Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Gurunathan Savitha"'
Publikováno v:
Tetrahedron Letters. 57:5168-5178
Chiral nanoparticles have become one of the most versatile catalyst for the effective construction of chiral organic moieties. Recently, bimetallic nanoparticles as catalysts have gained interest among the chemists. The presence of hetero metal–met
Publikováno v:
Chemistry-An Asian Journal
Chemistry-An Asian Journal, Wiley-VCH Verlag, 2017, 12 (15), pp.1935-1943. ⟨10.1002/asia.201700545⟩
Chemistry-An Asian Journal, Wiley-VCH Verlag, 2017, 12 (15), pp.1935-1943. ⟨10.1002/asia.201700545⟩
International audience; 3-Hexyloxy-4-cyanothiophene, 3-pyrrolidil-4-cyanothiophene, and 3,4-ethylenedioxythiophene (EDOT) units are used with benzothiadiazole as building blocks for the development of three new conjugated donor–acceptor–donor (DA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::351d62a0d0aa4b453ef11ec9cf3d7377
https://hal.univ-angers.fr/hal-02564420
https://hal.univ-angers.fr/hal-02564420
Publikováno v:
ChemInform. 47
Chiral nanoparticles have become one of the most versatile catalyst for the effective construction of chiral organic moieties. Recently, bimetallic nanoparticles as catalysts have gained interest among the chemists. The presence of hetero metal–met
Autor:
Gurunathan Savitha, Frédéric Gohier, Charlotte Mallet, Pierre Frère, Magali Allain, Jérémie Grolleau, Simon Olivier, Chady Moussallem
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2016, 22 (19), pp.6510-6514. ⟨10.1002/chem.201600159⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2016, 22 (19), pp.6510-6514. ⟨10.1002/chem.201600159⟩
International audience; Aromatization of 4-cyano-3-oxotetrahydrothiophene by sulfuryl chloride gives the new building block 4-cyano-3-pyrrolidylthiophene, which forms unsymmetrical regioregular oligothiophenes with a strict alternation of the donor a
Publikováno v:
Chemistry - An Asian Journal. 12:1838-1838
Autor:
Charlotte Mallet, Jiří Svoboda, Gurunathan Savitha, Pierre Frère, Václav Kozmík, Jean Roncali, Magali Allain
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2012, 77 (4), pp.2041-2046. ⟨10.1021/jo202412t⟩
Journal of Organic Chemistry, American Chemical Society, 2012, 77 (4), pp.2041-2046. ⟨10.1021/jo202412t⟩
3-Alkoxy-4-cyanothiophene units are used as building block for the synthesis of conjugated donor-acceptor-donor (D-A-D) triads. The donor part consists of benzothienothiophene end groups associated with the alkoxy groups of the 3-alkoxy-4-cyanothioph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61493c3e63a1360c753f49b7be42097b
https://hal.univ-angers.fr/hal-03344594
https://hal.univ-angers.fr/hal-03344594
Autor:
Jean Roncali, Pierre Frère, Noémie Hergué, Charlotte Mallet, Gurunathan Savitha, Magali Allain
Publikováno v:
ChemInform. 42
The title compounds (IV) are prepared by selective O-alkylation of the intermediate enolate anion of (I) followed by oxidation with DDQ.
Autor:
Noémie Hergué, Charlotte Mallet, Gurunathan Savitha, Magali Allain, Jean Roncali, Pierre Frère
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2011, 13 (7), pp.1762-1765. ⟨10.1021/ol200296j⟩
Organic Letters, American Chemical Society, 2011, 13 (7), pp.1762-1765. ⟨10.1021/ol200296j⟩
3-Alkoxy-4-cyanothiophenes are efficiently synthesized in two steps from the readily available 4-cyano-3-oxotetrahydrothiophene. Regioisomers of bithiophene derivatives are easily synthesized by playing on the strong electronic dissymmetry of the thi
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2011, 52 (12), pp.1288-1291. ⟨10.1016/j.tetlet.2011.01.050⟩
Tetrahedron Letters, Elsevier, 2011, 52 (12), pp.1288-1291. ⟨10.1016/j.tetlet.2011.01.050⟩
International audience; 3-Alkoxy-4-bromothiophenes were synthesized in three steps from the readily available methyl 2-carboxylate-3-hydroxythiophene and two isomers of bithiophenes based on the 3-bromo-4-methoxythiophene moiety were regio-selectivel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e713caff917396f5b18ba07cb0a217fd
https://hal.univ-angers.fr/hal-03344598
https://hal.univ-angers.fr/hal-03344598
Publikováno v:
In Tetrahedron Letters 2011 52(15):1783-1787