## Abstract A stereoselective synthesis of __threo__‐γ‐hydroxy‐β‐l‐lysine lactone is reported. The __threo__‐amino alcohol functionality is introduced by iodine‐mediated cyclocarbamation of the electron poor allylamine 6. The D‐phenylalanine was used as starting material as synthetic equivalent to
ChemInform Abstract: A Concise and Stereoselective Synthesis of threo-γ-Hydroxy-L-. beta.-lysine Lactone.
✍ Scribed by D. MISITI; G. ZAPPIA; G. DELLE MONACHE
- Book ID
- 112037452
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
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