The DMAP-catalyzed [4＋2] cycloaddition of α,β-unsaturated carboxylic acids with ketones furnishing α,β-unsaturated δ-lactones in good yields （up to 80%） is described, which is the first example of remote -C（s...The DMAP-catalyzed [4＋2] cycloaddition of α,β-unsaturated carboxylic acids with ketones furnishing α,β-unsaturated δ-lactones in good yields （up to 80%） is described, which is the first example of remote -C（sp^3）-H activation of α,β-unsaturated carboxylic acids facilitated by DMAP, a pyridine-based catalyst.展开更多
基金This work is supported by the National Natural Science Foundation of China （No. 21372074）.
文摘The DMAP-catalyzed [4＋2] cycloaddition of α,β-unsaturated carboxylic acids with ketones furnishing α,β-unsaturated δ-lactones in good yields （up to 80%） is described, which is the first example of remote -C（sp^3）-H activation of α,β-unsaturated carboxylic acids facilitated by DMAP, a pyridine-based catalyst.
