Alkynylation of heterocyclic compounds using hypervalent iodine reagent

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F15%3A10294429" target="_blank" >RIV/00216208:11310/15:10294429 - isvavai.cz</a>

Result on the web

<a href="http://dx.doi.org/10.1039/c4ob02625j" target="_blank" >http://dx.doi.org/10.1039/c4ob02625j</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c4ob02625j" target="_blank" >10.1039/c4ob02625j</a>

Result language

angličtina

Original language name

Alkynylation of heterocyclic compounds using hypervalent iodine reagent

Original language description

The alkynylation of various nitrogen- and/or sulphur-containing heterocyclic compounds using hypervalent iodine TMS-EBX by utilization of tertiary amines under mild conditions is described. The developed metal-free methodology furnishes the correspondingalkynylated heterocycles bearing quaternary carbon in high yields.

Czech name

—

Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

—

Project

<a href="/en/project/GAP207%2F10%2F0428" target="_blank" >GAP207/10/0428: Enantioselective organocatalytic alpha-alkynylation,alkenylation and arylation of aldehydes and ketones</a><br>

Continuities

S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year

2015

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Organic and Biomolecular Chemistry

ISSN

1477-0520

e-ISSN

—

Volume of the periodical

13

Issue of the periodical within the volume

10

Country of publishing house

GB - UNITED KINGDOM

Number of pages

6

Pages from-to

2884-2889

UT code for WoS article

000350674400007

EID of the result in the Scopus database

2-s2.0-84923862260