New cyclization reaction affording dinitrogen heterocycles: extension and diastereoselectivity
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F03%3A00008232" target="_blank" >RIV/60461373:22310/03:00008232 - isvavai.cz</a>
Alternative codes found
RIV/60461373:22340/03:00008232
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
New cyclization reaction affording dinitrogen heterocycles: extension and diastereoselectivity
Original language description
The three-component cyclization has been extended to a series of diamines and oxo compounds affording products with high diastereoselectivity in particular cases. Some of the products were transformed to Deoxyvasicinone alkaloid analogues.
Czech name
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Czech description
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Classification
Type
D - Article in proceedings
CEP classification
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
<a href="/en/project/GA203%2F02%2F0306" target="_blank" >GA203/02/0306: New cyclization reaction affording dinitrogen heterocycles</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2003
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Article name in the collection
The Tenth Blue Danube Symposium on Heterocyclic Chemistry
ISBN
80-227-1938-2
ISSN
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e-ISSN
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Number of pages
1
Pages from-to
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Publisher name
Univerzita Slovenská technická univerzita (STU)
Place of publication
Bratislava
Event location
Vídeň
Event date
Sep 3, 2003
Type of event by nationality
EUR - Evropská akce
UT code for WoS article
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