Abstract
AbstractAn efficient protocol for the preparation of indolo[1,2‐a]quinazolines via palladium‐catalyzed decarboxylative annulation of indols with α‐oxocarboxylic acids has been realized by using primary amine as a directing group (DG). This transformation proceeds smoothly with exclusive regioselectivity and represents an one‐pot Domino synthesis of indo‐lo[1,2‐a]quinazolines from α‐oxocarboxylic acids.magnified image
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