## Synthesis of Enantiomerically Pure Carbocyclic α-L-Isomeric Homonucleosides. -The synthesis of hitherto unknown carbocyclic 2',3'-dideoxyhomonucleosides (X)-(XIII) starting from the known chiral lactone (I) is accomplished. The transformation of the (R)-hydroxy group in derivative (IV) to the
Synthesis of enantiomerically pure carbocyclic α-l-isomeric homonucleosides
✍ Scribed by F. Girard; C. Demaison; M.-G. Lee; L.A. Agrofoglio
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 384 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0040-4020
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✦ Synopsis
Synthesis of hitherto unknown carbocyclic a-L-isomeric homonucleosides (Sa-b, 9a.b) is described. The key intermediate 6 was synthesized from the known compound 1 as a chiral starting material. Construction of the heteroo,clic moiety around the amino group of 6 afforded carbocyclic Or-Lisomeric 2 ',3 '-dideoxyhomonucleosides 8a-b and their 2 ',3 '-didehydro-2 ',3'-dideoxy derivatives 9a-b.
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