rogozhin

A. N. Nesmeyanov Institute of Organoelement Compounds, USSR Academy of Sciences, Moscow
Abstract: A systematic account is given of data characterising the chemical properties of alkyl esters of orthocarboxylic acids. The suggested reaction mechanisms are discussed and the extensive possibilities of the application of the orthoesters in the solution of various problems in organic synthesis are demonstrated.
The bibliography includes 91 references.
Bibliographic databases:
Document Type: Article
UDC: 547.303/306
Language: English
Original paper language: Russian


Citation: L. A. Pavlova, Yu. A. Davidovich, S. V. Rogozhin, “Alkyl Orthoesters and Their Applications in Organic Synthesis”, Usp. Khim., 55:11 (1986), 1803–1833; Russian Chem. Reviews, 55:11 (1986), 1026–1041
Linking options:
  • https://www.mathnet.ru/eng/rcr3756
  • https://doi.org/10.1070/RC1986v055n11ABEH003238
  • https://www.mathnet.ru/eng/rcr/v55/i11/p1803
  • This publication is cited in the following 16 articles:
    1. Alessia Petti, Kevin Lam, Sustainable and Functional Redox Chemistry, 2022, 29  crossref
    2. Balaneva N.N. Shestak O.P. Novikov V.L. Glazunov V.P., Russ. Chem. Bull., 70:8 (2021), 1584–1598  isi
    3. N. N. Balaneva, O. P. Shestak, V. L. Novikov, V. P. Glazunov, Russ Chem Bull, 70:8 (2021), 1584  crossref
    4. Anthony D. Garcia, Matthew C. Leech, Alessia Petti, Camille Denis, Iain C. A. Goodall, Adrian P. Dobbs, Kevin Lam, Org. Lett., 22:10 (2020), 4000  crossref
    5. Zahra Khademi, Kobra Nikoofar, RSC Adv., 10:51 (2020), 30314  crossref
    6. Julia S. Oshega, Boris V. Paponov, Irina V. Omelchenko, Oleg V. Shishkin, Mendeleev Communications, 25:2 (2015), 133  crossref
    7. Sarah Gibson, Dickie Romero, Hollie K. Jacobs, Aravamudan S. Gopalan, Tetrahedron Letters, 51:51 (2010), 6737  crossref
    8. Christopher J Fenk, Tetrahedron Letters, 40:45 (1999), 7955  crossref
    9. E. E. Nifantyev, D. A. Predvoditelev, Russian Chem. Reviews, 66:1 (1997), 43–52  mathnet  mathnet  crossref  isi  scopus
    10. Comprehensive Organic Functional Group Transformations, 1995, 735  crossref
    11. Glynn Mitchell, Comprehensive Organic Functional Group Transformations, 1995, 67  crossref
    12. Hidenori Okamoto, Shozo Kato, Bulletin of the Chemical Society of Japan, 64:3 (1991), 766  crossref
    13. Annual Reports in Organic Synthesis–1987, 1988, 427  crossref
    14. Vladimir F. Rudchenko, Sergei M. Ignatov, Ivan I. Chervin, Remir G. Kostyanovsky, Tetrahedron, 44:8 (1988), 2233  crossref
    15. L.I. Belen'Kii, Advances in Heterocyclic Chemistry, 44, Advances in Heterocyclic Chemistry Volume 44, 1988, 269  crossref
    16. L. A. PAVLOVA, YU. A. DAVIDOVICH, S. V. ROGOZHIN, ChemInform, 18:15 (1987)  crossref
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