Use of .beta.-sulfonyl vinyl ketones as equivalents to vinyl ketones in the Robinson annelation. Convergent, highly stereoselective preparation of a hydrindanol related to vitamin D from 2-methylcyclopent-2-enone and lithiated (E)-but-2-enyldiphenylphosphine oxide
- 1 October 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (21) , 5162-5170
- https://doi.org/10.1021/jo00282a038
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Stereoselective total synthesis of testosterone and androsterone viaA/B-ring construction of the steroidal ring system by intramolecular Diels–Alder reactionJournal of the Chemical Society, Perkin Transactions 1, 1986
- New synthesis of two optically active steroid CD ring synthons by microbial asymmetric reductionTetrahedron, 1985
- Reactions of 3-(phenylthio)-3-buten-2-one with cycloalkanones. A new approach to fused phenolsThe Journal of Organic Chemistry, 1982
- Total synthesis of optically active (−)17β-hydroxy-Δ9(10)-desA-androsten-5-oneTetrahedron, 1968