Pd(OAc)/Nixantphos or CoI/Nixantphos catalyzed allylic substitutions with weakly acidic C(sp)-H bonds of azaarylmethylamines are described. This method facilitates access to various kinds of heteroaryl rings containing homoallylamines (39 examples, 30-98% yields) with excellent functional group tolerance and diastereoselectivity. Compared with the Pd/Nixantphos complex, the Co/Nixantphos catalysis could obtain the cyclic products with good to excellent diastereoselectivities. Importantly, the CoI/()-Me-Duphos catalyzed reactions exhibit moderate enantioselectivity. Additionally, the scalability of this transformation is successfully demonstrated.
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http://dx.doi.org/10.1021/acs.orglett.4c00551 | DOI Listing |
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