Synthesis and rearrangement of Dewar benzenes into biaryls: Experimental evidence for conrotatory ring opening
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F08%3A12874" target="_blank" >RIV/00216208:11310/08:12874 - isvavai.cz</a>
Alternative codes found
RIV/61388963:_____/08:00310213 RIV/00216208:11310/08:12801
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Synthesis and rearrangement of Dewar benzenes into biaryls: Experimental evidence for conrotatory ring opening
Original language description
Rearrangement of aryl-substituted Dewar benzenes into the corresponding biaryls may serve as an alternative pathway for synthesis of sterically hindered biaryls. The kinetic data obtained from thermal rearrangements of Dewar benzenes provide experimental
Czech name
Synteza a preusporadani benzenu na biaryly.
Czech description
Synteza a preusporadani benzenu na biaryly.
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/1M0508" target="_blank" >1M0508: New Antivirals and Antineoplastics</a><br>
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2008
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
1
Issue of the periodical within the volume
1
Country of publishing house
DE - GERMANY
Number of pages
5
Pages from-to
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UT code for WoS article
000252681800003
EID of the result in the Scopus database
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