Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nicolas Brach"'
Publikováno v:
Molecules, Vol 25, Iss 21, p 4976 (2020)
We report herein an efficient synthesis of furopyran derivatives through a gold(I)-catalyzed domino reaction. The cascade reaction starts with two regioselective cyclizations, a 5-endo-dig and a 8-endo-dig, followed with a Grob-type fragmentation and
Externí odkaz:
https://doaj.org/article/f182694021b749a39ee0df126bb91c36
Publikováno v:
Advanced Synthesis & Catalysis. 364:4141-4145
Publikováno v:
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
Comprehensive Heterocyclic Chemistry IV
Reference Module in Chemistry, Molecular Sciences and Chemical Engineering
Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, Elsevier, 2021, ⟨10.1016/B978-0-12-818655-8.00150-5⟩
Comprehensive Heterocyclic Chemistry IV
Reference Module in Chemistry, Molecular Sciences and Chemical Engineering
Reference Module in Chemistry, Molecular Sciences and Chemical Engineering, Elsevier, 2021, ⟨10.1016/B978-0-12-818655-8.00150-5⟩
International audience; Fused and spiro-oxetanes, oxetenes and b-lactones are important classes of compounds that have found numerous applications in various areas of chemistry including medicinal chemistry and total synthesis of natural products. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13111e558fd287fdb746ccbe85e9b633
https://doi.org/10.1016/b978-0-12-818655-8.00150-5
https://doi.org/10.1016/b978-0-12-818655-8.00150-5
Publikováno v:
Molecules
Molecules, MDPI, 2020, 25 (21), pp.4976. ⟨10.3390/molecules25214976⟩
Molecules, Vol 25, Iss 4976, p 4976 (2020)
Molecules, MDPI, 2020, 25 (21), pp.4976. ⟨10.3390/molecules25214976⟩
Molecules, Vol 25, Iss 4976, p 4976 (2020)
International audience; We report herein an efficient synthesis of furopyran derivatives through a gold(I)-catalyzed domino reaction. The cascade reaction starts with two regioselective cyclizations, a 5-endo-dig and a 8-endo-dig, followed with a Gro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f93ae7aec0704c0dacd54e6f1e2d270d
https://hal.archives-ouvertes.fr/hal-02989292/file/molecules-25-04976.pdf
https://hal.archives-ouvertes.fr/hal-02989292/file/molecules-25-04976.pdf
Autor:
Fabrice Gallou, Nicolas Blanchard, Vincent Le Fouler, Nicolas Brach, Vincent Bizet, Michael Parmentier, Corinne Bailly, Marian Lanz, Pascale Hoehn
Publikováno v:
Organic Process Research and Development
Organic Process Research and Development, American Chemical Society, 2020, 24 (5), pp.776-786. ⟨10.1021/acs.oprd.0c00184⟩
Organic Process Research and Development, American Chemical Society, 2020, 24 (5), pp.776-786. ⟨10.1021/acs.oprd.0c00184⟩
International audience; Although pyrimidines are not among the most reactive partners in intramolecular inverse-electron demand [4ps+2ps] reactions with alkynes, they could be activated under mild and practical conditions, leading to fused nitrogen-c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a285471dfc735e6dfcde93149513852
https://hal.archives-ouvertes.fr/hal-02991836
https://hal.archives-ouvertes.fr/hal-02991836
Autor:
Nicolas Brach, Vincent Le Fouler, Vincent Bizet, Marian Lanz, Pascale Hoehn, Fabrice Gallou, Corinne Bailly, Michael Parmentier, Nicolas Blanchard
Although pyrimidines are not among the most reac-tive partners in intramolecular inverse-electron de-mand [4πs+2πs] reactions with alkynes, they could be activated under mild and practical conditions, leading to fused nitrogen-containing heterocycl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12832041587fd803a5f2c2f74e280a4d
https://doi.org/10.26434/chemrxiv.12043989
https://doi.org/10.26434/chemrxiv.12043989