Enyne Chlorides: Substrates for Copper-Catalyzed Asymmetric Allylic Alkylation
作者:Hailing Li、Alexandre Alexakis
DOI:10.1002/anie.201107129
日期:2012.1.23
A select few: Several prochiral enynechlorides were employed as substrates in the title reaction using Grignard reagents as the alkylation reagents (see scheme; CuTC=copper(I) thiophenecarboxylate). Excellent 1,3 substitution regioselectivities and good to excellent enantioselectivities were obtained. The substrate scope is additionally extended to diene chlorides.
Braude; Jones, Journal of the Chemical Society, 1946, p. 123
作者:Braude、Jones
DOI:——
日期:——
Bohlmann,F. et al., Chemische Berichte, 1964, vol. 97, p. 2118 - 2124
作者:Bohlmann,F. et al.
DOI:——
日期:——
Heilbron; Jones; Sondheimer, Journal of the Chemical Society, 1949, p. 606
作者:Heilbron、Jones、Sondheimer
DOI:——
日期:——
The asymmetric reduction of alkenynols with the lithium aluminium hydride-3-O-benzyl-1,2-O-cyclohexylidene-α-<scp>D</scp>-glucofuration complex and the determination of the absolute configuration of naturally occurring allenes
作者:S. R. Landor、B. J. Miller、J. P. Regan、A. R. Tatchell