Intramolecular Aldol Condensation Route to 14α,17α-Propanoestradiols and 14α,17α-Ethano-17a-homoestradiols

James R. Bull、L. M. STEER、Krzysztof Jaworski

1994SynlettBiochemistry, Genetics and Molecular Biology被引 2

摘要

All articles of this category 17β-Acetoxy-3-methoxy-20-oxo-19-nor-17α-pregna-1,3, 5(10)-triene-14-carbaldehyde undergoes intramolecular aldol condensation to give 14α,17α-bridged intermediates which are converted into 14α,17α-propano and 14α,17α-ethano-17a-homo analogues of estradiol.

引用本文（GB/T 7714）

James R. Bull, L. M. STEER, Krzysztof Jaworski. Intramolecular Aldol Condensation Route to 14α,17α-Propanoestradiols and 14α,17α-Ethano-17a-homoestradiols[J]. Synlett, 1994.

引文网络

参考文献与被引分析加载中…

DOI：https://doi.org/10.1055/s-1994-22979

本站仅收录题录与摘要供学习参考，全文版权归属出版方；如有侵权请联系我们删除。