Simple and Fast Synthesis of New Axially Chiral Bipyridine N,N?-Dioxides for Highly Enantioselective Allylation of Aldehydes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F09%3A10000062" target="_blank" >RIV/00216208:11310/09:10000062 - isvavai.cz</a>
Alternative codes found
RIV/61388963:_____/09:00327368
Result on the web
—
DOI - Digital Object Identifier
—
Alternative languages
Result language
angličtina
Original language name
Simple and Fast Synthesis of New Axially Chiral Bipyridine N,N?-Dioxides for Highly Enantioselective Allylation of Aldehydes
Original language description
Unsymmetrically 3,3'-substituted axially chiral bis(tetrahydroisoquinoline) N,N'-dioxides exhibit unique catalytic activity in the asymmetric allylation of aromatic aldehydes (up to 96% ee). The product of the enantioselective allylation of benzaldehydeserved as abuilding block for the preparation of an intermediate in the synthesis of diospongine.
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CC - Organic chemistry
OECD FORD branch
—
Result continuities
Project
<a href="/en/project/LC06070" target="_blank" >LC06070: The structure and synthetic applications of transition metal complexes</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2009
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Advanced Synthesis & Catalysis
ISSN
1615-4150
e-ISSN
—
Volume of the periodical
351
Issue of the periodical within the volume
9
Country of publishing house
DE - GERMANY
Number of pages
5
Pages from-to
—
UT code for WoS article
000267894000014
EID of the result in the Scopus database
—