2 research outputs found
Cooperative Cu/Pd-Catalyzed 1,5-Boroacylation of Cyclopropyl-Substituted Alkylidenecyclopropanes
A Cu/Pd-cocatalyzed
1,5-boroacylation of cyclopropyl-substituted
ACPs with B2pin2 and acid chlorides has been
developed. Using cyclopropyl-substituted ACPs as the starting material,
a broad range of 1,5-boroacylated products with multiple functional
groups was prepared in good yields with excellent regio- and stereoselectively.
Both aromatic and aliphatic acid chlorides were tolerated in this
reaction
Cooperative Cu/Pd-Catalyzed 1,5-Boroacylation of Cyclopropyl-Substituted Alkylidenecyclopropanes
A Cu/Pd-cocatalyzed
1,5-boroacylation of cyclopropyl-substituted
ACPs with B2pin2 and acid chlorides has been
developed. Using cyclopropyl-substituted ACPs as the starting material,
a broad range of 1,5-boroacylated products with multiple functional
groups was prepared in good yields with excellent regio- and stereoselectively.
Both aromatic and aliphatic acid chlorides were tolerated in this
reaction