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pro vyhledávání: '"Granulatimide"'
Akademický článek
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Publikováno v:
Marine Drugs, Vol 7, Iss 4, Pp 754-786 (2009)
Granulatimide and isogranulatimide are alkaloids obtained from marine sources which have been shown to inhibit cell-cycle G2-checkpoint, targeting more particularly checkpoint 1 kinase (Chk1). At a structural level, they possess a characteristic pyrr
Externí odkaz:
https://doaj.org/article/fda0af8898ac4925b406c6ed94e4ed6d
Publikováno v:
The 23rd International Electronic Conference on Synthetic Organic Chemistry.
Pyrrolocarbazoles are important structural motives present in many natural products and pharmaceuticals. Particularly, pyrrolo [3,4-a] carbazole-1,3-diones have attracted much attention as analogues of bioactive compounds, such as anticancer agent gr
Publikováno v:
Synthesis. 47:3573-3582
An efficient copper-catalyzed π-activation protocol has been developed for the intramolecular hydroarylation of alkynes. The strategy has been used in atom-economical syntheses of β-carboline analogues. The cycloisomerized products were obtained in
Publikováno v:
Marine Drugs
Marine Drugs, Vol 7, Iss 4, Pp 754-786 (2009)
Marine Drugs, Vol 7, Iss 4, Pp 754-786 (2009)
Granulatimide and isogranulatimide are alkaloids obtained from marine sources which have been shown to inhibit cell-cycle G2-checkpoint, targeting more particularly checkpoint 1 kinase (Chk1). At a structural level, they possess a characteristic pyrr
Publikováno v:
ChemInform. 47
An efficient copper-catalyzed π-activation protocol has been developed for the intramolecular hydroarylation of alkynes. The strategy has been used in atom-economical syntheses of β-carboline analogues. The cycloisomerized products were obtained in
Autor:
Bruno Pfeiffer, Armelle Loynel, Nathalie Kucharczyk, Hélène Henon, Fabrice Anizon, Patrick Casara, Michelle Prudhomme
Publikováno v:
Synthesis. 2006:711-715
Dipyrrolo[3,4-a:3,4-c]carbazole-1,3,4,6-tetraones can be considered as granulatimide analogues. In view of structure-activity relationship studies in these series, a parallel liquid-phase microwave-assisted synthesis was developed to generate a small
Akademický článek
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Autor:
Bruno Pfeiffer, Fabrice Anizon, Bernadette Hugon, Michelle Prudhomme, Samir Messaoudi, Hélène Henon
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2005, 61, pp.5599-5614. ⟨10.1016/j.tet.2005.03.101⟩
Tetrahedron, 2005, 61, pp.5599-5614. ⟨10.1016/j.tet.2005.03.101⟩
Tetrahedron, Elsevier, 2005, 61, pp.5599-5614. ⟨10.1016/j.tet.2005.03.101⟩
Tetrahedron, 2005, 61, pp.5599-5614. ⟨10.1016/j.tet.2005.03.101⟩
The synthesis of dipyrrolo[3,4-a:3,4-c]carbazole-1,3,4,6-tetraones, structurally related to granulatimide is reported. These compounds can be considered as granulatimide analogues in which a maleimide heterocycle replaces the imidazole moiety. The sy
Publikováno v:
Chemical and Pharmaceutical Bulletin. 50:872-876
The Stille coupling reaction of stannylindole 12 with 4-iodoimidazole 13 (or 24) in the presence of PdCl(2)(PPh(3))(2) gave the corresponding indole-imidazole coupling product 14 (or 25), thereby affording a new synthetic approach to the alkaloid gra