Home / Publications / An Ene-type Reaction of Thionyl Chloride with Linear Isoprenoids

An Ene-type Reaction of Thionyl Chloride with Linear Isoprenoids

Vladimir Andreevich Dragan 1
Vladimir Andreevich Dragan
Aiexsander Makarovich Moiseenkov 1
Aiexsander Makarovich Moiseenkov
Published 1992-12-31
CommunicationVolume 2, Issue 4, 150-151
0
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Dragan V. A., Moiseenkov A. M. An Ene-type Reaction of Thionyl Chloride with Linear Isoprenoids // Mendeleev Communications. 1992. Vol. 2. No. 4. pp. 150-151.
GOST all authors (up to 50) Copy
Dragan V. A., Moiseenkov A. M. An Ene-type Reaction of Thionyl Chloride with Linear Isoprenoids // Mendeleev Communications. 1992. Vol. 2. No. 4. pp. 150-151.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1070/MC1992v002n04ABEH000179
UR - https://mendcomm.colab.ws/publications/10.1070/MC1992v002n04ABEH000179
TI - An Ene-type Reaction of Thionyl Chloride with Linear Isoprenoids
T2 - Mendeleev Communications
AU - Dragan, Vladimir Andreevich
AU - Moiseenkov, Aiexsander Makarovich
PY - 1992
DA - 1992/12/31
PB - Mendeleev Communications
SP - 150-151
IS - 4
VL - 2
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{1992_Dragan,
author = {Vladimir Andreevich Dragan and Aiexsander Makarovich Moiseenkov},
title = {An Ene-type Reaction of Thionyl Chloride with Linear Isoprenoids},
journal = {Mendeleev Communications},
year = {1992},
volume = {2},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1992v002n04ABEH000179},
number = {4},
pages = {150--151},
doi = {10.1070/MC1992v002n04ABEH000179}
}
MLA
Cite this
MLA Copy
Dragan, Vladimir Andreevich, and Aiexsander Makarovich Moiseenkov. “An Ene-type Reaction of Thionyl Chloride with Linear Isoprenoids.” Mendeleev Communications, vol. 2, no. 4, Dec. 1992, pp. 150-151. https://mendcomm.colab.ws/publications/10.1070/MC1992v002n04ABEH000179.

Abstract

A diethylaluminium chloride-catalysed ene-type reaction of thionyl chloride with citronellyl, geranyl and linalyl acetates, followed by treatment of the reaction mixture with methanol, leads smoothly to the corresponding allylic methyl sulfinates.

References

1.
10.1070/MC1992v002n04ABEH000179_bib1
Drabowicz
The Chemistry of Sulphones and Sulphoxides, 1988
2.
Regiospecific Ene Reaction of Benzenesulfinyl Chloride with Linear Isoprenoids
Moiseenkov A.M., Dragan V.A., Koptenkova V.A., Veselovsky V.V.
Synthesis, 1987
3.
10.1070/MC1992v002n04ABEH000179_bib2_2
Veselovsky
Izv. Akad. Nauk. SSSR, Ser. Khim., 1987