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Beilstein J. Org. Chem. 2011, 7, 1064–1069, doi:10.3762/bjoc.7.122
Graphical Abstract
Scheme 1: Halogen–lithium exchange of p-bromoanisole followed by reaction with methanol.
Figure 1: Flow microreactor system for halogen–lithium exchange of aryl halide followed by reaction with meth...
Figure 2: Effects of the temperature (T) and the residence time in R1 (tR1) on the yield of anisole in the Br...
Scheme 2: Halogen-lithium exchange of p-bromoanisole followed by oxidative homocoupling with FeCl3.
Figure 3: Integrated flow microreactor system for oxidative homocoupling reaction of aryllithium with FeCl3. ...
Figure 4: Effects of the temperature (T) and the residence time in R2 (tR2) on the yield of 4,4'-dimethoxybip...
Beilstein J. Org. Chem. 2009, 5, No. 16, doi:10.3762/bjoc.5.16
Scheme 1: Sequential introduction of two electrophiles onto dibromobiaryls using Br-Li exchange reactions.
Scheme 2: Br-Li exchange reaction of 2,2′-dibromobiphenyl (1) with n-BuLi using a conventional macrobatch rea...
Figure 1: Microflow system for Br-Li exchange reaction of 2,2′-dibromobiphenyl (1). T-shaped micromixer: M1 (...
Figure 2: Effect of temperature and residence time in Br-Li exchange reaction of 2,2′-dibromobiphenyl (1) usi...
Figure 3: A microflow system for sequential introduction of two electrophiles. T-shaped micromixer: M1 (ø = 2...
Scheme 3: Br-Li exchange reaction of 4,4′-dibromobiphenyl (17) with n-BuLi using a conventional macrobatch re...
Figure 4: Microflow system for Br-Li exchange reaction of 4,4′-dibromobiphenyl (17). T-shaped micromixer: M1 ...
Figure 5: Effect of temperature and residence time in Br-Li exchange reaction of 4,4′-dibromobiphenyl (17) us...