Yayın: Regio- and diastereoselective synthesis of (E)-3-(2-aminochromen-4-yl)-6-aryl-substituted fulvenes
Dosyalar
Tarih
Kurum Yazarları
Coşkun, Necdet
Yazarlar
Koz, Gamze
Şahin, Onur
Danışman
Dil
Türü
Yayıncı:
Walter de Gruyter Gmbh
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Özet
A practical base-catalyzed route was developed for the regio- and diastereoselective synthesis of (E)-3-aminochromene-6-aryl-disubstituted fulvenes in high yields up to 94% starting with the Michael addition of cyclopentadiene to 2-iminochromenes in the key step.
Açıklama
Kaynak:
Anahtar Kelimeler:
Konusu
Chemistry, Aminochromene, Base catalysis, Cyclopentadiene, Fulvene, Michael addition, Facile synthesis, Michael reaction, Derivatives, 2-amino-4h-chromenes, Cytotoxicity, Inhibitors, Thiourea, Agents, Addition reactions, Catalysis, Olefins, Aminochromene, Base catalysis, Cyclopentadienes, Fulvene, Michael additions, Stereoselectivity, Anticancer drugs
Alıntı
Koz, G. vd. (2016). "Regio- and diastereoselective synthesis of (E)-3-(2-aminochromen-4-yl)-6-aryl-substituted fulvenes". Zeitschrift fur Naturforschung-Section B Journal of Chemical Sciences, 71(9), 945-951.