Herein we demonstrate a novel organocatalytic method to access multifunctionalized naphthalenes an NHC-catalyzed reaction of ynones and -formyl-tethered Michael acceptors. The presented method proceeds through an intermolecular Stetter reaction-cyclization-aromatization cascade and represents a rare example of organocatalytic benzannulation for the synthesis of substituted arenes by using ynone as a two-carbon synthon. The current method has broad substrate scope; postsynthetic transformations and gram-scale syntheses highlight the practicality of the displayed methodology.
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http://dx.doi.org/10.1021/acs.orglett.3c04249 | DOI Listing |
J Org Chem
November 2024
Department of Chemistry, Indian Institute of Science Education and Research (IISER) Bhopal, Bhopal 462066, India.
Herein, we disclose a cinchona-alkaloid-based squaramide-catalyzed intermolecular oxa-Michael cascade addition cyclization of -protected hydroxyl amine to formyl-tethered Michael acceptors toward the synthesis of enantioenriched 1,2-oxazine scaffolds. Generally, good yield (up to 78%), good to excellent enantiomeric ratio (up to 98:2 er), and excellent regioselectivity (>19:1) were observed. Furthermore, the scalability of this methodology and a successful demonstration of postsynthetic transformations have been accomplished.
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