Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kouassi, Signo"'
Autor:
Evrard Ablo, Souleymane Coulibaly, Siomenan Coulibali, Kouassi Signo, Patrick‐Armand Achi, Nicolas Giraud, Gildas Bertho
Publikováno v:
Magnetic Resonance in Chemistry. 60:1157-1170
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9c107adbd23a6712f3385635b0da8ae
https://doi.org/10.1002/mrc.5308
https://doi.org/10.1002/mrc.5308
Autor:
Kouassi Signo, Sylvain Canesi
Publikováno v:
Organic Letters. 24:4939-4942
A synthesis of deoxyaspidodispermine was produced from homotyramine. This approach is based on the application of a functional protecting group strategy that not only masks the reactivity of sensitive groups during crucial steps but also possesses a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b715a3fcac4c88584b523271d8f3ebc2
https://doi.org/10.1021/acs.orglett.2c01878
https://doi.org/10.1021/acs.orglett.2c01878
Autor:
Evrard, Ablo, Souleymane, Coulibaly, Siomenan, Coulibali, Kouassi, Signo, Patrick-Armand, Achi, Nicolas, Giraud, Gildas, Bertho
Publikováno v:
Magnetic resonance in chemistry : MRCREFERENCES. 60(12)
Eighteen new N-acylhydrazones (9a-r) containing the imidazo[1,2-a]pyridine scaffold were synthesized through a seven steps reaction sequence, ending with a condensation of 2-(3-nitro-H-imidazo[1,2-a]pyridin-2-ylthio)acetohydrazide with various benzal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d3d8d663d4c2cec642551c8d6bd3187c
https://pubmed.ncbi.nlm.nih.gov/36057451
https://pubmed.ncbi.nlm.nih.gov/36057451
Autor:
null Ablo Evrard, null Souleymane Coulibaly, null Siomenan Coulibali, null Kouassi Signo, null Patrick‐Armand Achi, null Nicolas Giraud, null Gildas Bertho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5200cf770199e3754bd29357d1647b8c
https://doi.org/10.1002/mrc.5308/v3/response1
https://doi.org/10.1002/mrc.5308/v3/response1
Akademický článek
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Publikováno v:
The Journal of organic chemistry. 85(4)
In this study, the rapid transformation of inexpensive phenols into polyfunctionalized cyclohexenones containing a phosphonate in one pot is described. Such systems readily obtained from simple aromatic compounds could open up a multitude of syntheti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7888e5e4ffdd5cb186fc32faa5f59da
https://pubmed.ncbi.nlm.nih.gov/31939305
https://pubmed.ncbi.nlm.nih.gov/31939305
Publikováno v:
HETEROCYCLES. 103:1023
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee783b4fd35ad8be624dce1cf1d5cc97
https://doi.org/10.3987/com-20-s(k)44
https://doi.org/10.3987/com-20-s(k)44