Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anne Westermeyer"'
Autor:
Pierre-Georges Echeverria, Long-Sheng Zheng, Quentin Llopis, Bin He, Anne Westermeyer, Ricardo Molina Betancourt, Phannarath Phansavath, Virginie Ratovelomanana-Vidal
Publikováno v:
SynOpen, Vol 06, Iss 01, Pp 75-79 (2022)
Externí odkaz:
https://doaj.org/article/65b49bf78c43482e82be60110aa4520a
Autor:
Virginie Ratovelomanana-Vidal, Phannarath Phansavath, Pierre-Georges Echeverria, Long-Sheng Zheng, Quentin Llopis, Bin He, Anne Westermeyer, Ricardo Molina Betancourt
Publikováno v:
SynOpen. :75-79
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fae272188db6e2d27c0eabbbac224bd
https://doi.org/10.1055/s-0040-1719914
https://doi.org/10.1055/s-0040-1719914
Autor:
Anne Westermeyer, Phannarath Phansavath, Virginie Ratovelomanana-Vidal, Quentin Llopis, Gérard Guillamot
Publikováno v:
Synlett. 31:1172-1176
A regioselective synthesis of 3,5-disubstituted pyrazoles was achieved by 1,3-dipolar cycloaddition of diazo compounds, generated in situ from N-tosylhydrazones, with unactivated bromovinyl acetals, which served as alkyne surrogates. The reaction tol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4cec79f34a65168b30ea03b1f1d1bd9
https://doi.org/10.1055/s-0039-1690885
https://doi.org/10.1055/s-0039-1690885
Publikováno v:
New Journal of Chemistry. 44:20535-20543
The access to a new family of unusual 4-fluorinated pyrazoles bearing acetal moities at the 3- or 5-position has been achieved by electrophilic fluorination using Selectfluor® with yields up to 67%. The unconverted starting material can be recovered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f2b2cabd35464bddf04dc022bec07c7
https://doi.org/10.1039/d0nj05222a
https://doi.org/10.1039/d0nj05222a
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2020, 76, pp.131221-. ⟨10.1016/j.tet.2020.131221⟩
Tetrahedron, Elsevier, 2020, 76, pp.131221-. ⟨10.1016/j.tet.2020.131221⟩
The copper-catalyzed cycloisomerization of alkynylaziridines has been developed to access 2-substituted-4-formylpyrroles. The reaction proved to be tolerant to aryl and alkyl-substituted substrates which were readily prepared from the corresponding e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69a2762aa7a16921124707722f09bea7
https://hal.archives-ouvertes.fr/hal-03493777
https://hal.archives-ouvertes.fr/hal-03493777
Publikováno v:
Organic letters. 22(10)
The asymmetric reduction of β-keto-γ-acetal enamides has been investigated. A wide range of enantioenriched β-hydroxy-γ-acetal enamides were obtained through asymmetric transfer hydrogenation catalyzed by a tethered Rh(III)-DPEN complex with yiel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e68d3c5eed09c5f7c92e2750ae9fb2e0
https://pubmed.ncbi.nlm.nih.gov/32330052
https://pubmed.ncbi.nlm.nih.gov/32330052