N-Acyl-α-triphenylphosphonioglycinates in the Synthesis of α,β-Dehydro-α-amino Acid Derivatives
✍ Scribed by Roman Mazurkiewicz; Anna Kuznik; Miroslawa Grymel; Nikodem Kuznik
- Publisher
- Springer Vienna
- Year
- 2004
- Tongue
- English
- Weight
- 130 KB
- Volume
- 135
- Category
- Article
- ISSN
- 0026-9247
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📜 SIMILAR VOLUMES
The two enantiomers of the title dehydroamino acids (DHAAs) have been synthesized through respective Wadsworth-Emmons condensations of a suitable phosphonate with enantiomeric cyclobutyl aldehydes. These compounds, in turn, were prepared by selective manipulation of the functional groups starting fr
In previous papers, l-3 we reported the synthesis of a,S-unsaturated N-acyla-amino acid ester (1) by the condensation of ethyl a-oxocarboxylate with amide or by the treatment of N-acetoxy-N-acyl-a-amino acid ester with Et3N. Up to date,
## Abstract The diagnostic values of the following three spectral criteria for the configuration of __N__‐acyl‐α,β‐dehydro‐α‐amino acid esters were examined: (i) the proton at the β‐position at the double bond of a __Z__‐isomer is shielded if compared with the respective __E__‐isomer $(\delta\_{\be