Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Philippe Bisseret"'
Publikováno v:
European Journal of Organic Chemistry. 2017:6816-6830
Nitrogen-substituted alkynes such as ynamines and ynamides are competent partners in [4+2] cycloaddition reactions. This microreview aims to discuss in a historical context the main achievements in the work on this class of reactions that leads to va
Publikováno v:
Comptes Rendus. Chimie
Comptes Rendus. Chimie, Académie des sciences (Paris), 2017, 20 (6), pp.643-647. ⟨10.1016/j.crci.2017.01.007⟩
Comptes Rendus. Chimie, Académie des sciences (Paris), 2017, 20, pp.643-647
doi.org/10.1016/j.crci.2017.01.007
Comptes Rendus. Chimie, Académie des sciences (Paris), 2017, 20 (6), pp.643-647. ⟨10.1016/j.crci.2017.01.007⟩
Comptes Rendus. Chimie, Académie des sciences (Paris), 2017, 20, pp.643-647
doi.org/10.1016/j.crci.2017.01.007
International audience; Three representative 6,7-dihydro-5H-cyclopenta[b]pyridin-4-amines were synthesized using an intramolecular inverse electron demand heteroeDielseAlder/retroeDielseAlder sequence between pyrimidines (acting as azadienes) and yna
Autor:
Cédric Tresse, Philippe Bisseret, Jacques Lalevée, Nicolas Blanchard, Gwilherm Evano, Stéphane Schweizer
Publikováno v:
Synthesis. 48:3317-3330
Stereoselective hydrometalation reactions of aryl- and alkyl-substituted trifluoromethylated alkynes with triethylsilane, tributylstannane, and triphenylgermane have been investigated. (E)-α-CF3-Vinylsilanes, -stannanes, and -germanes were obtained
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2018, 59 (36), pp.3349-3352. ⟨10.1016/j.tetlet.2018.07.053⟩
Tetrahedron Letters, Elsevier, 2018, 59 (36), pp.3349-3352. ⟨10.1016/j.tetlet.2018.07.053⟩
Ynamides are versatile 3-atoms building blocks for organic synthesis as they participate in a variety of ionic, radical and pericyclic processes. Converting ynamides into 5-atom building blocks, such as the yet unreported N-vinyl ynamides, would open
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::292be67be0a5304101f0a776255f4e75
https://hal.archives-ouvertes.fr/hal-02159670
https://hal.archives-ouvertes.fr/hal-02159670
Publikováno v:
Chemical Science
Chemical Science, The Royal Society of Chemistry, 2018, 9, pp.5132-5144. ⟨10.1039/C8SC00780B⟩
Chemical Science, The Royal Society of Chemistry, 2018, 9, pp.5132-5144. ⟨10.1039/C8SC00780B⟩
Bioorthogonal organometallic chemistry using aryl transition metal reagents as coupling partners is a burgeoning field that holds great promise notably for the study of proteins.
The past seven years have witnessed the burgeoning of protein bioc
The past seven years have witnessed the burgeoning of protein bioc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb3fb3a62f656a2f44fa086e9b15f59a
https://hal.archives-ouvertes.fr/hal-02153059/document
https://hal.archives-ouvertes.fr/hal-02153059/document
Publikováno v:
Chemical Science
Activation of stable boron species with visible-light allows the creation of boryl and/or carbon radicals through single electron- or energy transfer.
Photocatalysis has recently opened up new avenues for the generation of radical species under
Photocatalysis has recently opened up new avenues for the generation of radical species under
Autor:
Sarah, Saint-Auret, Hajer, Abdelkafi, Didier, Le Nouen, Laure, Guenin-Macé, Caroline, Demangel, Philippe, Bisseret, Nicolas, Blanchard
Publikováno v:
Organicbiomolecular chemistry. 15(36)
A modular total synthesis of mycolactone A/B, the exotoxin produced by Mycobacterium ulcerans, has been achieved through the orchestration of several Pd-catalyzed key steps. While this route leads to a mixture of the natural product and its C12 epime
Autor:
Caroline Demangel, Nicolas Blanchard, Sarah Saint-Auret, Didier Le Nouen, Philippe Bisseret, Hajer Abdelkafi, Laure Guenin-Macé
Publikováno v:
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2017, 15, pp.7518-7522. ⟨10.1039/C7OB01943B⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2017, 15, pp.7518-7522. ⟨10.1039/C7OB01943B⟩
Organic & Biomolecular Chemistry, 2017, 15, pp.7518-7522. ⟨10.1039/C7OB01943B⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2017, 15, pp.7518-7522. ⟨10.1039/C7OB01943B⟩
A modular total synthesis of mycolactone A/B, the exotoxin produced by Mycobacterium ulcerans, has been achieved through the orchestration of several Pd-catalyzed key steps. While this route leads to a mixture of the natural product and its C12 epime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ae34d983f0c9589d964859b15030d2
https://hal-pasteur.archives-ouvertes.fr/pasteur-01666631
https://hal-pasteur.archives-ouvertes.fr/pasteur-01666631
Autor:
Guillaume Duret, Philippe Bisseret, Nicolas Blanchard, Vincent Gandon, Robert Quinlan, Rainer E. Martin, Boyang Yin, Markus Neuburger
4-Aminopyridines are valuable scaffolds for the chemical industry in general, from life sciences to catalysis. We report herein a collection of structurally diverse polycyclic fused and spiro-4-aminopyridines that are prepared in only three steps fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::076dd807a19080e1265ac8efb931c8eb
Publikováno v:
Organic Chemistry Frontiers
Organic Chemistry Frontiers, Royal Society of Chemistry, 2017, 4, pp.2380-2386. ⟨10.1039/C7QO00608J⟩
Organic Chemistry Frontiers, Royal Society of Chemistry, 2017, 4, pp.2380-2386. ⟨10.1039/C7QO00608J⟩
Mycolactone A/B, a complex polyketidic macrolide secreted by Mycobacterium ulcerans, has been synthesized using catalytic and/or asymmetric reactions. Several palladium-catalyzed reactions were investigated for forging key σ-bonds as well as a parti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7e8e33f02c844733c475894bdaf5284
https://hal.archives-ouvertes.fr/hal-02153057
https://hal.archives-ouvertes.fr/hal-02153057