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Synthesis of N-H vinylaziridines: a comparative study
KTH, Superseded Departments, Chemistry.
2002 (English)In: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 58, no 30, 5979-5982 p.Article in journal (Refereed) Published
Abstract [en]

Vinylaziridines are useful and versatile synthetic intermediates, as the relief of ring-strain provides a driving force for efficient ring-opening or ring-expansion reactions. Furthermore, the vinyl group can be derivatized into interesting functionalities. The ring-closure of vicinal amino alcohols constitutes a straightforward route to aziridines. Several methods exist for this transformation, although many cannot be applied to vinylaziridines due to their acid lability. This comparative study describes the most effective sequences for the formation of N-H vinylaziridines.

Place, publisher, year, edition, pages
2002. Vol. 58, no 30, 5979-5982 p.
Keyword [en]
amino alcohols, vinylaziridines, ring-closure, organocopper reagents, aziridines, rearrangement, acids
Identifiers
URN: urn:nbn:se:kth:diva-21751ISI: 000177028600002OAI: oai:DiVA.org:kth-21751DiVA: diva2:340449
Note
QC 20100525Available from: 2010-08-10 Created: 2010-08-10 Last updated: 2017-12-12Bibliographically approved

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