Home / Articles / Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances

Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances

Vladimir Alexandrovich Glushkov 1
Vladimir Alexandrovich Glushkov
, 
Alexander Genrikhovich Tolstikov 1
Alexander Genrikhovich Tolstikov
1 Institute of technical Chemistry of Ural branch RAS, Perm
10.1070/RC2004v073n06ABEH000778
Published 30 November 2003
Communication , Volume 73, Issue 6, 581-608
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Glushkov V. A., Tolstikov A. G. Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances // Russian Chemical Reviews. 2004. Vol. 73. No. 6. pp. 581-608.
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Glushkov V. A., Tolstikov A. G. Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances // Russian Chemical Reviews. 2004. Vol. 73. No. 6. pp. 581-608.
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TY - JOUR
DO - 10.1070/RC2004v073n06ABEH000778
UR - https://rcr.colab.ws/publications/10.1070/RC2004v073n06ABEH000778
TI - Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances
T2 - Russian Chemical Reviews
AU - Glushkov, Vladimir Alexandrovich
AU - Tolstikov, Alexander Genrikhovich
PY - 2004
DA - 2003/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 581-608
IS - 6
VL - 73
ER -
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@article{2004_Glushkov,
author = {Vladimir Alexandrovich Glushkov and Alexander Genrikhovich Tolstikov},
title = {Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances},
journal = {Russian Chemical Reviews},
year = {2004},
volume = {73},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2004v073n06ABEH000778},
number = {6},
pages = {581--608},
doi = {10.1070/RC2004v073n06ABEH000778}
}
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Glushkov, Vladimir Alexandrovich, and Alexander Genrikhovich Tolstikov. “Chiral 1,3,2-oxazaborolidines in asymmetric synthesis: recent advances.” Russian Chemical Reviews, vol. 73, no. 6, Nov. 2004, pp. 581-608. https://rcr.colab.ws/publications/10.1070/RC2004v073n06ABEH000778.
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Abstract

The use of chiral 1,3,2-oxazaborolidines in asymmetric organic synthesis, particularly, in enantioselective reduction of ketones, imines and oxime ethers, asymmetric Diels–Alder reactions, aldol condensation and atroposelective reduction of lactones is reviewed. Reactions of immobilised 1,3,2-oxazaborolidines are also considered.

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