SYNTHESIS OF HYBRID MOLECULES CONTAINING FRAGMENTS OF SESQUITERPENE LACTONES AND PLANT ALKALOIDS Full article
Journal |
Chemistry of Natural Compounds
ISSN: 0009-3130 , E-ISSN: 1573-8388 |
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Output data | Year: 2011, Volume: 46, Number: 6, Pages: 880-885 Pages count : DOI: 10.1007/s10600-011-9774-y | ||||
Tags | isoalantolactone; 5'-iodolappaconitine; 6-bromodeoxyvasicinone; Pd acetate; cross-coupling reaction | ||||
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Abstract:
The Pd-catalyzed arylation of isoalantolactone by deoxyvasicinone and lappaconitine halides occurred with formation mainly of cross-coupling products with the (E)-configuration of the double bond. Another three compounds were isolated from the reaction of isoalantolactone with 6-bromodeoxyvasicinone. These were the lactone diarylation product, a compound with the (Z)-configuration of the double bond, and a product with a shift of the C(11,13) double bond and configuration inversion at C(8). The new compounds are interesting as potential biologically active agents.
Cite:
Belovodskii A.V.
, Shul'ts E.E.
, Shakirov M.M.
, Romanov V.E.
, Elmuradov B.Z.
, Shakhidoyatov K.M.
, Tolstikov G.A.
SYNTHESIS OF HYBRID MOLECULES CONTAINING FRAGMENTS OF SESQUITERPENE LACTONES AND PLANT ALKALOIDS
Chemistry of Natural Compounds. 2011. V.46. N6. P.880-885. DOI: 10.1007/s10600-011-9774-y WOS Scopus РИНЦ
SYNTHESIS OF HYBRID MOLECULES CONTAINING FRAGMENTS OF SESQUITERPENE LACTONES AND PLANT ALKALOIDS
Chemistry of Natural Compounds. 2011. V.46. N6. P.880-885. DOI: 10.1007/s10600-011-9774-y WOS Scopus РИНЦ
Dates:
Published print: | Jan 1, 2011 |
Published online: | Feb 8, 2011 |
Identifiers:
Web of science | WOS:000288438500011 |
Scopus | 2-s2.0-79952696502 |
Elibrary | 24939318 |
OpenAlex | W2009522262 |