NDLI: Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones

Content Provider	Semantic Scholar
Author	Rueping, Magnus Moreth, Stefan A. Bolte, Michael
Copyright Year	2012
Abstract	The enantioselective synthesis of 2-aryl-substituted 2,3-dihydroquinolin-4-ones, a class of heterocyclic compounds with interesting biological activities, has been achieved through a Brønsted acidcatalyzed enantioselective intramolecular Michael addition. The products are available in moderate to high yields and with good enantioselectivities. Graphical Abstract Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones
Starting Page	1021
Ending Page	1029
Page Count	9
File Format	PDF HTM / HTML
DOI	10.5560/znb.2012-0183
Volume Number	67
Alternate Webpage(s)	http://www.znaturforsch.com/s67b/s67b1021.pdf
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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