A General Method to Access Underexplored Ylideneamino Sulfates as Interrupted Beckmann-Type Rearrangement Intermediates
The Beckmann rearrangement of ketoximes to their corresponding amides, using a Brønsted acid-mediated fragmentation and migration sequence, has found wide-spread industrial application. We postulated that the development of a methodology to access ylideneamino sulfates using tributylsulfoammonium be...
Main Authors: | Yifei Zhou, Alan M. Jones |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2024-04-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/29/7/1667 |
Similar Items
-
Synthesis of a tricyclic lactam via Beckmann rearrangement and ring-rearrangement metathesis as key steps
by: Sambasivarao Kotha, et al.
Published: (2015-08-01) -
Beckmann Rearrangement of Ketoxime Catalyzed by N-methyl-imidazolium Hydrosulfate
by: Hongyu Hu, et al.
Published: (2018-07-01) -
SYNTHESIS OF NEW DRIMANE AND HOMODRIMANE LACTAMS BY BECKMANN REARRANGEMENT OF SOME KETOXIMES
by: Elena Secara
Published: (2016-06-01) -
Approaches to α-amino acids via rearrangement to electron-deficient nitrogen: Beckmann and Hofmann rearrangements of appropriate carboxyl-protected substrates
by: Sosale Chandrasekhar, et al.
Published: (2012-08-01) -
Photochemical and Beckmann rearrangement of (Z)-cholest-4-en-6-one oxime
by: VLADIMIR D. PAVLOVIC, et al.
Published: (2004-06-01)