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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Format: | Article |
Language: | English |
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Royal Society of Chemistry
1998
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Online Access: | http://umpir.ump.edu.my/id/eprint/4771/1/Regioselectivity_in_nucleophilic_ring-opening_of_aziridinones.pdf |
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author | M. M., Yusoff Talaty, Erach R. |
author_facet | M. M., Yusoff Talaty, Erach R. |
author_sort | M. M., Yusoff |
collection | UMP |
description | 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. |
first_indexed | 2024-03-06T11:43:21Z |
format | Article |
id | UMPir4771 |
institution | Universiti Malaysia Pahang |
language | English |
last_indexed | 2024-03-06T11:43:21Z |
publishDate | 1998 |
publisher | Royal Society of Chemistry |
record_format | dspace |
spelling | UMPir47712018-01-22T01:40:49Z http://umpir.ump.edu.my/id/eprint/4771/ Regioselectivity in nucleophilic ring-opening of aziridinones M. M., Yusoff Talaty, Erach R. Q Science (General) QD Chemistry 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. Royal Society of Chemistry 1998 Article PeerReviewed application/pdf en http://umpir.ump.edu.my/id/eprint/4771/1/Regioselectivity_in_nucleophilic_ring-opening_of_aziridinones.pdf M. M., Yusoff and Talaty, Erach R. (1998) Regioselectivity in nucleophilic ring-opening of aziridinones. Chemical Communications (9). 985-986 . ISSN 1359-7345 (print), 1364-548X (online). (Published) http://dx.doi.org/10.1039/A800564H DOI: 10.1039/A800564H |
spellingShingle | Q Science (General) QD Chemistry M. M., Yusoff Talaty, Erach R. Regioselectivity in nucleophilic ring-opening of aziridinones |
title | Regioselectivity in nucleophilic ring-opening of aziridinones |
title_full | Regioselectivity in nucleophilic ring-opening of aziridinones |
title_fullStr | Regioselectivity in nucleophilic ring-opening of aziridinones |
title_full_unstemmed | Regioselectivity in nucleophilic ring-opening of aziridinones |
title_short | Regioselectivity in nucleophilic ring-opening of aziridinones |
title_sort | regioselectivity in nucleophilic ring opening of aziridinones |
topic | Q Science (General) QD Chemistry |
url | http://umpir.ump.edu.my/id/eprint/4771/1/Regioselectivity_in_nucleophilic_ring-opening_of_aziridinones.pdf |
work_keys_str_mv | AT mmyusoff regioselectivityinnucleophilicringopeningofaziridinones AT talatyerachr regioselectivityinnucleophilicringopeningofaziridinones |