[3+2]-Cycloaddition reaction of sydnones with alkynes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F18%3A39912455" target="_blank" >RIV/00216275:25310/18:39912455 - isvavai.cz</a>
Result on the web
<a href="https://www.beilstein-journals.org/bjoc/articles/14/113" target="_blank" >https://www.beilstein-journals.org/bjoc/articles/14/113</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3762/bjoc.14.113" target="_blank" >10.3762/bjoc.14.113</a>
Alternative languages
Result language
angličtina
Original language name
[3+2]-Cycloaddition reaction of sydnones with alkynes
Original language description
This review covers all known examples of [3 + 2]-cycloaddition between sydnones and both terminal as well as internal alkynes/cycloalkynes taken from literature since its discovery by Huisgen in 1962 up to the current date. Except enumeration of synthetic applications it also covers mechanistic studies, catalysis, effects of substituents and reaction conditions influencing reaction rate and regioselectivity.
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
10401 - Organic chemistry
Result continuities
Project
—
Continuities
S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Beilstein Journal of Organic Chemistry
ISSN
1860-5397
e-ISSN
—
Volume of the periodical
14
Issue of the periodical within the volume
June
Country of publishing house
DE - GERMANY
Number of pages
32
Pages from-to
1317-1348
UT code for WoS article
000434431600002
EID of the result in the Scopus database
2-s2.0-85048222141