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Plant coumarins: V. Palladium-catalyzed amination of 2-(1,3-dibromopropan-2-ylidene)oreoselone Full article

Journal Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393
Output data Year: 2010, Volume: 46, Number: 12, Pages: 1858-1868 Pages count : 11 DOI: 10.1134/S1070428010120158
Authors Lipeeva A.V. 1 , Shul'ts E.E. 1 , Shakirov M.M. 1 , Tolstikov G.A. 1
Affiliations
1 (Данные Web of science) Russian Acad Sci, Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Div, Novosibirsk 630090, Russia

Abstract: Palladium-catalyzed amination of 2-(1,3-dibromopropan-2-ylidene)-7H-furo[3,2-g]chromene-3,7(2H)-dione with various amines and amino acid derivatives led to the formation of the corresponding 2-(1,3-diaminopropan-2-ylidene)-substituted oreoselones. The yields depended on the catalytic system, base, and amine structure. Di- and polyazamacrocyclic furocoumarin derivatives were obtained by reactions of 2-(1,3-dibromopropan-2-ylidene)-7H-furo[3,2-g]chromene-3,7(2H)-dione with linear di- and polyamines (hexamethylenediamine, spermine, spermidine, and 3,6-dithiaoctane-1,8-diamine), catalyzed by palladium complexes.
Cite: Lipeeva A.V. , Shul'ts E.E. , Shakirov M.M. , Tolstikov G.A.
Plant coumarins: V. Palladium-catalyzed amination of 2-(1,3-dibromopropan-2-ylidene)oreoselone
Russian Journal of Organic Chemistry. 2010. V.46. N12. P.1858-1868. DOI: 10.1134/S1070428010120158 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Dec 1, 2010
Published online: Feb 5, 2011
Identifiers:
Web of science: WOS:000286985900015
Scopus: 2-s2.0-79951492840
Elibrary: 16699268
OpenAlex: W1987331809
Citing:
DB Citing
Web of science 7
Scopus 6
Elibrary 6
OpenAlex 4
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