A versatile switching method for N- or O-alkylation of 2-aminophenols using ionic liquids: Selective access to benzo[1,4]oxazine-2-one and benzo[1,4]oxazine-3-one derivatives-Reference-Cited by-同舟云学术

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A versatile switching method for N- or O-alkylation of 2-aminophenols using ionic liquids: Selective access to benzo[1,4]oxazine-2-one and benzo[1,4]oxazine-3-one derivatives

Published:2023-08 Issue: Volume:126 Page:154643
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Shabpiray Mohammad^ORCID,Sharifi Ali^ORCID,Abaee M. Saeed,Mirzaei Moitaba,Ghonouei Nima

Funder

Norges Forskningsråd

Chemistry and Chemical Engineering Research Center of Iran

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference36 articles.

1. Ready N-alkylation of enantiopure aminophenols: synthesis of tertiary aminophenols

2. Asymmetric PTC C-Alkylation Catalyzed by Chiral Derivatives of Tartaric Acid and Aminophenols. Synthesis of (R)- and (S)-α-Methyl Amino Acids

3. Synthesis of Multisubstituted 1,4-Dihydrobenzoxazin-2-ones through a One-Pot Nucleophilic N-Alkylation/C-Alkylation of Cyclic α-Imino Esters

4. Microwave-assisted one-pot regioselective synthesis of 2-alkyl-3,4-dihydro-3-oxo-2H-1,4-benzoxazines

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Green synthesis of 1,4-benzoxazin-3-one using a choline chloride based deep eutectic solvent;Arkivoc;2024-06-03

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