The first total synthesis of A-and D-ring unsubstituted ribasine
An approach to the total synthesis of the diterpenoid alkaloids.
β Scribed by A.A. Othman; N.A.J. Rogers
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 213 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
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 alkaloid6 of the atislne (I) and veatchine (II) groups, using podooarplo aoid M a source material. The present oommuuloation desorlbes aome model experiments in the 2,4a-ethanodeoahydronaphthalene clerielr, designed to teat the applicability of our aynthetio scheme to the B/C/D ring system of the atiaine group. la).
b). Cl' d). e)f). 8). h).
π SIMILAR VOLUMES
The Diels Alder reactions of 5-methoxyindenone followed by intramolecular cyclopropanation provide the basis for a new and more efficient approach to the synthesis of the unusual diterpenoid tropone, harringtonolide.
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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