Eintrag weiter verarbeiten
An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one
Gespeichert in:
Zeitschriftentitel: | New Journal of Chemistry |
---|---|
Personen und Körperschaften: | , , , , , , , , , , , |
In: | New Journal of Chemistry, 39, 2015, 9, S. 6738-6741 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
Royal Society of Chemistry (RSC)
|
Schlagwörter: |
author_facet |
Zaiter, Jamila Achibat, Hanane Amiri, Ouafa Hafid, Abderrafia Khouili, Mostafa Rakib, El Mostapha Neves, Cláudia M. B. Neves, Maria Graça P. M. S. Silva, Artur M. S. Cavaleiro, José A. S. Almeida Paz, Filipe A. Faustino, Maria Amparo F. Zaiter, Jamila Achibat, Hanane Amiri, Ouafa Hafid, Abderrafia Khouili, Mostafa Rakib, El Mostapha Neves, Cláudia M. B. Neves, Maria Graça P. M. S. Silva, Artur M. S. Cavaleiro, José A. S. Almeida Paz, Filipe A. Faustino, Maria Amparo F. |
---|---|
author |
Zaiter, Jamila Achibat, Hanane Amiri, Ouafa Hafid, Abderrafia Khouili, Mostafa Rakib, El Mostapha Neves, Cláudia M. B. Neves, Maria Graça P. M. S. Silva, Artur M. S. Cavaleiro, José A. S. Almeida Paz, Filipe A. Faustino, Maria Amparo F. |
spellingShingle |
Zaiter, Jamila Achibat, Hanane Amiri, Ouafa Hafid, Abderrafia Khouili, Mostafa Rakib, El Mostapha Neves, Cláudia M. B. Neves, Maria Graça P. M. S. Silva, Artur M. S. Cavaleiro, José A. S. Almeida Paz, Filipe A. Faustino, Maria Amparo F. New Journal of Chemistry An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one Materials Chemistry General Chemistry Catalysis |
author_sort |
zaiter, jamila |
spelling |
Zaiter, Jamila Achibat, Hanane Amiri, Ouafa Hafid, Abderrafia Khouili, Mostafa Rakib, El Mostapha Neves, Cláudia M. B. Neves, Maria Graça P. M. S. Silva, Artur M. S. Cavaleiro, José A. S. Almeida Paz, Filipe A. Faustino, Maria Amparo F. 1144-0546 1369-9261 Royal Society of Chemistry (RSC) Materials Chemistry General Chemistry Catalysis http://dx.doi.org/10.1039/c5nj01306b <p>Pyrazole and pyrazolone moieties have shown important biological activities.</p> An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one New Journal of Chemistry |
doi_str_mv |
10.1039/c5nj01306b |
facet_avail |
Online |
finc_class_facet |
Chemie und Pharmazie |
format |
ElectronicArticle |
fullrecord |
blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAzOS9jNW5qMDEzMDZi |
id |
ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAzOS9jNW5qMDEzMDZi |
institution |
DE-L229 DE-D275 DE-Bn3 DE-Brt1 DE-D161 DE-Gla1 DE-Zi4 DE-15 DE-Rs1 DE-Pl11 DE-105 DE-14 DE-Ch1 |
imprint |
Royal Society of Chemistry (RSC), 2015 |
imprint_str_mv |
Royal Society of Chemistry (RSC), 2015 |
issn |
1144-0546 1369-9261 |
issn_str_mv |
1144-0546 1369-9261 |
language |
English |
mega_collection |
Royal Society of Chemistry (RSC) (CrossRef) |
match_str |
zaiter2015aneasysyntheticaccesstonewpyrazolespiroderivativesfrom3amino1phenyl2pyrazolin5one |
publishDateSort |
2015 |
publisher |
Royal Society of Chemistry (RSC) |
recordtype |
ai |
record_format |
ai |
series |
New Journal of Chemistry |
source_id |
49 |
title |
An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_unstemmed |
An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_full |
An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_fullStr |
An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_full_unstemmed |
An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_short |
An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_sort |
an easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
topic |
Materials Chemistry General Chemistry Catalysis |
url |
http://dx.doi.org/10.1039/c5nj01306b |
publishDate |
2015 |
physical |
6738-6741 |
description |
<p>Pyrazole and pyrazolone moieties have shown important biological activities.</p> |
container_issue |
9 |
container_start_page |
6738 |
container_title |
New Journal of Chemistry |
container_volume |
39 |
format_de105 |
Article, E-Article |
format_de14 |
Article, E-Article |
format_de15 |
Article, E-Article |
format_de520 |
Article, E-Article |
format_de540 |
Article, E-Article |
format_dech1 |
Article, E-Article |
format_ded117 |
Article, E-Article |
format_degla1 |
E-Article |
format_del152 |
Buch |
format_del189 |
Article, E-Article |
format_dezi4 |
Article |
format_dezwi2 |
Article, E-Article |
format_finc |
Article, E-Article |
format_nrw |
Article, E-Article |
_version_ |
1792333537110654980 |
geogr_code |
not assigned |
last_indexed |
2024-03-01T14:14:20.621Z |
geogr_code_person |
not assigned |
openURL |
