Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Celia Billaud"'
Autor:
Catherine Willis, Charles Mioskowski, Celia Billaud, Thierry Le Gall, Yann Bourdreux, Ewen Bodio
Publikováno v:
Tetrahedron. 64:8930-8937
A common precursor, tetronic acid, was used in the synthesis of several vulpinic acids and pulvinic acids, which are pigments found in several lichens and mushrooms. The key features of this method are a two-step alkylidenation of benzyl tetronate an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c30710b43eda0c86972dfb8129e51d60
https://doi.org/10.1016/j.tet.2008.06.058
https://doi.org/10.1016/j.tet.2008.06.058
Autor:
Thierry Le Gall, Yann Bourdreux, Catherine Willis, Marine Desage-El Murr, Celia Billaud, Charles Mioskowski, Aurélie Mallinger, Claude Lion, Loïc Toupet, Stéphanie Nowaczyk
Publikováno v:
The Journal of Organic Chemistry. 73:22-26
A short, convergent synthesis of the mushroom pigment norbadione A is described. The construction of an appropriately substituted naphtholactone intermediate involved a regioselective Diels-Alder reaction between a bis(triisopropylsilyloxy)diene and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ad11aa2ba9f5838ae307690a4067df0
https://doi.org/10.1021/jo702106u
https://doi.org/10.1021/jo702106u
Autor:
Yann Bourdreux, Ewen Bodio, Celia Billaud, Thierry Le Gall, Charles Mioskowski, Catherine Willis
Publikováno v:
Tetrahedron Letters. 48:6421-6424
Several vulpinic acids were synthesized in a few steps from a single precursor, the tetronic acid. This commercial compound was converted in a few steps to an iodide. Suzuki–Miyaura cross-couplings involving this common intermediate and various ary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ac721e70be204300153361d59728508
https://doi.org/10.1016/j.tetlet.2007.07.094
https://doi.org/10.1016/j.tetlet.2007.07.094
Publikováno v:
Tetrahedron Letters. 47:5177-5180
CrCl2-mediated condensation of γ-chloro-gem-trichloroalkanes with aldehyde generates homoallylic alcohols through a hydride rearrangement followed by a Nozaki–Hiyama allylation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe40baf56789791dd998f2700329749
https://doi.org/10.1016/j.tetlet.2006.05.045
https://doi.org/10.1016/j.tetlet.2006.05.045
Publikováno v:
Tetrahedron Letters. 44:4451-4454
The reaction of sulfone anions with trialkylboranes followed by thermal isomerization of the obtained boron compounds in the presence of excess borane–methyl sulfide complex and by alkaline hydroperoxide oxidation yields primary alcohols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66723ef8455639fadb7bab1455183007
https://doi.org/10.1016/s0040-4039(03)01025-6
https://doi.org/10.1016/s0040-4039(03)01025-6
Autor:
Marine Desage-El Murr, Claude Lion, Catherine Willis, Celia Billaud, Charles Mioskowski, Loïc Toupet, Stephanie Nowaczyk, Aurélie Mallinger, Thierry Le Gall, Yann Bourdreux
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe13b22f0cc7583779eb4f0c5ea526e3
https://doi.org/10.1002/chin.200820204
https://doi.org/10.1002/chin.200820204
Autor:
Charles Mioskowski, Celia Billaud, Catherine Willis, Thierry Le Gall, Yann Bourdreux, Ewen Bodio
Publikováno v:
ChemInform. 39
Several vulpinic acids were synthesized in a few steps from a single precursor, the tetronic acid. This commercial compound was converted in a few steps to an iodide. Suzuki–Miyaura cross-couplings involving this common intermediate and various ary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58329bba84d1ff94e52ff9937b4d7c3a
https://doi.org/10.1002/chin.200801092
https://doi.org/10.1002/chin.200801092
Autor:
Celia Billaud, T. Le Gall, Claude Lion, Aurélie Mallinger, C. Willis, Y. Bourdreaux, M. Desage-El Murr, Charles Mioskowski, Stéphanie Nowaczyk, L. Toupet
Publikováno v:
Synfacts. 2008:0445-0445
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a3d5b2d5a07a8fb95e1be57ec38b1f4
https://doi.org/10.1055/s-2008-1072702
https://doi.org/10.1055/s-2008-1072702