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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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Bibliographic Details
Main Authors: M. M., Yusoff, Talaty, Erach R.
Format: Article
Language:English
Published: Royal Society of Chemistry 1998
Subjects:
Q Science (General)
QD Chemistry
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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spelling my.ump.umpir.47712018-01-22T01:40:49Z 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) http://dx.doi.org/10.1039/A800564H DOI: 10.1039/A800564H
institution Universiti Malaysia Pahang
building UMP Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Pahang
content_source UMP Institutional Repository
url_provider http://umpir.ump.edu.my/
language English
topic Q Science (General)
QD Chemistry
spellingShingle Q Science (General)
QD Chemistry
M. M., Yusoff
Talaty, Erach R.
Regioselectivity in nucleophilic ring-opening of aziridinones
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.
format Article
author M. M., Yusoff
Talaty, Erach R.
author_facet M. M., Yusoff
Talaty, Erach R.
author_sort M. M., Yusoff
title Regioselectivity in nucleophilic ring-opening of aziridinones
title_short 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_sort regioselectivity in nucleophilic ring-opening of aziridinones
publisher Royal Society of Chemistry
publishDate 1998
url 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
_version_ 1643665057368768512
score 13.211869

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