Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Leyla Pehlivan"'
Autor:
Estelle Métay, Wissam Dayoub, Leyla Pehlivan, Dominique Delbrayelle, Gerard Mignani, Stephane Laval, Marc Lemaire, Alain Favre-Réguillon
Publikováno v:
Tetrahedron. 70:975-983
1,1,3,3-Tetramethyldisiloxane (TMDS) and polymethylhydrosiloxane (PMHS), when associated with titanium(IV) isopropoxide, provide two convenient systems for the reduction of nitriles into the corresponding primary amines. Kinetics of the two systems h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61cfe5077854d20c2faa8fbd48ed7bdf
https://doi.org/10.1016/j.tet.2013.11.101
https://doi.org/10.1016/j.tet.2013.11.101
Publikováno v:
Tetrahedron. 68:3151-3155
An efficient method for the reduction of phosphine oxide derivatives into their corresponding phosphines is described. The system InBr3/TMDS allows the reduction of different secondary and tertiary phosphine oxides as well as aliphatic and aromatic p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9df761ee607e38a2d35eeac9f9b8614a
https://doi.org/10.1016/j.tet.2012.02.063
https://doi.org/10.1016/j.tet.2012.02.063
Publikováno v:
Tetrahedron Letters. 52:4720-4723
This Letter describes a highly diastereoselective synthesis of the unique 1-hydroxy endo,endo-2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane skeleton starting from a stereodefined 4-arylidenetetrahydrofuran obtained by a multicomponent reaction. The key st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::001142857b588a0514b05c6bc9bbd829
https://doi.org/10.1016/j.tetlet.2011.07.014
https://doi.org/10.1016/j.tetlet.2011.07.014
Autor:
Maïwenn Jacolot, Nicolas Coia, Nuno Monteiro, Geneviève Balme, Leyla Pehlivan, Didier Bouyssi
Publikováno v:
Tetrahedron Letters. 52:4716-4719
A dealkylative lactonization of stereodefined aryl-substituted epoxides allows the preparation of densely functionalized fused δ-hydroxy-γ-lactones having three consecutive stereochemically defined stereocenters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d097541995cd5ad871fc8bd45ae7ee4
https://doi.org/10.1016/j.tetlet.2011.06.106
https://doi.org/10.1016/j.tetlet.2011.06.106
Autor:
Leyla Pehlivan, Marc Lemaire, Alain Favre-Réguillon, Gerard Mignani, Estelle Metay, Wissam Dayoub, Dominique Delbrayelle, Stephane Laval
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2011, 52 (32), pp.4072-4075. ⟨10.1016/j.tetlet.2011.05.109⟩
Tetrahedron Letters, Elsevier, 2011, 52 (32), pp.4072-4075. ⟨10.1016/j.tetlet.2011.05.109⟩
International audience; A simple and useful method for the reduction of primary amides into the corresponding amines using a polymethylhydrosiloxane (PMHS)–Ti(OiPr)4 reducing system is described. Aromatic as well as aliphatic primary amides are red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa7402cdcb404768940feb77e3115778
https://doi.org/10.1016/j.tetlet.2011.05.109
https://doi.org/10.1016/j.tetlet.2011.05.109
Autor:
Gerard Mignani, Olivier Boyron, Estelle Metay, Marc Lemaire, Patrice Demonchaux, Leyla Pehlivan
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2011, 24, pp.4687-4692
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2011, 24, pp.4687-4692
International audience; The 1,1,3,3-tetramethyldisiloxane/Pd/C system is reported here as a new method to accomplish the ring-opening of ethers and epoxides to give protected alcohols. The approach can also be used for the protection of primary or se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f169af1b7a7d5c2e404768ce38c0395
https://doi.org/10.1002/ejoc.201100489
https://doi.org/10.1002/ejoc.201100489
Autor:
Wissam Dayoub, Gerard Mignani, Dominique Delbrayelle, Stephane Laval, Marc Lemaire, Alain Favre-Réguillon, Leyla Pehlivan, Estelle Métay
Publikováno v:
ChemInform. 45
The presented two titanium-based systems reduce aliphatic and aromatic nitriles in the presence of various functional groups.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c950393964bc67e7a0ca7e2e05e188b
https://doi.org/10.1002/chin.201429042
https://doi.org/10.1002/chin.201429042
Autor:
Stephane Laval, Gerard Mignani, Wissam Dayoub, Leyla Pehlivan, Marc Lemaire, Estelle Métay, Dominique Delbrayelle
Publikováno v:
ChemInform. 45
A simple and convenient method for the chemoselective reduction of nitriles into aldehydes using a 1,1,3,3-tetramethyldisiloxane (TMDS)/triisopropoxyvanadium(V) oxide reducing system is described. Aromatic as well as aliphatic nitriles are reduced in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22fd2f19a13c96649b5441489a453cb2
https://doi.org/10.1002/chin.201420065
https://doi.org/10.1002/chin.201420065
Autor:
Marc Lemaire, Leyla Pehlivan, Romain Lafon, Estelle Metay, Marc Sutter, Wissam Dayoub, Yann Raoul
Publikováno v:
ChemInform. 45
1,2,3-Trimethoxypropane (1,2,3-TMP) was prepared from glycerol in one step in good yield and selectivity by phase transfer catalysis. According to OECD guidelines, a toxicity study was realized for this compound. It revealed that 1,2,3-TMP has a low
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cf9ee01ad747940e938c1ed9baec46b
https://doi.org/10.1002/chin.201413039
https://doi.org/10.1002/chin.201413039
Autor:
Estelle Métay, Gerard Mignani, Wissam Dayoub, Stephane Laval, Leyla Pehlivan, Marc Lemaire, Dominique Delbrayelle
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2014, 55 (1), pp.23-26
Tetrahedron Letters, Elsevier, 2014, 55 (1), pp.23-26
International audience; A simple and convenient method for the chemoselective reduction of nitriles into aldehydes using a 1,1,3,3-tetramethyldisiloxane (TMDS)/triisopropoxyvanadium(V) oxide reducing system is described. Aromatic as well as aliphatic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::659340f15fbe14dc0567602ec65f9484
https://hal.archives-ouvertes.fr/hal-01149127
https://hal.archives-ouvertes.fr/hal-01149127
