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...

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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/
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http://umpir.ump.edu.my/id/eprint/4784/
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spelling ump-47842018-01-22T01:37:49Z http://umpir.ump.edu.my/id/eprint/4784/ Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones M. M., Yusoff Talaty, Erach R. S. Asmah, Ismail Gomez, Jaime A. Keller, Charles E. Younger, Jean M. Q Science (General) QD Chemistry 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 (3) with HNO 2 furnishes the corresponding hydantoin (5), whereas treatment with alkyl halides and base affords another imidazolidinone (7) Georg Thieme Verlag 1997 Article PeerReviewed M. M., Yusoff and Talaty, Erach R. and S. Asmah, Ismail and Gomez, Jaime A. and Keller, Charles E. and Younger, Jean M. (1997) Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones. Synlett, 6. pp. 683-684. ISSN 0936-5214, ESSN: 1437-2096 http://dx.doi.org/10.1055/s-1997-3256 DOI: 10.1055/s-1997-3256
repository_type Digital Repository
institution_category Local University
institution Universiti Malaysia Pahang
building UMP Institutional Repository
collection Online Access
topic Q Science (General)
QD Chemistry
spellingShingle Q Science (General)
QD Chemistry
M. M., Yusoff
Talaty, Erach R.
S. Asmah, Ismail
Gomez, Jaime A.
Keller, Charles E.
Younger, Jean M.
Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones
description 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 (3) with HNO 2 furnishes the corresponding hydantoin (5), whereas treatment with alkyl halides and base affords another imidazolidinone (7)
format Article
author M. M., Yusoff
Talaty, Erach R.
S. Asmah, Ismail
Gomez, Jaime A.
Keller, Charles E.
Younger, Jean M.
author_facet M. M., Yusoff
Talaty, Erach R.
S. Asmah, Ismail
Gomez, Jaime A.
Keller, Charles E.
Younger, Jean M.
author_sort M. M., Yusoff
title Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones
title_short Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones
title_full Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones
title_fullStr Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones
title_full_unstemmed Preparation of Substituted Imidazolidinones and Hydantoins by Ring-Expansion of Aziridinones
title_sort preparation of substituted imidazolidinones and hydantoins by ring-expansion of aziridinones
publisher Georg Thieme Verlag
publishDate 1997
url http://umpir.ump.edu.my/id/eprint/4784/
http://umpir.ump.edu.my/id/eprint/4784/
http://umpir.ump.edu.my/id/eprint/4784/
first_indexed 2023-09-18T21:59:41Z
last_indexed 2023-09-18T21:59:41Z
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