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A stereoselective synthese of the C-15 to C-20 segment of rifamycin-S

✍ 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

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✦ Synopsis


A convenient method has been described


πŸ“œ SIMILAR VOLUMES


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## Abstract Chain extension of an aldehyde by two β€œpropionate” units has been attained by stereoselective allylboration with the chiral 1‐methylbutenyl boronate 3 to give, e.g., the homoallylic alcohol 6, followed by a regioselective hydroboration/carbonylation procedure to give, e.g., the epimeric

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✍ E.J. Corey; Tapio Hase πŸ“‚ Article πŸ“… 1979 πŸ› Elsevier Science 🌐 French βš– 235 KB

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