A convenient route to 2-hydroxy- and 2,15-dihydroxyhexahelicene
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F07%3A00086550" target="_blank" >RIV/61388963:_____/07:00086550 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
A convenient route to 2-hydroxy- and 2,15-dihydroxyhexahelicene
Original language description
2-Hydroxy- and 2,15-dihydroxyhexahelicene were synthesized from simple benzene and naphthalene building blocks by intramolecular CoI- or Ni0-catalyzed [2+2+2] cycloisomerization of CH3O-substituted aromatic triynes.
Czech name
Pohodlná cesta k 2-hydroxy- a 2,15-dihydroxyhexahelicenu
Czech description
2-Hydroxy- a 2,15-dihydroxyhexahelicen byly syntetizovány z jednoduchých benzenových a naftalenových stavebních bloků pomocí intramolekulární [2+2+2] cykloizomerační reakce katalyzované komplexy kobaltu(I) a niklu(0).
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
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)<br>R - Projekt Ramcoveho programu EK
Others
Publication year
2007
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
-
Issue of the periodical within the volume
25
Country of publishing house
DE - GERMANY
Number of pages
7
Pages from-to
4244-4250
UT code for WoS article
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EID of the result in the Scopus database
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