Synthesis of γ,δ-Aziridino α-Amino Acid Derivatives and their Stereoselective Ring Transformation to 2-(Aminomethyl)-1-aminocyclopropanecarboxylic Acid Derivatives
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| Yazarlar | Nural, Yahya |
| Kurum Dışı Yazarlar | De Brabandere, Stijn Mangelinckx, Sven Kadam, Santosh T. Augustyns, Koen Van der Veken, Pieter Tornroos, Karl W. De Kimpe, Norbert |
| Tek Biçim Adres (URI) | https://hdl.handle.net/20.500.14114/8688 |
| Yayın Türü | Makale |
| Yayın Yılı | 2014 |
| DOI Adresi | 10.1002/ejoc.201301030 |
| Yayıncı | WILEY-V C H VERLAG GMBH |
| Dergi Adı | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY |
| Konu Başlıkları | α-Amino Acid 2-(Aminomethyl)-1-aminocyclopropanecarboxylic Acid Derivatives |
| İndekslenen Platformlar | Web of Science |
1-Benzyl-2-(bromomethyl)aziridine was successfully substituted with protected glycine esters to afford alkyl 3-(N-benzylaziridin-2-yl)-2-aminopropanoates, as constrained heterocyclic diamino acid derivatives, in good isolated yields. These new aziridines proved to be excellent building blocks for ring transformation to the corresponding stereochemically defined 2-(aminomethyl)-1-aminocyclopropanecarboxylic acid derivatives, including methyl esters, piperidyl amides, and free carboxylic acids.
Koleksiyonlar
- Fakülteler
- Eczacılık Fakültesi
- Temel Eczacılık Bilimleri Bölümü
- Analitik Kimya Anabilim Dalı
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Eser Adı dc.title |
Synthesis of γ,δ-Aziridino α-Amino Acid Derivatives and their Stereoselective Ring Transformation to 2-(Aminomethyl)-1-aminocyclopropanecarboxylic Acid Derivatives |
|---|---|
|
Yazarlar dc.contributor.author |
Nural, Yahya |
|
Kurum Dışı Yazarlar dc.contributor.other |
De Brabandere, Stijn |
|
Kurum Dışı Yazarlar dc.contributor.other |
Mangelinckx, Sven |
|
Kurum Dışı Yazarlar dc.contributor.other |
Kadam, Santosh T. |
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Kurum Dışı Yazarlar dc.contributor.other |
Augustyns, Koen |
|
Kurum Dışı Yazarlar dc.contributor.other |
Van der Veken, Pieter |
|
Kurum Dışı Yazarlar dc.contributor.other |
Tornroos, Karl W. |
|
Kurum Dışı Yazarlar dc.contributor.other |
De Kimpe, Norbert |
|
Yayıncı dc.publisher |
WILEY-V C H VERLAG GMBH |
|
Yayın Türü dc.type |
Makale |
|
Özet dc.description.abstract |
1-Benzyl-2-(bromomethyl)aziridine was successfully substituted with protected glycine esters to afford alkyl 3-(N-benzylaziridin-2-yl)-2-aminopropanoates, as constrained heterocyclic diamino acid derivatives, in good isolated yields. These new aziridines proved to be excellent building blocks for ring transformation to the corresponding stereochemically defined 2-(aminomethyl)-1-aminocyclopropanecarboxylic acid derivatives, including methyl esters, piperidyl amides, and free carboxylic acids. |
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Kayıt Giriş Tarihi dc.date.accessioned |
2025-12-26 |
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Yayın Yılı dc.date.issued |
2014 |
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Açık Erișim Tarihi dc.date.available |
2099-01-01 |
|
Dil dc.language.iso |
eng |
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Konu Başlıkları dc.subject |
α-Amino Acid |
|
Konu Başlıkları dc.subject |
2-(Aminomethyl)-1-aminocyclopropanecarboxylic Acid Derivatives |
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Atıf İçin Künye dc.identifier.citation |
De Brabandere, S., Mangelinckx, S., Kadam, S. T., Nural, Y., Augustyns, K., Van der Veken, P., ... & De Kimpe, N. (2014). Synthesis of γ, δ‐Aziridino α‐Amino Acid Derivatives and their Stereoselective Ring Transformation to 2‐(Aminomethyl)‐1‐aminocyclopropanecarboxylic Acid Derivatives. European Journal of Organic Chemistry, 2014(6), 1220-1226. |
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ISSN dc.identifier.issn |
1434-193X |
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İlk Sayfa dc.identifier.startpage |
1220 |
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Son Sayfa dc.identifier.endpage |
1226 |
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Makale Numarası dc.identifier.articlenumber |
- |
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Dergi Adı dc.relation.journal |
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY |
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Dergi Sayısı dc.identifier.issue |
6 |
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Dergi Cilt dc.identifier.volume |
2014 |
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Tek Biçim Adres (URI) dc.identifier.uri |
https://doi.org/10.1002/ejoc.201301030 |
|
Tek Biçim Adres (URI) dc.identifier.uri |
https://hdl.handle.net/20.500.14114/8688 |
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DOI Numarası dc.identifier.doi |
10.1002/ejoc.201301030 |
|
İndekslenen Platformlar dc.source.database |
Web of Science |
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