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A transition-metal-free multicomponent reaction towards constructing chiral 2 H -1,4-benzoxazine scaffolds
Herein, a transition-metal-free multicomponent cascade reaction of readily available α-halogenated ketones, ortho -aminophenols, and aldehydes using a novel dipeptide-based phosphonium salt catalyst was developed for the efficient construction of various 2 H -1,4-benzoxazine derivatives with excelle...
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Published in: | Green chemistry : an international journal and green chemistry resource : GC 2020-11, Vol.22 (21), p.7506-7512 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Herein, a transition-metal-free multicomponent cascade reaction of readily available α-halogenated ketones,
ortho
-aminophenols, and aldehydes using a novel dipeptide-based phosphonium salt catalyst was developed for the efficient construction of various 2
H
-1,4-benzoxazine derivatives with excellent functional-group tolerance. The method represents an unprecedented approach for trapping active 1,5-bifunctional intermediates with α-halogenated ketones to access biologically important benzoxazine scaffolds bearing two stereogenic centers with excellent asymmetric induction. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/D0GC02134B |