Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Aïda R. Nadji-Boukrouche"'
Publikováno v:
Molecules, Vol 20, Iss 1, Pp 1262-1276 (2015)
We describe an original pathway to produce new 5-substituted 3-methyl-6-nitro-benzoxazolones by the reaction of aromatic carbonyl and α-carbonyl ester derivatives with a benzoxazolinonic anion formed exclusively via the TDAE strategy.
Externí odkaz:
https://doaj.org/article/faafbc05557e4ee7ae84386e96d0dcd7
Publikováno v:
ARKIVOC, Vol 2010, Iss 10, Pp 358-370 (2010)
Externí odkaz:
https://doaj.org/article/c46f5e7794df47759d4415a64dcc60cf
Publikováno v:
ChemInform. 46
One-pot Sonogashira-cyclization reaction of bromoquinone (I) and propargyl alcohol provides benzo[f]indole-4,9-diones (III) and (IV).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5533200fe86b8438ca10286867caf526
https://doi.org/10.1002/chin.201532136
https://doi.org/10.1002/chin.201532136
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2015, 56 (17), pp.2272--2275. ⟨10.1016/j.tetlet.2015.03.074⟩
Tetrahedron Letters, 2015, 56 (17), pp.2272--2275. ⟨10.1016/j.tetlet.2015.03.074⟩
Tetrahedron Letters, Elsevier, 2015, 56 (17), pp.2272--2275. ⟨10.1016/j.tetlet.2015.03.074⟩
Tetrahedron Letters, 2015, 56 (17), pp.2272--2275. ⟨10.1016/j.tetlet.2015.03.074⟩
International audience; A new series of 1-methyl-1H-benzo[f]indole-4,9-dione derivatives was prepared via a one-pot 'Sonogashira-Cyclization' reaction with propagylic alcohol in the presence of a palladium catalyst leading to regio-isomers of 2- and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a176abda9a08dae9a1328542de2d616
https://hal-amu.archives-ouvertes.fr/hal-01460642
https://hal-amu.archives-ouvertes.fr/hal-01460642
Publikováno v:
ARKIVOC-Online Journal of Organic Chemistry
ARKIVOC-Online Journal of Organic Chemistry, 2010, Part 10, pp.358-370. ⟨10.3998/ark.5550190.0011.a30⟩
ARKIVOC, Vol 2010, Iss 10, Pp 358-370 (2010)
Arkivoc
Arkivoc, 2010, pp.358--370
ARKIVOC-Online Journal of Organic Chemistry, 2010, Part 10, pp.358-370. ⟨10.3998/ark.5550190.0011.a30⟩
ARKIVOC, Vol 2010, Iss 10, Pp 358-370 (2010)
Arkivoc
Arkivoc, 2010, pp.358--370
International audience; We present herein an extension of the TDAE strategy using original heterocyclic carbaldehyde as electrophiles. We also evaluate the influence of the presence of nitro group on the reactivity. The TDAE-initiated reactions of va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6284207f08299cb1fac39d40f0d5a4a1
https://hal.science/hal-01460247
https://hal.science/hal-01460247