Zobrazeno 1 - 10
of 42
pro vyhledávání: '"R. Ziyaev"'
Publikováno v:
Chemistry of Natural Compounds. 48:714-714
We previously isolated from leaves of Annona muricata L. (Annonaceae) and characterized the alkaloids anonaine, xylopine, isolaureline, and coclaurine. In continuation of the study of alkaloids from leaves of A. muricata collected in the Republic of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07c391cf10570919ac13e8334a695785
https://doi.org/10.1007/s10600-012-0363-5
https://doi.org/10.1007/s10600-012-0363-5
Publikováno v:
Chemistry of Natural Compounds. 35:366-367
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f69ce716430c04c31bc18dc91e4d890e
https://doi.org/10.1007/bf02234867
https://doi.org/10.1007/bf02234867
Publikováno v:
Chemistry of Natural Compounds. 27:516-517
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2951ca07fe5517c8e5a3392894d61565
https://doi.org/10.1007/bf00636592
https://doi.org/10.1007/bf00636592
Publikováno v:
Chemistry of Natural Compounds. 27:73-74
Cocculine, isoboldine, norisoboldine, and a new erythrinan alkaloid, coclafine, for which the structure and absolute configuration of 3S,5R-3,15-dihydroxyerythrin-Δ1(6)-ene have been established, have been isolated from the leaves ofCocculus laurifo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::978050c449ed940818c5ec2e5c12ce21
https://doi.org/10.1007/bf00629835
https://doi.org/10.1007/bf00629835
Publikováno v:
Chemistry of Natural Compounds. 31:276-276
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d831a788a1aa6a6ee150beb2876957de
https://doi.org/10.1007/bf01170231
https://doi.org/10.1007/bf01170231
Publikováno v:
Chemistry of Natural Compounds. 23:521-528
The alkaloids of the tulip treeLiriodendron tulipifera L., family Magnoliaceae, are considered. More then 20 alkaloids have been isolated during different vegetation periods from various organs of the plant growing in Uzbekistan, and these have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff1850ddae24ef0ac7abff7aa1af7f7f
https://doi.org/10.1007/bf00598665
https://doi.org/10.1007/bf00598665
Publikováno v:
Chemistry of Natural Compounds. 13:204-207
Six bases have been isolated from the leaves of the plantZiziphus jujuba Mill. family Rhamnaceae, cultivated in Tashkent: coclaurine, which has been isolated previously, and isoboldine, norisoboldine, asimilobine, which have been isolated for the fir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5946b801f13d63d560450e468500ab4
https://doi.org/10.1007/bf00563948
https://doi.org/10.1007/bf00563948
Publikováno v:
Chemistry of Natural Compounds. 11:495-497
As the result of a study of the leaves ofLiriodendron tulipifera L. according to the vegetation periods, it has been established that they contain the maximum amount of alkaloids in the spring and early vegetation period of the plant (0.32%) and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b7856be058669648a782385700dd759
https://doi.org/10.1007/bf00566793
https://doi.org/10.1007/bf00566793
Publikováno v:
Chemistry of Natural Compounds. 9:59-61
1. The leaves ofLiriodendron tulipifera have yielded a new alkaloid, lirinine. On the basis of a study of the UV, IR, NMR and mass spectra of lirinine the structure of 5-hydroxy-2,6-dimethoxyaporphine has been proposed for it.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e784ac0304733695745e92314de1de7
https://doi.org/10.1007/bf00580893
https://doi.org/10.1007/bf00580893
Publikováno v:
Chemistry of Natural Compounds. 9:727-729
From the leaves ofLiriodendron tulipifera have been isolated d-caaverine and a new aporphine alkaloid—lirinidine—with the composition C18H19O2N, [α]D25 +78° (c 0.19; chloroform).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::022753e7e8115f48202662af475c7452
https://doi.org/10.1007/bf00565796
https://doi.org/10.1007/bf00565796