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

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

Eduard Evgen'evich Nifantyev 1
Eduard Evgen'evich Nifantyev
, 
Dmitrii Aleksandrovich Predvoditelev 1
Dmitrii Aleksandrovich Predvoditelev
1 Department of Chemistry, Moscow State Pedagogical University,
10.1070/RC1997v066n01ABEH000309
Published 30 November 1996
Communication , Volume 66, Issue 1, 43-52
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Nifantyev E. E., Predvoditelev D. A. Acylation of acetals and related geminal systems. The use of this reaction in the synthesis of phospholipids // Russian Chemical Reviews. 1997. Vol. 66. No. 1. pp. 43-52.
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Nifantyev E. E., Predvoditelev D. A. Acylation of acetals and related geminal systems. The use of this reaction in the synthesis of phospholipids // Russian Chemical Reviews. 1997. Vol. 66. No. 1. pp. 43-52.
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TY - JOUR
DO - 10.1070/RC1997v066n01ABEH000309
UR - https://rcr.colab.ws/publications/10.1070/RC1997v066n01ABEH000309
TI - Acylation of acetals and related geminal systems. The use of this reaction in the synthesis of phospholipids
T2 - Russian Chemical Reviews
AU - Nifantyev, Eduard Evgen'evich
AU - Predvoditelev, Dmitrii Aleksandrovich
PY - 1997
DA - 1996/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 43-52
IS - 1
VL - 66
ER -
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@article{1997_Nifantyev,
author = {Eduard Evgen'evich Nifantyev and Dmitrii Aleksandrovich Predvoditelev},
title = {Acylation of acetals and related geminal systems. The use of this reaction in the synthesis of phospholipids},
journal = {Russian Chemical Reviews},
year = {1997},
volume = {66},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC1997v066n01ABEH000309},
number = {1},
pages = {43--52},
doi = {10.1070/RC1997v066n01ABEH000309}
}
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Nifantyev, Eduard Evgen'evich, and Dmitrii Aleksandrovich Predvoditelev. “Acylation of acetals and related geminal systems. The use of this reaction in the synthesis of phospholipids.” Russian Chemical Reviews, vol. 66, no. 1, Nov. 1997, pp. 43-52. https://rcr.colab.ws/publications/10.1070/RC1997v066n01ABEH000309.
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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.

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