Use of the Mitsunobu reaction in the synthesis of orthogonally protected α,β-diaminopropionic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. α,β-Diamino Acids: Biological Significance and Synthetic Approaches
2. Preparation of 2,3-diaminopropionate from ring opening of aziridine-2-carboxylate
3. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
4. A Short Synthetic Approach to Chiral Serine Azido Derivatives
5. Efficient synthesis of orthogonally protected anti-2,3-diamino acids
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3. Studies on the synthesis of orthogonally protected azalanthionines, and of routes towards β-methyl azalanthionines, by ring opening of N-activated aziridine-2-carboxylates;Tetrahedron;2014-08
4. Synthesis of orthogonally protected 1,2-diaminopropanoic acids by ring-opening of 3-unsubstituted N-activated aziridine 2-carboxylates with para-methoxybenzylamine: a study of the regioselectivity of the reaction;Tetrahedron Letters;2013-11
5. Synthesis of orthogonally protected azalanthionines (lanazanines) by sequential ring-opening of N-substituted aziridine 2-carboxylates;Tetrahedron Letters;2013-05
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