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.
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Royal Society of Chemistry
1998
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| Subjects: | |
| Online Access: | http://umpir.ump.edu.my/id/eprint/4771/1/Regioselectivity_in_nucleophilic_ring-opening_of_aziridinones.pdf http://umpir.ump.edu.my/id/eprint/4771/ http://dx.doi.org/10.1039/A800564H |
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| 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. |
|---|