Synthesis of chiral 1,2-diamines from α-pinene and their use in asymmetric nitroaldol reaction

Verfasser / Beitragende:
[I. Dvornikova, E. Buravlev, K. Suponitskii, I. Chukicheva, A. Kutchin]
Ort, Verlag, Jahr:
2015
Enthalten in:
Russian Journal of Organic Chemistry, 51/4(2015-04-01), 480-492
Format:
Artikel (online)
ID: 605530254
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024 7 0 |a 10.1134/S1070428015040041  |2 doi 
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245 0 0 |a Synthesis of chiral 1,2-diamines from α-pinene and their use in asymmetric nitroaldol reaction  |h [Elektronische Daten]  |c [I. Dvornikova, E. Buravlev, K. Suponitskii, I. Chukicheva, A. Kutchin] 
520 3 |a Chiral diamines with C 1 and C 2 symmetry have been synthesized from 2-hydroxypinan-3-one and tested as ligands in Cu-catalyzed asymmetric nitroaldol reaction of nitromethane with 4-nitrobenzaldehyde. 
540 |a Pleiades Publishing, Ltd., 2015 
700 1 |a Dvornikova  |D I.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
700 1 |a Buravlev  |D E.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
700 1 |a Suponitskii  |D K.  |u Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, 119991, Moscow, Russia  |4 aut 
700 1 |a Chukicheva  |D I.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
700 1 |a Kutchin  |D A.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
773 0 |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/4(2015-04-01), 480-492  |x 1070-4280  |q 51:4<480  |1 2015  |2 51  |o 11178 
856 4 0 |u https://doi.org/10.1134/S1070428015040041  |q text/html  |z Onlinezugriff via DOI 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Dvornikova  |D I.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Buravlev  |D E.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Suponitskii  |D K.  |u Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, 119991, Moscow, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Chukicheva  |D I.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kutchin  |D A.  |u Institute of Chemistry, Komi Research Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, 167982, Syktyvkar, Russia  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Russian Journal of Organic Chemistry  |d Pleiades Publishing  |g 51/4(2015-04-01), 480-492  |x 1070-4280  |q 51:4<480  |1 2015  |2 51  |o 11178