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.
Document Type:
Article
Language: English
Citation:
P. A. Petukhov, A. V. Tkachev, “Synthesis of monoterpenic α-amino ketones”, Mendeleev Commun., 6:2 (1996), 64–66
Linking options:
https://www.mathnet.ru/eng/mendc4916
https://www.mathnet.ru/eng/mendc/v6/i2/p64
This publication is cited in the following 5 articles:
L. Bets, L. Vlad, F. Macaev, “The Reactions of (+)-2- and (+)-3-Carenes with the Retention of the Bicyclic Framework”, ChemJMold, 5:2 (2010), 6
A. M. Agafontsev, A. V. Tkachev, “Sulfuric acid-promoted rearrangement of 3-(N-acylamino)-substituted caran-4-one oximes”, Russ Chem Bull, 54:8 (2005), 1892
David H. Grayson, “Monoterpenoids”, Nat. Prod. Rep., 15:5 (1998), 439
V. D. Kolesnik, M. M. Shakirov, A. V. Tkachev, “Synthesis of diethyl oxo phosphonates from monoterpene ketones – carvone, pinocarvone and 2-caren-4-one”, Mendeleev Commun., 7:4 (1997), 141–143
P. A. PETUKHOV, A. V. TKACHEV, “ChemInform Abstract: Synthesis of Monoterpenic α‐Amino Ketones.”, ChemInform, 27:35 (1996)
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