139599-37-4Relevant academic research and scientific papers
Stereoselective SN2′ alkylation reaction sequence of the γ,δ-epoxy α,β-unsaturated ester system via γ,δ-chlorohydrin intermediates by the use of a R3Al-CuCN reagent
Yoshimura, Fumihiko,Matsui, Atsushi,Hirai, Atsushi,Tanino, Keiji,Miyashita, Masaaki
, p. 5126 - 5129 (2009)
A novel stereoselective SN2′ alkylation reaction sequence of the γ,δ-epoxy α,β-unsaturated ester system has been developed which involves a regioselective substitution reaction with chloride ions at the γ-position and a subsequent SN
Multiple Carbon Bond Formation via the Radical Cyclization of Cycloalkenol Acetals. Application to trans Hydrindan Steroid Precursors
Stork, Gilbert,Franklin, Paul J.
, p. 275 - 284 (2007/10/02)
The cyclization of the α-iodo mixed acetals derived from properly substituted cyclohexanols, a process which has already been shown to permit the stereoselective and regioselective introduction of a different carbon chain at each of the termini of the all
