Zobrazeno 1 - 10
of 167
pro vyhledávání: '"Yagamare, Fall"'
Publikováno v:
ACS Omega, Vol 5, Iss 40, Pp 26049-26055 (2020)
Externí odkaz:
https://doaj.org/article/90168e26dfb44894bbacc4876bbf6d1c
Publikováno v:
Results in Chemistry, Vol 4, Iss , Pp 100431- (2022)
A straightforward synthesis of 7-thia-(-)-muricatacin has been achieved from a commercially available starting material and using the furan approach, hence enlarging the scope of our methodology.
Externí odkaz:
https://doaj.org/article/d616987e7b554bf2a1b41372563dd588
Publikováno v:
Journal of Chemistry, Vol 2021 (2021)
A new vitamin D analogue with a trans-fused decalin as the CD-ring system and containing a sulphur atom in the side chain has been synthesized in our research group. The obtention of this analogue is based on a recently discovered transformation of h
Externí odkaz:
https://doaj.org/article/8f8f54404ce7483a82ac71dc61ba99d9
Autor:
Insa Seck, Ismaïla Ciss, Adama Diédhiou, Mamadou Baldé, Seydou Ka, Lalla A. Ba, Samba F. Ndoye, Bruno Figadère, Blandine Seon-Meniel, Generosa Gomez, Sandrine Cojean, Sébastien Pomel, Philippe M. Loiseau, Yagamare Fall, Matar Seck
Publikováno v:
Medicinal Chemistry Research. 32:158-164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4f5045491912302c4f56f26bb5e7324
https://doi.org/10.1007/s00044-022-02994-9
https://doi.org/10.1007/s00044-022-02994-9
Publikováno v:
Organic Chemistry Frontiers. 9:1522-1530
Synthesis of six novel Gemini cholesterol analogues and the binding mode of one of them to RORγ.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb19fb89a2770166deefb4d67f8fbf15
https://doi.org/10.1039/d2qo00040g
https://doi.org/10.1039/d2qo00040g
Autor:
Andrea Martínez, Hugo Santalla, Fátima Garrido, Aliou Hamady Barry, Mohamed Gaye, Yagamare Fall Diop
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 73, Iss 2, Pp 115-117 (2017)
The title compound, C21H36O3, contains an oxolane ring, and six defined stereocentres and may serve as a useful synthon for the synthesis of calcitriol analogues. The configurations of the chiral C atoms of the side chain were unambiguously establish
Externí odkaz:
https://doaj.org/article/fab4c413149349ea8bfdc5872a196dfc
Publikováno v:
Journal of Chemistry, Vol 2021 (2021)
A new vitamin D analogue with a trans-fused decalin as the CD-ring system and containing a sulphur atom in the side chain has been synthesized in our research group. The obtention of this analogue is based on a recently discovered transformation of h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::395edd4a00db0af5739c174f17790211
https://doi.org/10.1155/2021/6429427
https://doi.org/10.1155/2021/6429427
Publikováno v:
ARKIVOC, Vol 2015, Iss 7, Pp 195-215 (2015)
Externí odkaz:
https://doaj.org/article/2433dfa33df641f6bd85590786e913a7
Autor:
Uxía Gómez-Bouzó, Anna Y. Belorusova, Marcos L. Rivadulla, Hugo Santalla, Lieve Verlinden, Annemieke Verstuyf, Maria J Ferronato, Alejandro C. Curino, Maria M. Facchinetti, Yagamare Fall, Generosa Gómez, Natacha Rochel
Publikováno v:
Bioorganic Chemistry. 136:106528
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f29f8df93b9cea8f08fe1d59015f950
https://doi.org/10.1016/j.bioorg.2023.106528
https://doi.org/10.1016/j.bioorg.2023.106528
Publikováno v:
ACS Omega, Vol 5, Iss 40, Pp 26049-26055 (2020)
ACS Omega
ACS Omega
An unexpected ring expansion that converts hydrindanes into decalins via an unprecedented dyotropic reaction involving a mesylate group has been observed, and this paved the way for easy access to polyfunctionalized chiral decalins. These polyfunctio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fec9b7a9122f655266b63be4d94a5de
https://doaj.org/article/90168e26dfb44894bbacc4876bbf6d1c
https://doaj.org/article/90168e26dfb44894bbacc4876bbf6d1c