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Russian Chemical Reviews, 1997, Volume 66, Issue 1, Pages 43–52
DOI: https://doi.org/10.1070/RC1997v066n01ABEH000309
(Mi rcr1331)
 

This article is cited in 3 scientific papers (total in 3 papers)

Acylation of acetals and related geminal systems. The use of this reaction in the synthesis of phospholipids

E. E. Nifantyev, D. A. Predvoditelev

Department of Chemistry, Moscow State Pedagogical University,
Abstract: The practical significance of acylation of acetals, orthoesters, and their aza-analogues (oxazolines) in fine organic synthesis is considered. Attention is mainly focused on the application of this reaction to the design of glycerophosphatides and other types of phospholipids. The use of acylation of these geminal alkoxides and oxazolines makes it possible to optimise the strategy of the synthesis of polyfunctional ester systems. The bibliography includes 76 references.
Received: 16.10.1996
Bibliographic databases:
Document Type: Article
UDC: 547.953+547.915
Language: English
Original paper language: Russian


Citation: E. E. Nifantyev, D. A. Predvoditelev, “Acylation of acetals and related geminal systems. The use of this reaction in the synthesis of phospholipids”, Usp. Khim., 66:1 (1997), 47–56; Russian Chem. Reviews, 66:1 (1997), 43–52
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  • https://www.mathnet.ru/eng/rcr/v66/i1/p47
  • This publication is cited in the following 3 articles:
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