Structural studies of benzo[c]phenanthridine alkaloid free bases by NMR spectroscopy

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F00%3A00002490" target="_blank" >RIV/00216224:14310/00:00002490 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Structural studies of benzo[c]phenanthridine alkaloid free bases by NMR spectroscopy

Original language description

In the presence of OH- quaternary benzophenanthridine alkaloids (QBA) are converted into 6-hydroxyderivatives, which may change to bimolecular aminoacetals by elimination of H2O. Free bases of alkaloids chelerythrine, sanguilutine, sanguirubine, chelirubine, chelilutine, sanguinarine, nitidine and fagaronine were investigated. Pseudobases are found the only products of alkalization of the QBA in DMSO-d6 solutions using sodium carbonate.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

<a href="/en/project/VS96095" target="_blank" >VS96095: Laboratory of Structure and Dynamics of Biomolecules</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2000

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Chem. Listy

ISSN

0009-2770

e-ISSN

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Volume of the periodical

94

Issue of the periodical within the volume

11

Country of publishing house

CZ - CZECH REPUBLIC

Number of pages

2

Pages from-to

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UT code for WoS article

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EID of the result in the Scopus database

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