Ethyl Isocyanoacetate as a Useful Glycine Equivalent
Autor: | Somnath Halder, Sambasivarao Kotha |
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Rok vydání: | 2010 |
Předmět: | |
Zdroj: | Synlett. 2010:337-354 |
ISSN: | 1437-2096 0936-5214 |
DOI: | 10.1055/s-0029-1219149 |
Popis: | In this account, we describe a useful synthetic approach to constructdiverse constrained α,α-dialkylated amino acidderivatives using ethyl isocyanoacetate as a glycine equivalent.Various unusual amino acid derivatives, such as cyclophane-, benzocyclo-butene-,and diene-containing systems, are reported here. 1 Introduction 2 Traditional Methods for the Synthesis of Cyclic α-Amino AcidDerivatives 2.1 Bucherer-Berg Method 2.2 Strecker Method 2.3 Schmidt Rearrangement Method 3 Glycine Equivalents 4 Preparation of Isocyanides 5 Preparation of Ethyl Isocyanoacetate 6 Synthesis of Cyclic Amino Acid Derivatives Using Various CarbonElectrophiles 7 Synthesis of Unusual Cyclophane-Based α-Amino Acid Derivatives 8 Synthesis of Bis-Armed Amino Acid Derivatives 9 Synthesis and Applications of Acyclic and Alicyclic Amino AcidDerivatives 10 Conclusion |
Databáze: | OpenAIRE |
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