Utilization of DmbNHNH2 in the synthesis of amino-substituted 4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)phenols

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F12%3A33141481" target="_blank" >RIV/61989592:15310/12:33141481 - isvavai.cz</a>

Alternative codes found

RIV/61389030:_____/12:00382518

Result on the web

<a href="http://dx.doi.org/10.1016/j.tet.2012.03.063" target="_blank" >http://dx.doi.org/10.1016/j.tet.2012.03.063</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.tet.2012.03.063" target="_blank" >10.1016/j.tet.2012.03.063</a>

Result language

angličtina

Original language name

Utilization of DmbNHNH2 in the synthesis of amino-substituted 4-((3,5-diamino-1H-pyrazol-4-yl)diazenyl)phenols

Original language description

(2,4-Dimethoxybenzyl)hydrazine (DmbNHNH2) was utilized in the synthesis of Dmb-protected 4-((3,5- diamino-1H-pyrazol-4-yl)diazenyl)phenols. This unambiguous protection of the pyrazole endocyclic nitrogen atom enabled the preparation of amino-substituted4-((3,5-diamino-1H-pyrazol-4yl)diazenyl) phenols that were inaccessible through direct substitution. The Boc group could be selectively cleaved in the presence of the Dmb group.

Czech name

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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

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Project

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Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach

Publication year

2012

Confidentiality

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

Name of the periodical

Tetrahedron

ISSN

0040-4020

e-ISSN

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Volume of the periodical

68

Issue of the periodical within the volume

21

Country of publishing house

GB - UNITED KINGDOM

Number of pages

7

Pages from-to

3996-4002

UT code for WoS article

000303846900012

EID of the result in the Scopus database

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