Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones
Reaction of 1,3-di-tert-butylaziridinone and other di-tert-alkylaziridinones with cyanamides produces an imidazolidinone (3 or 6) bearing the tert-alkyl substituents at positions 1 and 5 only, by selective cleavage of the acyl-nitrogen bond. Treatment of the product from the unsubstituted cyanamide...
Saved in:
Main Authors: | M. M., Yusoff, Talaty, Erach R., S. Asmah, Ismail, Gomez, Jaime A., Keller, Charles E., Younger, Jean M. |
---|---|
Format: | Article |
Published: |
Georg Thieme Verlag
1997
|
Subjects: | |
Online Access: | http://umpir.ump.edu.my/id/eprint/4784/ http://dx.doi.org/10.1055/s-1997-3256 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Ring-expansion of an Aziridinone to a Hexahydrotriazine Through the Agency of a Novel Rearrangement
by: M. M., Yusoff, et al.
Published: (1996) -
Regioselectivity in nucleophilic ring-opening of aziridinones
by: M. M., Yusoff, et al.
Published: (1998) -
Synthesis and characterization of amino acid-derived hydantoins
by: Chin, Ee-Zhen, et al.
Published: (2021) -
Synthesis and biological evaluation of hydantoin derivatives as potent antiplasmodial agents
by: Chin, Ee-Zhen, et al.
Published: (2024) -
Synthesis and X-ray Analysis of (RS)-N-tert-butyl-2-anilino- 3,3-dimethylbutanamide
by: M. M., Yusoff, et al.
Published: (1997)