Stereocontrolled synthesis of the C-1 to C-7 fragment of erythronolide A. A model study using the 1,7-dioxaspiro[5.5]undecane system
- 1 December 1984
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 62 (12), 2929-2935
- https://doi.org/10.1139/v84-496
Abstract
Propionate spiroketal was prepared by 2 different methods. This compound was then converted into the substituted spiro[5.5]undecane which contains 5 contiguous chiral centers which are found in the seco acid of erythronolide A [an antibiotic].This publication has 6 references indexed in Scilit:
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