An asymmetric copper-catalyzed addition produces high enantioselectivity in chiral heterocycles, suggesting efficient synthesis strategies.
An asymmetric copper-catalyzed borylative addition protocol enabling the synthesis of a series of chiral (hydro)indoloquinazoline heterocycles with high enantioselectivity (up to 98% ee) and moderate diastereoselectivity is reported here. This catalytic reaction successfully constructs a C2-quaternary stereogenic center within the (hydro)indoloquinazoline framework by employing commercially available diphosphine ligand Xyl-PPhos under mild conditions. The successful scale-up experiments and derivatization studies further demonstrate excellent chiral retention ability.
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Tang et al. (2026) studied this question.
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