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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 21, 1991 - Issue 2
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Original Articles

A Novel Route to N-Alkylated Derivatives of Aziridine-2-Carboxylic Acid. an Alternative Synthesis of (S,S)-Bz-Azy-Val-OMe

F. Polyak Institute of Organic Synthesis, Latvian Academy of Sciences, Riga, 226006, LatviaUSSR
,
T. Dorofeeva Institute of Organic Synthesis, Latvian Academy of Sciences, Riga, 226006, LatviaUSSR
,
R. Sturkovich Institute of Organic Synthesis, Latvian Academy of Sciences, Riga, 226006, LatviaUSSR
&
Yu. Goldberg Institute of Organic Synthesis, Latvian Academy of Sciences, Riga, 226006, LatviaUSSR
Pages 239-248 | Received 21 Nov 1990, Published online: 23 Sep 2006

Citations (7)

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Read on this site (1)

Ali Sharifi, Roghiyeh Salimi, Mojtaba Mirzaei & M. Saeed Abaee. (2007) Darzens Reaction Promoted by KF/Alumina: A Novel Stereoselective Method for Rapid and Efficient Synthesis of trans‐α,β‐Epoxy Ketones. Synthetic Communications 37:11, pages 1825-1832.
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Articles from other publishers (6)

Jekaterīna Ivanova, Boriss Štrumfs & Raivis Žalubovskis. (2019) Access to NH-aziridine-2-carboxamides through Davidsen acylimidodicarbonate activation. Comptes Rendus Chimie 22:4, pages 283-293.
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Qi Han, Hui-Yin Li, Vittorio Pace, Jose V. Sinisterra & Andrés R. Alcántara. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Vittorio Pace, Jose V. Sinisterra & Andrés R. Alcántara. 2001. Encyclopedia of Reagents for Organic Synthesis. Encyclopedia of Reagents for Organic Synthesis.
Benjamin E. Blass. (2002) KF/Al2O3 Mediated organic synthesis. Tetrahedron 58:46, pages 9301-9320.
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Thomas Hauck, Karlheinz Sünkel & Wolfgang Beck. (1995) Transition metal complexes of l-aziridine-carboxylate. Inorganica Chimica Acta 235:1-2, pages 391-396.
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F. POLYAK, T. DOROFEEVA, R. STURKOVICH & YU. GOLDBERG. (2010) ChemInform Abstract: A Novel Route to N‐Alkylated Derivatives of Aziridine‐2‐carboxylic Acid. An Alternative Synthesis of (S,S)‐Bz‐Azy‐Val‐OMe.. ChemInform 22:48.
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