Pd-catalyzed allylic amination in supercritical carbon dioxide: Synthesis of carborane-containing terpenoids Full article
Journal |
Journal of Supercritical Fluids
ISSN: 1872-8162 , E-ISSN: 0896-8446 |
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Output data | Year: 2010, Volume: 54, Number: 2, Pages: 218-221 Pages count : 4 DOI: 10.1016/j.supflu.2010.04.010 | ||||
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Abstract:
Pd-catalyzed amination of allylic carbonates with N-(ortho-carboran-3-yl)-N-methylamine was carried out in supercritical CO2. It has been demonstrated that complete conversion of allylic carbonates to the corresponding carborane amines with excellent regioselectivity may be achieved in scCO2 (170 atm, 60 °C) using NaHCO3 as the acceptor base. The reaction offers a selective method for the preparation of allylic amines and provides a useful approach to new terpenoids.
Cite:
Lyubimov S.E.
, Kuchurov I.V.
, Verbitskaya T.A.
, Rastorguev E.A.
, Kalinin V.N.
, Zlotin S.G.
, Davankov V.A.
Pd-catalyzed allylic amination in supercritical carbon dioxide: Synthesis of carborane-containing terpenoids
Journal of Supercritical Fluids. 2010. V.54. N2. P.218-221. DOI: 10.1016/j.supflu.2010.04.010 Scopus OpenAlex
Pd-catalyzed allylic amination in supercritical carbon dioxide: Synthesis of carborane-containing terpenoids
Journal of Supercritical Fluids. 2010. V.54. N2. P.218-221. DOI: 10.1016/j.supflu.2010.04.010 Scopus OpenAlex
Identifiers:
Scopus: | 2-s2.0-77955304415 |
OpenAlex: | W2039152055 |