Heck Reactions of 6- and 2-Halopurines

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F08%3A00020047" target="_blank" >RIV/60461373:22310/08:00020047 - isvavai.cz</a>

Result on the web

—

DOI - Digital Object Identifier

—

Result language

angličtina

Original language name

Heck Reactions of 6- and 2-Halopurines

Original language description

9-Benzyl-6-iodopurine affords under the conditions of the Heck reaction mainly the corresponding 6,6´-dimer. The Heck product is formed in low yield (<= 12%). With 7-benzyl-6-iodopurine the dimerization is suppressed and the Heck product is obtained in 32 - 91% yield. 9-Substituted 6-chloro-2-iodopurines react smoothly giving 2-alkenyl-6-chloropurines in 71 - 97 % isolated yield.

Czech name

Heckova reakce 6- a 2-halogenpurinů

Czech description

9-Benzyl-6-iodopuriny poskytuje za podmínek Heckovy reakce převážně odpovídající 6,6´-dimer.

Type

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

CEP classification

CC - Organic chemistry

OECD FORD branch

—

Project

Result was created during the realization of more than one project. More information in the Projects tab.

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2008

Confidentiality

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

Name of the periodical

European Journal of Organic Chemistry

ISSN

1434-193X

e-ISSN

—

Volume of the periodical

—

Issue of the periodical within the volume

17

Country of publishing house

DE - GERMANY

Number of pages

6

Pages from-to

—

UT code for WoS article

000257045000008

EID of the result in the Scopus database

—