Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Mátyás, Milen"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 653-659 (2022)
New approaches have been tested for the synthesis of lumateperone intermediates. As a result of these efforts, a novel synthesis of the late-stage tetracyclic key intermediate of lumateperone starting from the commercially available quinoxaline is de
Externí odkaz:
https://doaj.org/article/d17b83791c4a444e9567ef12d722146c
Publikováno v:
SynOpen, Vol 03, Iss 04, Pp 148-156 (2019)
Abstract Pimprinols A, B, and C are bacterial 5-(3-indolyl)oxazole alkaloids that have been isolated from Streptomyces sp. Lv3–13. In this paper, we report a new synthesis of pimprinol A and the first total synthesis of pimprinol B and pimprinol C.
Externí odkaz:
https://doaj.org/article/0ab34f6a291b4ed4be5665c811a94886
Autor:
Gábor Györke, András Dancsó, Balázs Volk, László Bezúr, Dávid Hunyadi, Imre Szalóki, Mátyás Milen
Publikováno v:
Catalysis Letters. 153:503-521
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e024beb1b364d736fd6b8c4bb07b86c6
https://doi.org/10.1007/s10562-022-03989-2
https://doi.org/10.1007/s10562-022-03989-2
Publikováno v:
Synthesis. 54:3867-3873
A new total synthesis of the pharmacologically active β-carboline alkaloid brevicolline is described. The new synthetic approach is based on a commercially available and inexpensive starting material and reagents leading to a practical synthesis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a63c22569013cd6d1c08f915339ea2c3
https://doi.org/10.1055/s-0041-1737830
https://doi.org/10.1055/s-0041-1737830
Publikováno v:
Molecules, Vol 26, Iss 3, p 663 (2021)
β-Carboline alkaloids are a remarkable family of natural and synthetic indole-containing heterocyclic compounds and they are widely distributed in nature. Recently, these alkaloids have been in the focus of interest, thanks to their diverse biologic
Externí odkaz:
https://doaj.org/article/1debf065eae643afa95681e810263e85
Publikováno v:
ChemistrySelect. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ef722db81bd6ba0904b5f51a32415cc
https://doi.org/10.1002/slct.202200480
https://doi.org/10.1002/slct.202200480
Publikováno v:
ChemistrySelect. 6:802-807
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f95e45e45df926ddceed0a7b4962fb5
https://doi.org/10.1002/slct.202004596
https://doi.org/10.1002/slct.202004596
Publikováno v:
The Journal of Organic Chemistry. 86:128-145
The synthesis of variously substituted indolo[2,3-c]quinolin-6(7H)-ones was developed via Pd-catalyzed intramolecular C-H arylation. This method highlights a strategy for preparing indoloquinoline precursors bearing versatile functional groups and pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d806979dedb3e7f93656872c75dd2ee9
https://doi.org/10.1021/acs.joc.0c01832
https://doi.org/10.1021/acs.joc.0c01832
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:237-240
In this work, the novel approach via propylphosphonic anhydride (T3P®)-promoted synthesis of 1,5-benzodiazepines from o-phenylene-diamine, 5,5-dimethylcyclohexane-1,3-dione (dimedone), and aromatic aldehydes has been studied. The reaction conditions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::437afa773c7e8d1747bed4f6b4dbc9cf
https://doi.org/10.1007/s10593-020-02650-3
https://doi.org/10.1007/s10593-020-02650-3
Publikováno v:
Tetrahedron Letters. 115:154298
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0537e740b534f0b228a8f644f00df22
https://doi.org/10.1016/j.tetlet.2022.154298
https://doi.org/10.1016/j.tetlet.2022.154298