Synthesis of new bipyridine N,N,-dioxides and their application in asymmetric allylation of benzaldehyde and aldol addition to acetophenone
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F19%3A00518983" target="_blank" >RIV/68378271:_____/19:00518983 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11310/19:10393755
Result on the web
<a href="https://doi.org/10.1007/s00706-018-2289-5" target="_blank" >https://doi.org/10.1007/s00706-018-2289-5</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1007/s00706-018-2289-5" target="_blank" >10.1007/s00706-018-2289-5</a>
Alternative languages
Result language
angličtina
Original language name
Synthesis of new bipyridine N,N,-dioxides and their application in asymmetric allylation of benzaldehyde and aldol addition to acetophenone
Original language description
Chiral pyridine N-oxides and bipyridine N,N´-dioxides are an important class of heteroaromatic compounds with interesting chemical properties. Polarization of the N–O bond results in their electron-donation activity and makes them rather strong Lewis bases, which are able to activate Lewis acids such as trichlorosilanes. Therefore, they can catalyze a number of various reactions such as allylation and crotylation of aldehydes, aldol reactions, ring-opening of epoxides, and cyanosilylation of ketones and imides. Due to the general high interest in the development of new Lewis basic chiral organocatalysts, synthetic approaches providing new chiral compounds possessing the pyridine N-oxide moiety are desirable.n
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10302 - Condensed matter physics (including formerly solid state physics, supercond.)
Result continuities
Project
<a href="/en/project/GA17-07707S" target="_blank" >GA17-07707S: Development of New Syntheses of Azaheterocycles</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2019
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Monatshefte fur Chemie
ISSN
0026-9247
e-ISSN
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Volume of the periodical
150
Issue of the periodical within the volume
1
Country of publishing house
AT - AUSTRIA
Number of pages
20
Pages from-to
29-48
UT code for WoS article
000454953600005
EID of the result in the Scopus database
2-s2.0-85056640511