Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Monireh Pourghasemi Lati"'
Publikováno v:
Molecules, Vol 25, Iss 2, p 361 (2020)
Herein, we present a short and highly modular synthetic route that involves 8-aminoquinoline directed C−H arylation and transamidation chemistry, and which enables access to a wide range of elaborate benzofuran-2-carboxamides. For the directed C−
Externí odkaz:
https://doaj.org/article/8aa99d88a14741a293dd835d9dbb18bd
Publikováno v:
Journal of Nanoscience and Nanotechnology. 20:973-982
A green, simple and eco-friendly procedure for the preparation of 3,4-dihydropyrano[c]chromenes and 2-amino-4H-chromene derivatives is described using Fe₃O₄@SiO₂-Sultone as a novel and efficient magnetic nanocatalyst. All reactions are performe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a93712251cf43c3b959ddc15322599f
https://doi.org/10.1166/jnn.2020.16890
https://doi.org/10.1166/jnn.2020.16890
Publikováno v:
The Journal of Organic Chemistry
This work outlines a synthetic route that can be used to access chiral cyclobutane keto acids with two stereocenters in five steps from the inexpensive terpene myrtenal. Furthermore, the developed route includes an 8-aminoquinoline-directed C(sp2)–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0654b916f9d568fddae3a42c2b2d3bc5
https://pubmed.ncbi.nlm.nih.gov/34042431
https://pubmed.ncbi.nlm.nih.gov/34042431
Autor:
Aaltje Roelofje Femmigje Strijker, Monireh Pourghasemi Lati, Michael Oschmann, Aleksandra Balliu, Oscar Verho
In this preprint, we present our initial results concerning a stereospecific Pd-catalyzed protocol for the C3 alkenylation and alkynylation of a proline derivative carrying the well utilized 8‑aminoquinoline directing group. Efficient C–H alkenyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c1a029afb594d8719d9f3d066dceb93
https://doi.org/10.26434/chemrxiv.12034743.v1
https://doi.org/10.26434/chemrxiv.12034743.v1
Autor:
Oscar Verho, Monireh Pourghasemi Lati, Muhammad Iqbal Naeem, Eric V. Johnston, Mokhtar Alinia-Asli, Farhad Shirini, Mohammad Ali Rezvani, Björn Åkermark
Publikováno v:
ChemistrySelect. 3:7970-7975
Herein, we describe the straightforward synthesis and thorough characterization of a magnetically-separable heterogeneous catalyst comprised of 1-3nm-sized Pd nanoparticles immobilized on a mesopor ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b0c263c13d0413ed4b4563372422657
https://doi.org/10.1002/slct.201801415
https://doi.org/10.1002/slct.201801415
Publikováno v:
Journal of the Iranian Chemical Society. 15:1655-1662
4-(4-Propylpiperazine-1-yl)butane-1-sulfonic acid-modified silica-coated magnetic nanoparticles have been synthesized via covalent grafting of piperazine on (3-chloropropyl) triethoxysilane-functionalized magnetic nanoparticles through ring opening r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27566519ed9cd50ff40f2abf67ba6388
https://doi.org/10.1007/s13738-018-1364-5
https://doi.org/10.1007/s13738-018-1364-5
Publikováno v:
The Journal of Organic Chemistry. 83:4464-4476
Herein a two-step strategy for achieving overall transamidation of 8-aminoquinoline amides has been explored. In this protocol, the 8-aminoquinoline amides were first treated with Boc2O and DMAP to form the corresponding N-acyl-Boc-carbamates, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d504776ea5fcf726402e288725678c42
https://doi.org/10.1021/acs.joc.8b00174
https://doi.org/10.1021/acs.joc.8b00174
Publikováno v:
Journal of the Iranian Chemical Society. 14:75-87
BiVO4-NPs can be used as an efficient and reusable nano-catalyst for the promotion of the synthesis of biscoumarins, bis(indolyl)methanes and 3,4-dihydropyrimidin-2(1H)-ones (thiones) derivatives. The structures of the products were characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2041e490bd09c71f529dbfd33f7f93b3
https://doi.org/10.1007/s13738-016-0959-y
https://doi.org/10.1007/s13738-016-0959-y