Catalytic aminomethylative etherification of N-allenamides with N,O-acetals enabled by Lewis/Brønsted acid catalysis-Reference-Cited by-同舟云学术

Catalytic aminomethylative etherification of N-allenamides with N,O-acetals enabled by Lewis/Brønsted acid catalysis

Published:2023 Issue:16 Volume:21 Page:3340-3344
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Zhang Tao¹,Ji Danqing¹,Sun Jiangtao¹^ORCID

Affiliation:

1. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China

Abstract

An acid-catalyzed aminomethylative etherification of N-allenamides with N,O-acetals has been achieved under mild reaction conditions.

Funder

Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology Department

Changzhou University

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00363A

Reference34 articles.

1. Catalytic Asymmetric Reactions with N,O-Aminals

2. Catalytic Asymmetric Mannich Reaction with N-Carbamoyl Imine Surrogates of Formaldehyde and Glyoxylate

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4. Palladium-catalyzed formal insertion of carbenoids into N,O-aminals: direct access to α-alkoxy-β-amino acid esters

5. Catalytic Asymmetric and Divergent Synthesis of Tricyclic and Tetracyclic Spirooxindoles: Controllable Site-Selective Electrophilic Halocyclization of 1,6-Enynes