## Abstract Lβ[4β^13^C]Lysine (**2**) was synthesized from sodium [2β^13^C]acetate (**3**) and Dellaria's oxazinone **1** as a chiral glycine equivalent. Wittig reaction of the glycinal **7** and ^13^Cβlabeled phosphonium ylide **5**, prepared from sodium [2β^13^C]acetate (**3**), gave the __Ξ±__, _
An Efficient Asymmetric Synthesis of Fmoc-L-cyclopentylglycine via Diastereoselective Alkylation of a Glycine Enolate Equivalent.
β Scribed by Satendra Singh; Michael W. Pennington
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 111 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
## 1997 aminocarboxylic acids aminocarboxylic acids (hydrazinocarboxylic acids) and esters (acyclic compounds) P 0270 ## 40 -103 Highly Diastereoselective Aza-Aldol Reactions of a Chiral Ni(II) Complex of Glycine with Imines. An Efficient Asymmetric Approach to 3-Perfluoroalkyl-2,3-diamino Acids.
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