url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=An+easy+synthetic+access+to+new+pyrazole+spiro+derivatives+from+3-amino-1-phenyl-2-pyrazolin-5-one&rft.date=2015-01-01&genre=article&issn=1369-9261&volume=39&issue=9&spage=6738&epage=6741&pages=6738-6741&jtitle=New+Journal+of+Chemistry&atitle=An+easy+synthetic+access+to+new+pyrazole+spiro+derivatives+from+3-amino-1-phenyl-2-pyrazolin-5-one&aulast=Faustino&aufirst=Maria+Amparo+F.&rft_id=info%3Adoi%2F10.1039%2Fc5nj01306b&rft.language%5B0%5D=eng |
SOLR | |
_version_ | 1792333537110654980 |
author | Zaiter, Jamila, Achibat, Hanane, Amiri, Ouafa, Hafid, Abderrafia, Khouili, Mostafa, Rakib, El Mostapha, Neves, Cláudia M. B., Neves, Maria Graça P. M. S., Silva, Artur M. S., Cavaleiro, José A. S., Almeida Paz, Filipe A., Faustino, Maria Amparo F. |
author_facet | Zaiter, Jamila, Achibat, Hanane, Amiri, Ouafa, Hafid, Abderrafia, Khouili, Mostafa, Rakib, El Mostapha, Neves, Cláudia M. B., Neves, Maria Graça P. M. S., Silva, Artur M. S., Cavaleiro, José A. S., Almeida Paz, Filipe A., Faustino, Maria Amparo F., Zaiter, Jamila, Achibat, Hanane, Amiri, Ouafa, Hafid, Abderrafia, Khouili, Mostafa, Rakib, El Mostapha, Neves, Cláudia M. B., Neves, Maria Graça P. M. S., Silva, Artur M. S., Cavaleiro, José A. S., Almeida Paz, Filipe A., Faustino, Maria Amparo F. |
author_sort | zaiter, jamila |
container_issue | 9 |
container_start_page | 6738 |
container_title | New Journal of Chemistry |
container_volume | 39 |
description | <p>Pyrazole and pyrazolone moieties have shown important biological activities.</p> |
doi_str_mv | 10.1039/c5nj01306b |
facet_avail | Online |
finc_class_facet | Chemie und Pharmazie |
format | ElectronicArticle |
format_de105 | Article, E-Article |
format_de14 | Article, E-Article |
format_de15 | Article, E-Article |
format_de520 | Article, E-Article |
format_de540 | Article, E-Article |
format_dech1 | Article, E-Article |
format_ded117 | Article, E-Article |
format_degla1 | E-Article |
format_del152 | Buch |
format_del189 | Article, E-Article |
format_dezi4 | Article |
format_dezwi2 | Article, E-Article |
format_finc | Article, E-Article |
format_nrw | Article, E-Article |
geogr_code | not assigned |
geogr_code_person | not assigned |
id | ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAzOS9jNW5qMDEzMDZi |
imprint | Royal Society of Chemistry (RSC), 2015 |
imprint_str_mv | Royal Society of Chemistry (RSC), 2015 |
institution | DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Rs1, DE-Pl11, DE-105, DE-14, DE-Ch1 |
issn | 1144-0546, 1369-9261 |
issn_str_mv | 1144-0546, 1369-9261 |
language | English |
last_indexed | 2024-03-01T14:14:20.621Z |
match_str | zaiter2015aneasysyntheticaccesstonewpyrazolespiroderivativesfrom3amino1phenyl2pyrazolin5one |
mega_collection | Royal Society of Chemistry (RSC) (CrossRef) |
physical | 6738-6741 |
publishDate | 2015 |
publishDateSort | 2015 |
publisher | Royal Society of Chemistry (RSC) |
record_format | ai |
recordtype | ai |
series | New Journal of Chemistry |
source_id | 49 |
spelling | Zaiter, Jamila Achibat, Hanane Amiri, Ouafa Hafid, Abderrafia Khouili, Mostafa Rakib, El Mostapha Neves, Cláudia M. B. Neves, Maria Graça P. M. S. Silva, Artur M. S. Cavaleiro, José A. S. Almeida Paz, Filipe A. Faustino, Maria Amparo F. 1144-0546 1369-9261 Royal Society of Chemistry (RSC) Materials Chemistry General Chemistry Catalysis http://dx.doi.org/10.1039/c5nj01306b <p>Pyrazole and pyrazolone moieties have shown important biological activities.</p> An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one New Journal of Chemistry |
spellingShingle | Zaiter, Jamila, Achibat, Hanane, Amiri, Ouafa, Hafid, Abderrafia, Khouili, Mostafa, Rakib, El Mostapha, Neves, Cláudia M. B., Neves, Maria Graça P. M. S., Silva, Artur M. S., Cavaleiro, José A. S., Almeida Paz, Filipe A., Faustino, Maria Amparo F., New Journal of Chemistry, An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one, Materials Chemistry, General Chemistry, Catalysis |
title | An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_full | An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_fullStr | An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_full_unstemmed | An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_short | An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_sort | an easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
title_unstemmed | An easy synthetic access to new pyrazole spiro derivatives from 3-amino-1-phenyl-2-pyrazolin-5-one |
topic | Materials Chemistry, General Chemistry, Catalysis |
url | http://dx.doi.org/10.1039/c5nj01306b |