In view of the inoreaeing current intereat in qnthetio approaahee to the diterpenoid alkaloids' and to ths tetraonyolio diterpenes2, we should like to present some of our own preliminary results in this field. Our overdll aim is the deVelOpmbnt of a general approach to the mirror image forms of alka
An approach to the total synthesis of ribasine alkaloids
β Scribed by Ricardo Alonso; Luis Castedo; Domingo Dominguez
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 227 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The first total synthesis of A-and D-ring unsubstituted ribasine
π SIMILAR VOLUMES
Macrocylization via formation of aryl-alkyl ether bond was a key step in a model synthesis of 14-membered cyclopeptide alkaloids. A new chemoenzymadc synthesis of chiral 2amino-l-arylethanol was developed in the course of this study
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