Aziridine Ring Cleavage by Nucleophiles in Epimino Derivatives of 1,6-Anhydro-beta-D-hexopyranoses.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F02%3A00007086" target="_blank" >RIV/00216208:11310/02:00007086 - isvavai.cz</a>
Alternative codes found
RIV/61388963:_____/02:57020256
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Aziridine Ring Cleavage by Nucleophiles in Epimino Derivatives of 1,6-Anhydro-beta-D-hexopyranoses.
Original language description
The regioselectivity of aziridine ring cleavage by nucleophiles in a series of N-tosyl- and N-benzylepiminoderivatives of 1,6-anhydro-â-D-hexopyranoses of D-allo, D-manno and D-galacto configurations has been studied.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GA203%2F01%2F0862" target="_blank" >GA203/01/0862: The Effect of Configuration on Reactivity of Aziridine Derivatives of 1,6-Anhydro-beta-D-hexopyranoses</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2002
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
European Journal of Organic Chemistry
ISSN
1434-193X
e-ISSN
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Volume of the periodical
2002
Issue of the periodical within the volume
15
Country of publishing house
SR - SURINAME
Number of pages
11
Pages from-to
2449-2459
UT code for WoS article
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EID of the result in the Scopus database
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