Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Sarah Sulzer-Mossé"'
Autor:
Pierre Quinodoz, Amandine Kolleth, Dylan Dagoneau, Masahiko Yoshimura, Lucía Reyes Méndez, Mylène Joigneaux, Roman Staiger, Robin Horber, Sarah Sulzer‐Mossé, Aybike Bekar Cesaretli, Ulfet Karadeniz Yezer, Saron Catak, Alain De Mesmaeker
Publikováno v:
Helvetica Chimica Acta. 105
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::353b7abdef52c64b6a1b35a7a1e7aa69
https://doi.org/10.1002/hlca.202200093
https://doi.org/10.1002/hlca.202200093
Autor:
Zeynep Aktas, Gamze Tanriver, Pierre Quinodoz, Dylan Dagoneau, Amandine Kolleth, Alexandre Lumbroso, Sarah Sulzer-Mossé, Alain De Mesmaeker, Saron Catak
Keteniminium salts (KIs) are versatile intermediates in synthetic organic chemistry. Elucidation of the mechanistic aspects of KI formation reactions facilitates the design of KI intermediates that give access to complex compounds. In this study, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::860b6813b4c1e0866bc78bd74cbe053a
https://doi.org/10.26434/chemrxiv-2022-24jhd
https://doi.org/10.26434/chemrxiv-2022-24jhd
Autor:
Dylan Dagoneau, Pierre Quinodoz, Amandine Kolleth, Mert Bozoflu, Beyza Horoz, Saron Catak, Philippe‐Alexandre Poisson, Alexandre Lumbroso, Sarah Sulzer‐Mossé, Alain De Mesmaeker
Publikováno v:
Helvetica Chimica Acta. 105
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e2cca2597ef167e3822b36b0b813a23
https://doi.org/10.1002/hlca.202100226
https://doi.org/10.1002/hlca.202100226
Autor:
Sarah Sulzer-Mossé, Steven V. Ley, Zebulon G. Levine, Marcus Baumann, Amadeo Fernández, Christof Sparr, Albrecht Metzger, Sabrina Schläger, Ian R. Baxendale
Publikováno v:
Synlett
A new total synthesis of (–)-hennoxazole A is reported. The synthetic approach is based on the preparation of three similarly sized fragments resulting in a fast and convergent assembly of the natural product. The three key reactions of the synthes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::090636a082acbc5fa2ddc1a939cdba47
Autor:
Gamze Tanriver, Alexandre Lumbroso, Amandine Kolleth, Alain De Mesmaeker, Saron Catak, Sarah Sulzer-Mossé
Publikováno v:
ChemInform. 47
We describe an efficient method for the synthesis of aminocyclobutanes via a [2 + 2] cycloaddition between a keteniminium salt and an alkene, followed by a reduction step. The use of easily removable N-allyl moieties as protecting groups increases th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6157ccac269ac3a4e5c52d16b007cf25
https://doi.org/10.1002/chin.201641030
https://doi.org/10.1002/chin.201641030
Autor:
Alexandre Lumbroso, Alain De Mesmaeker, Sarah Sulzer-Mossé, Amandine Kolleth, Saron Catak, Gamze Tanriver
We describe an efficient method for the synthesis of aminocyclobutanes via a [2 + 2] cycloaddition between a keteniminium salt and an alkene, followed by a reduction step. The use of easily removable N-allyl moieties as protecting groups increases th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c3e9a3e2df9b05a5118ceaeded1405
https://aperta.ulakbim.gov.tr/record/54513
https://aperta.ulakbim.gov.tr/record/54513
Autor:
Gérald Bernardinelli, Alexandre Alexakis, Yaroslav Filinchuk, Sarah Sulzer-Mossé, Jiri Mareda, Guillaume Bollot
Publikováno v:
Chemistry-A European Journal, Vol. 15, No 13 (2009) pp. 3204-3220
Chiral framework: Chiral amines with pyrrolidine frameworks catalyze the enantioselective conjugate addition of a wide range of aldehydes to various vinyl sulfones and vinyl phosphonates in high yields and with enantioselectivities up to99 % ee (see
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce77f52244a3aea1f41a4c7d3bf38d97
https://doi.org/10.1002/chem.200801892
https://doi.org/10.1002/chem.200801892
Publikováno v:
ChemInform. 42
Optimized reaction conditions using a novel aminocinchona catalyst and TBA as the additive are developed for the asymmetric condensation of aldehydes with dialkylmalonates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e17c45a15c4f9203dc87e124606237df
https://doi.org/10.1002/chin.201120074
https://doi.org/10.1002/chin.201120074
Publikováno v:
Angewandte Chemie (International ed. in English). 50(7)
Optimized reaction conditions using a novel aminocinchona catalyst and TBA as the additive are developed for the asymmetric condensation of aldehydes with dialkylmalonates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::642e53a4f49e44c89dde48dede097357
https://pubmed.ncbi.nlm.nih.gov/21308938
https://pubmed.ncbi.nlm.nih.gov/21308938
Publikováno v:
Tetrahedron: Asymmetry, Vol. 21, No 13-14 (2010) pp. 1666-1673
Chiral amines with a hydrogen bond donor promote the intramolecular conjugate addition of aldehydes to vinyl sulfones. Chiral cyclic sulfone-aldehydes are obtained in good yields with an ee of up to 82%.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::602a8517e84a691b039f54b8b6e4e990
https://archive-ouverte.unige.ch/unige:11039
https://archive-ouverte.unige.ch/unige:11039