Synthesis of Chiral 2-Substituted 1,4-Benzoxazin-3-ones via Iridium-Catalyzed Enantioselective Hydrogenation of Benzoxazinones.

Org Lett

Shanghai Key Laboratory of Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P. R. China.

Published: July 2021

An efficient iridium-catalyzed enantioselective hydrogenation of 2-alkylidene 1,4-benzoxazin-3-ones using our developed Pr-BiphPHOX as a ligand is reported. This method showed good functional group compatibility and delivered the corresponding reduced products in excellent yields (up to 99%) with excellent enantioselectivities (up to 99% ee). The reaction proceeded very well on a gram scale with low catalyst loadings (0.1 mol %), providing the product with no erosion in enantioselectivity. Additionally, three bioactive molecules can be easily obtained from the reduced products.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.orglett.1c01701DOI Listing

Publication Analysis

Top Keywords

iridium-catalyzed enantioselective
8
enantioselective hydrogenation
8
reduced products
8
synthesis chiral
4
chiral 2-substituted
4
2-substituted 14-benzoxazin-3-ones
4
14-benzoxazin-3-ones iridium-catalyzed
4
hydrogenation benzoxazinones
4
benzoxazinones efficient
4
efficient iridium-catalyzed
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!