Abstract:
Reaction between lithium enolates derived from t-butyl esters and l6β-acetoxy-17-oxo-androstane derivatives allowed regiospecific introduction of the side-chain only on C-17 of the steroid nucleus. © 1990, Taylor & Francis Group, LLC. All rights reserved.
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Citas:
---------- APA ----------
Dollar, D. & Gros, E.G.
(1990)
. Side-chain introduction in 16 β-acetoxy-17-oxo-androstanes. Synthetic Communications, 20(20), 3115-3124.
http://dx.doi.org/10.1080/00397919008051534---------- CHICAGO ----------
Dollar, D., Gros, E.G.
"Side-chain introduction in 16 β-acetoxy-17-oxo-androstanes"
. Synthetic Communications 20, no. 20
(1990) : 3115-3124.
http://dx.doi.org/10.1080/00397919008051534---------- MLA ----------
Dollar, D., Gros, E.G.
"Side-chain introduction in 16 β-acetoxy-17-oxo-androstanes"
. Synthetic Communications, vol. 20, no. 20, 1990, pp. 3115-3124.
http://dx.doi.org/10.1080/00397919008051534---------- VANCOUVER ----------
Dollar, D., Gros, E.G. Side-chain introduction in 16 β-acetoxy-17-oxo-androstanes. Synth. Commun. 1990;20(20):3115-3124.
http://dx.doi.org/10.1080/00397919008051534