We thank PD Dr. M. Zehnder and Dr. D. Bur. lnstitut fur Anorganische Chemie der Universitiit Basel, for this measurement.
A stereoselective synthese of the C-15 to C-20 segment of rifamycin-S
β Scribed by A.V.Rama Rao; J.S. Yadav; C.Srinivasa Rao
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 108 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
A convenient method has been described
π SIMILAR VOLUMES
## Abstract Chain extension of an aldehyde by two βpropionateβ units has been attained by stereoselective allylboration with the chiral 1βmethylbutenyl boronate 3 to give, e.g., the homoallylic alcohol 6, followed by a regioselective hydroboration/carbonylation procedure to give, e.g., the epimeric
One interesting possibility for the elaboration of the C(15) to C(29) chain of the antibiotic rifamycin S (l)l is illustrated by the antithetic relationship indicated in Scheme I. In this plan the ry SCHEME I 3 intermediate zwhich corresponds to the C(19) to C(27) chain is disconnected to a bifuncti