Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Anne Boussonnière"'
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2020, 85 (14), pp.8933-8943. ⟨10.1021/acs.joc.0c00832⟩
Journal of Organic Chemistry, American Chemical Society, 2020, 85 (14), pp.8933-8943. ⟨10.1021/acs.joc.0c00832⟩
trans-1,2-Cyclohexanediamine, -diether, and -amino ether were compared as chiral inducers in the asymmetric intramolecular carbolithiation of olefinic aryllithiums. Switching from diamine to ethereal ligands inverts the sense of asymmetric induction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8518a89e319837ee359d98a4995d6aac
https://doi.org/10.1021/acs.joc.0c00832
https://doi.org/10.1021/acs.joc.0c00832
Autor:
Hélène Guyon, Anne-Sophie Castanet, Jacques Mortier, Thi Thanh Thuy Nguyen, Anne Boussonnière, Kim Phi Phung Nguyen
Publikováno v:
European Journal of Organic Chemistry. 2020:3829-3833
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be780c06673d9db404f51b95240a496d
https://doi.org/10.1002/ejoc.202000317
https://doi.org/10.1002/ejoc.202000317
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce469a5bf9602c1908a2ae54793c7a66
https://doi.org/10.1002/ejoc.202101409
https://doi.org/10.1002/ejoc.202101409
Autor:
Laurence Pessoni, David Siniscalco, Anne Boussonnière, Anne-Sophie Castanet, Laurent Billon, Nicolas Delorme
Publikováno v:
European Polymer Journal. 174:111297
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa6c2ef0dc224afe756b70e8f38f7e54
https://doi.org/10.1016/j.eurpolymj.2022.111297
https://doi.org/10.1016/j.eurpolymj.2022.111297
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2018, 50 (18), pp.3589-3602. ⟨10.1055/s-0037-1610135⟩
SYNTHESIS, Georg Thieme Verlag, 2018, 50 (18), pp.3589-3602. ⟨10.1055/s-0037-1610135⟩
Organomagnesium reagents are among the most important reagents in organic chemistry because of their great utility in forming carbon–carbon bonds. Although most enantioselective reactions using these organometallics involve transmetalation, the pas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae1edbf53eaadac1aaceb19cb39be1cc
https://doi.org/10.1055/s-0037-1610135
https://doi.org/10.1055/s-0037-1610135
Autor:
Jean-Christophe Rouaud, Carole F. Despiau, Anne Boussonnière, Jacques Lebreton, Fabrice Dénès, Romain Bénéteau
Publikováno v:
Pure and Applied Chemistry
Pure and Applied Chemistry, 2016, 88 (3), pp.215-225. ⟨10.1515/pac-2015-1203⟩
Pure and Applied Chemistry, 2016, 88 (3), pp.215-225. ⟨10.1515/pac-2015-1203⟩
We developed a new approach to γ-lactols and methylene-γ-lactols based upon the radical cyclization of aluminium acetals obtained by reduction of α-bromoesters with DIBAL-H. The cyclic aluminium acetals resulting from the cyclization process could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a4151c1dca68ce885401f62900f585
https://doi.org/10.1515/pac-2015-1203
https://doi.org/10.1515/pac-2015-1203
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (9), pp.4949-4957. ⟨10.1021/acs.joc.7b00423⟩
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (9), pp.4949-4957. ⟨10.1021/acs.joc.7b00423⟩
International audience; A new class of chiral 1,2-amino ether ligands, readily accessible from naturally occurring alpha-amino- or alpha-hydroxy acids, was found to provide high levels of both conversion and stereocontrol (up to 95:5 er) in intramole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8ba03f3f5244364796a7bbdf3608a4a
https://hal.archives-ouvertes.fr/hal-02163261
https://hal.archives-ouvertes.fr/hal-02163261
Autor:
Estelle Banaszak, Kim Phi Phung Nguyen, Anne Boussonnière, Anne-Sophie Castanet, Thi Thanh Thuy Nguyen, Jacques Mortier
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2014, 79 (6), pp.2775-2780. ⟨10.1021/jo500230q⟩
Journal of Organic Chemistry, American Chemical Society, 2014, 79 (6), pp.2775-2780. ⟨10.1021/jo500230q⟩
International audience; Whereas standard strong bases (n-BuLi, s-BuLi/TMEDA, n-BuLi/t-BuOK, TMPMgCl center dot LiCl, and LDA) reduce the N=N bond of the parent azobenzene (Y = H), aromatic H -> Li permutation occurs with LTMP when a suitable director
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59de9fcb32042ed32f1ff445569f2607
https://doi.org/10.1021/jo500230q
https://doi.org/10.1021/jo500230q
Publikováno v:
European Journal of Organic Chemistry. 2013:7853-7866
Aluminum acetals are easily obtained from esters and lactones by reduction with aluminum hydrides. These thermally unstable tetrahedral intermediates have found applications in organic synthesis, with various methodologies taking advantage both of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::738bb3b54386e9e942ca2ef49284f9fd
https://doi.org/10.1002/ejoc.201300624
https://doi.org/10.1002/ejoc.201300624
Autor:
Jean-Christophe Rouaud, Romain Bénéteau, Carole F. Despiau, Jacques Lebreton, Fabrice Dénès, Anne Boussonnière
Publikováno v:
ChemInform. 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6a57a1c2376394c804ad9a169931aa9
https://doi.org/10.1002/chin.201624251
https://doi.org/10.1002/chin.201624251