Regioselectivity in nucleophilic ring-opening of aziridinones

The proportions of products derived from competing modes of ring-opening of 1,3-di-tert-butylaziridinone and similar aziridinones by a variety of nitrogen, oxygen, sulfur and halogen nucleophiles do not agree with simple guidelines postulated in the literature for these types of aziridinones.

Bibliographic Details
Main Authors: M. M., Yusoff, Talaty, Erach R.
Format: Article
Language:English
Published: Royal Society of Chemistry 1998
Subjects:
Online Access:http://umpir.ump.edu.my/id/eprint/4771/
http://umpir.ump.edu.my/id/eprint/4771/
http://umpir.ump.edu.my/id/eprint/4771/
http://umpir.ump.edu.my/id/eprint/4771/1/Regioselectivity_in_nucleophilic_ring-opening_of_aziridinones.pdf
Description
Summary:The proportions of products derived from competing modes of ring-opening of 1,3-di-tert-butylaziridinone and similar aziridinones by a variety of nitrogen, oxygen, sulfur and halogen nucleophiles do not agree with simple guidelines postulated in the literature for these types of aziridinones.