Environmentally Benign Transamidation Protocol for Weakly Nucleophilic Aromatic Amines with <i>N</i> ‐Acyl‐2‐piperidinones: Catalyst‐, Additive‐, Base‐ and Solvent‐Free Condition-Reference-Cited by-同舟云学术

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Environmentally Benign Transamidation Protocol for Weakly Nucleophilic Aromatic Amines with N ‐Acyl‐2‐piperidinones: Catalyst‐, Additive‐, Base‐ and Solvent‐Free Condition

Published:2022-08-18 Issue:9 Volume:11 Page:
ISSN:2193-5807
Container-title:Asian Journal of Organic Chemistry
language:en
Short-container-title:Asian J Org Chem

Author:

Rajan Ida Angel Priya Samuel¹,Subramani Muthuraman¹,Pushparathinam Gopinath²,Rajendran Saravanakumar¹^ORCID

Affiliation:

1. Chemistry Division Vellore Institute of Technology Chennai campus Vandalur-Kelambakkam road 600127 Chennai Tamil Nadu India

2. Department of Chemistry College of Engineering and Technology SRM Institute of Science and Technology Kattankulathur 603203 Chennai Tamil Nadu India

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.202200378

Reference46 articles.

1. Acyclic Twisted Amides

2. Amide Synthesis by Transamidation of Primary Carboxamides

3. Non-Classical Amide Bond Formation: Transamidation and Amidation of Activated Amides and Esters by Selective N–C/O–C Cleavage

4. Transamidation of N-acyl-glutarimides with amines

5. Amide Bond Activation: The Power of Resonance

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1. Ring Opening of N-Acyl Lactams Using Nickel-Catalyzed Transamidation;The Journal of Organic Chemistry;2024-01-04

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