Steroidal trans-hydrindanone 6 was stereoselectively synthesized from lactol 1 in nine steps in 27% overall yield via intramolecular ester enolate alkylation methodology. © 1990.
CITATION STYLE
Deukjoon, K., Sanghee, K., Jae, J. L., & Hak, S. K. (1990). Stereoselective construction of steroidal trans-hydrindanes via intramolecular ester enolate alkylation[1,2]. Tetrahedron Letters, 31(28), 4027–4028. https://doi.org/10.1016/S0040-4039(00)94490-3
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