Versatile and highly efficient synthetic routes leading to optically active cyclobutanones, g-amino acids and d-amino alcohols are described. These compounds are relevant synthetic precursors to enantiopure cyclobutane carbocyclic nucleosides and oligopeptides. (-)-(S)-Verbenone is the chiral starti
Synthesis of a precursor of cyclobutane carbocyclic nucleosides from α-pinene
✍ Scribed by Franco Fernández; Carmen López; Antonio R. Hergueta
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 364 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4020
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📜 SIMILAR VOLUMES
Several tiff(: compounds have been synthesized in good overall yields through highly stereoselective Wittig-l-lomer condensations of suitable phosphonates with enantiopure aldehydes easily obtained from a-pinene as chiral precursor. These products, presenting two asymmetric carbons, two or four proc
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