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A New Efficient Catalytic System for the Meyer-Schuster Rearrangement

Mark Beniaminovich Erman 1
Mark Beniaminovich Erman
Sergey E Gulyi 1
Sergey E Gulyi
Igor Sergeevich Aulchenko 1
Igor Sergeevich Aulchenko
1 Research Institute of Synthetic and Natural Fragrances, Moscow, Russian Federation
Published 1994-06-30
CommunicationVolume 4, Issue 3, 89-89
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Erman M. B., Gulyi S. E., Aulchenko I. S. A New Efficient Catalytic System for the Meyer-Schuster Rearrangement // Mendeleev Communications. 1994. Vol. 4. No. 3. pp. 89-89.
GOST all authors (up to 50) Copy
Erman M. B., Gulyi S. E., Aulchenko I. S. A New Efficient Catalytic System for the Meyer-Schuster Rearrangement // Mendeleev Communications. 1994. Vol. 4. No. 3. pp. 89-89.
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TY - JOUR
DO - 10.1070/MC1994v004n03ABEH000360
UR - https://mendcomm.colab.ws/publications/10.1070/MC1994v004n03ABEH000360
TI - A New Efficient Catalytic System for the Meyer-Schuster Rearrangement
T2 - Mendeleev Communications
AU - Erman, Mark Beniaminovich
AU - Gulyi, Sergey E
AU - Aulchenko, Igor Sergeevich
PY - 1994
DA - 1994/06/30
PB - Mendeleev Communications
SP - 89-89
IS - 3
VL - 4
ER -
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@article{1994_Erman,
author = {Mark Beniaminovich Erman and Sergey E Gulyi and Igor Sergeevich Aulchenko},
title = {A New Efficient Catalytic System for the Meyer-Schuster Rearrangement},
journal = {Mendeleev Communications},
year = {1994},
volume = {4},
publisher = {Mendeleev Communications},
month = {Jun},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1994v004n03ABEH000360},
number = {3},
pages = {89--89},
doi = {10.1070/MC1994v004n03ABEH000360}
}
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Erman, Mark Beniaminovich, et al. “A New Efficient Catalytic System for the Meyer-Schuster Rearrangement.” Mendeleev Communications, vol. 4, no. 3, Jun. 1994, pp. 89-89. https://mendcomm.colab.ws/publications/10.1070/MC1994v004n03ABEH000360.

Abstract

The Meyer-Schuster rearrangement is efficiently catalysed by a system comprising ammonium metavanadate, diphenyl silanediol and dicarboxylic acid.

References

1.
Use of oxo-metallic derivatives in isomerisation
Chabardes P., Kuntz E., Varagnat J.
Tetrahedron, 1977
3.
The rearrangement of tertiary propargyl alcohols to α,β-unsaturated aldehydes in the presence of polymeric organosilyl vanadates.
Erman M.B., Aul'chenko I.S., Kheifits L.A., Dulova V.G., Novikov J.N., Vol'pin M.E.
Tetrahedron Letters, 1976
4.
10.1070/MC1994v004n03ABEH000360_bib4
Erman
Papers of the IXth International Congress of Essential Oils, vol. 4, 1983
5.
See, for example, M. B. Erman, I. S. Aulchenko and L. A. Kheifits, Abstracts of the Vlth All-Union Conference Khimiya Atsetilena i ego Proizvodnykh (Chemistry of Acetylene and Its Derivatives), Baku: AzINEFTEKHIM, 1979, Part 2, p. 50 (in Russian).