Home / Publications / Synthesis of monoterpenic α-amino ketones

Synthesis of monoterpenic α-amino ketones

Pavel Anatol'evich Petukhov 1
Pavel Anatol'evich Petukhov
, 
Alexey Vasil'evich Tkachev 2
Alexey Vasil'evich Tkachev
10.1070/MC1996v006n02ABEH000582
Published 1996-04-30
Communication , Volume 6, Issue 2, 64-66
4
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Petukhov P. A., Tkachev A. V. Synthesis of monoterpenic α-amino ketones // Mendeleev Communications. 1996. Vol. 6. No. 2. pp. 64-66.
GOST all authors (up to 50) Copy
Petukhov P. A., Tkachev A. V. Synthesis of monoterpenic α-amino ketones // Mendeleev Communications. 1996. Vol. 6. No. 2. pp. 64-66.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1070/MC1996v006n02ABEH000582
UR - https://mendcomm.colab.ws/publications/10.1070/MC1996v006n02ABEH000582
TI - Synthesis of monoterpenic α-amino ketones
T2 - Mendeleev Communications
AU - Petukhov, Pavel Anatol'evich
AU - Tkachev, Alexey Vasil'evich
PY - 1996
DA - 1996/04/30
PB - Mendeleev Communications
SP - 64-66
IS - 2
VL - 6
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{1996_Petukhov,
author = {Pavel Anatol'evich Petukhov and Alexey Vasil'evich Tkachev},
title = {Synthesis of monoterpenic α-amino ketones},
journal = {Mendeleev Communications},
year = {1996},
volume = {6},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1996v006n02ABEH000582},
number = {2},
pages = {64--66},
doi = {10.1070/MC1996v006n02ABEH000582}
}
MLA
Cite this
MLA Copy
Petukhov, Pavel Anatol'evich, and Alexey Vasil'evich Tkachev. “Synthesis of monoterpenic α-amino ketones.” Mendeleev Communications, vol. 6, no. 2, Apr. 1996, pp. 64-66. https://mendcomm.colab.ws/publications/10.1070/MC1996v006n02ABEH000582.

Abstract

Terpenic α-amino ketones have been prepared in good yield by treatment of the corresponding α-amino oximes with Ti(III) salts; all other known methods of deoximation give unacceptably low yields.

References

1.
10.1070/MC1996v006n02ABEH000582_bib1
Atta-ur-Rahman
Stereoselective Synthesis in Organic Chemistry, 1993
2.
Synthesis and Cytotoxic Evaluation of Some Cyclic Arylidene Ketones and Related Oximes, Oxime Esters, and Analogs
Dimmock J.R., Sidhu K.K., Chen M., Li J., Quail J.W., Allen T.M., Kao G.Y.
Journal of Pharmaceutical Sciences, 1994
3.
10.1070/MC1996v006n02ABEH000582_bib3
Vasileva
Dokl. Bulg. Akad. Nauk., 1991
5.
Stereochemistry of α-Amino Oximes From the Monoterpene Hydrocarbons Car-3-ene, Limonene and α-Pinene
Tkachev A., Rukavishnikov A., Chibiryaev A., Denisov A., Gatilov Y., Bagryanskaya I.
Australian Journal of Chemistry, 1992
8.
Optically active ZnII and PtII complexes of the 3-carene type α-amino oxime
Tkachev A.V., Petukhov P.A., Konchenko S.N., Korenev S.V., Fedotov M.A., Gatilov Y.V., Rybalova T.V., Kholdeeva O.A.
Tetrahedron Asymmetry, 1995
9.
Conversion of Terpenic Compounds to ω-Ketonitriles
Tkaohev A.V., Rukavishnikov A.V., Chibirjaev A.M., Volodarsky L.B.
Synthetic Communications, 1990
10.
10.1070/MC1996v006n02ABEH000582_bib10
Rukavishnikov
Zh. Org. Khim., 1989
13.
10.1070/MC1996v006n02ABEH000582_bib13_1
Widmark
Arkiv Kemi., 1957
14.
10.1070/MC1996v006n02ABEH000582_bib13_2
Tkachev
Zh. Org. Khim., 1990
15.
Irradiation of eucarvone in polar media
Hart H., Takino T.
Journal of the American Chemical Society, 1971
16.
H. Tse-Lok and Zia Ud Din, Synth. Commun., 1980, 10, 921; US Patent 4,296,038 Cl. 260 343.21; C07D311/93.