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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 34, 2004 - Issue 6
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Original Articles

An Improved Preparation of N2‐tert‐Butoxycarbonyl‐ and N2‐Benzyloxy‐carbonyl‐(S)‐2,4‐diaminobutanoic Acids

Ryszard Andruszkiewicz Department of Pharmaceutical Technology and Biochemistry, Gdańsk University of Technology, 80‐952, Gdańsk, PolandCorrespondence[email protected]
&
Dorota Rożkiewicz Department of Pharmaceutical Technology and Biochemistry, Gdańsk University of Technology, 80‐952, Gdańsk, Poland
Pages 1049-1056 | Received 14 Aug 2003, Published online: 21 Aug 2006

Citations (8)

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Read on this site (1)

Ryszard Andruszkiewicz, Ewa Gronek & Jolanta Hałuszczak. (2008) Facile Synthetic Route to Selectively Protected Spermidine Homologues. Synthetic Communications 38:6, pages 905-913.
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Articles from other publishers (7)

Akira Yoshimura & Viktor V. Zhdankin. (2016) Advances in Synthetic Applications of Hypervalent Iodine Compounds. Chemical Reviews 116:5, pages 3328-3435.
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Viktor V. Zhdankin. 2013. Hypervalent Iodine Chemistry. Hypervalent Iodine Chemistry 145 336 .
Leman Karadeniz & Stephen T. Astley. (2012) Catalyst functional group cooperativity in the amino acid-catalysed nitroaldol condensation reaction. Research on Chemical Intermediates 39:7, pages 3407-3415.
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Henrik Johansson & Daniel Sejer Pedersen. (2012) Azide- and Alkyne-Derivatised α-Amino Acids. European Journal of Organic Chemistry 2012:23, pages 4267-4281.
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Aleksandra A. Zagulyaeva, Christopher T. Banek, Mekhman S. Yusubov & Viktor V. Zhdankin. (2010) Hofmann Rearrangement of Carboxamides Mediated by Hypervalent Iodine Species Generated in Situ from Iodobenzene and Oxone: Reaction Scope and Limitations. Organic Letters 12:20, pages 4644-4647.
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Swati S. More & Robert Vince. (2009) Inhibition of Glyoxalase I: The First Low-Nanomolar Tight-Binding Inhibitors. Journal of Medicinal Chemistry 52:15, pages 4650-4656.
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Ryszard Andruszkiewicz & Dorota Rozkiewicz. (2004) An Improved Preparation of N 2 ‐tert‐Butoxycarbonyl‐ and N 2 ‐Benzyloxycarbonyl‐(S)‐2,4‐diaminobutanoic Acids. . ChemInform 35:32.
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