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Levopimaric Acid Derived 1,2-Diamines and Their Application in the Copper-Catalyzed Asymmetric Henry Reaction Full article

Journal Tetrahedron
ISSN: 0040-4020 , E-ISSN: 1464-5416
Output data Year: 2018, Volume: 74, Number: 2, Pages: 260-267 Pages count : 8 DOI: 10.1016/j.tet.2017.11.059
Tags Asymmetric catalysis, Chiral pool, Diterpene, Enantioselectivity, Henry reaction, Levopimaric acid
Authors Khlebnikova Tatiana B. 1 , Konev Vasily N. 1 , Pai Zinaida P. 1
Affiliations
1 Boreskov Institute of Catalysis, Akad. Lavrentiev Pr. 5, Novosibirsk, 630090, Russian Federation

Funding (1)

1 Federal Agency for Scientific Organizations 0303-2016-0008

Abstract: Levopimaric acid, a readily available starting material, was used in efficient syntheses of new enantiopure diamines and Schiff bases with good yields. The synthetic procedure is based on the fumaropimaric acid monomethyl ester conversion into the optically pure trans-1,2-diamine via a Curtius rearrangement. New diamines were studied as ligands in the copper-catalyzed asymmetric Henry reaction.
Cite: Khlebnikova T.B. , Konev V.N. , Pai Z.P.
Levopimaric Acid Derived 1,2-Diamines and Their Application in the Copper-Catalyzed Asymmetric Henry Reaction
Tetrahedron. 2018. V.74. N2. P.260-267. DOI: 10.1016/j.tet.2017.11.059 WOS Scopus РИНЦ AN OpenAlex
Dates:
Submitted: Jun 20, 2017
Accepted: Nov 20, 2017
Published online: Nov 28, 2017
Published print: Jan 1, 2018
Identifiers:
Web of science: WOS:000423248700005
Scopus: 2-s2.0-85036631179
Elibrary: 35495899
Chemical Abstracts: 2017:1930344
OpenAlex: W2768625781
Citing:
DB Citing
Web of science 10
Scopus 10
Elibrary 13
OpenAlex 10
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