C-H Imidation of 7-Deazapurines

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F18%3A00491246" target="_blank" >RIV/61388963:_____/18:00491246 - isvavai.cz</a>

Alternative codes found

RIV/00216208:11310/18:10378027

Result on the web

<a href="https://pubs.acs.org/doi/10.1021/acsomega.8b00520" target="_blank" >https://pubs.acs.org/doi/10.1021/acsomega.8b00520</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1021/acsomega.8b00520" target="_blank" >10.1021/acsomega.8b00520</a>

Result language

angličtina

Original language name

C-H Imidation of 7-Deazapurines

Original language description

We developed and presented here a ferrocene-catalyzed C-H imidation of 7-deazapurines (pyrrolo[2,3-d]pyrimidines) with N-imidyl peroxyesters. The reactions occur regioselectively at position 8 in 7-deazapurines, leading to a series of 8-succinimido-, phtalimido-, or naphthalimido-7-deazapurine derivatives. Attempted hydrazinolysis of resulting 8-imidyl-7-deazapurines led to corresponding 8-amino-7-deazapurine, which was very unstable and quickly decomposed.

Czech name

—

Czech description

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Type

J_imp - Article in a specialist periodical, which is included in the Web of Science database

CEP classification

—

OECD FORD branch

10401 - Organic chemistry

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)

Publication year

2018

Confidentiality

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

Name of the periodical

ACS Omega

ISSN

2470-1343

e-ISSN

—

Volume of the periodical

3

Issue of the periodical within the volume

4

Country of publishing house

US - UNITED STATES

Number of pages

5

Pages from-to

4674-4678

UT code for WoS article

000434352800041

EID of the result in the Scopus database

2-s2.0-85046163470