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1.
Org Biomol Chem ; 21(6): 1303-1315, 2023 Feb 08.
Artículo en Inglés | MEDLINE | ID: mdl-36648089

RESUMEN

An efficient approach to access chiral N-α indole substituted pyrrolidine and piperidine skeletons has been developed through a AgSbF6-catalyzed N-α aza-Friedel-Crafts alkylation of N,O-acetals 6a, 6b, 9, and 11a-11d with indoles. As a result, a series of 2,3-trans N-α indole substituted pyrrolidines 8a-8x and piperidines 10a-10j were prepared in moderate to excellent yields and with excellent diastereoselectivities (dr up to 99 : 1). Moreover, several 2,5-cis-N-α indole substituted pyrrolidine derivatives 12a-12k were synthesized according to this strategy with moderate to good yields and diastereoselectivities (dr up to 99 : 1).

2.
Org Biomol Chem ; 20(11): 2261-2270, 2022 03 16.
Artículo en Inglés | MEDLINE | ID: mdl-35229848

RESUMEN

An efficient approach to access functionalized indole derivatives has been developed through Cu(OTf)2-catalyzed C3 aza-Friedel-Crafts alkylation of substituted indoles 5a-5m, N-methyl-pyrrole with linear N,O-acetals 4a-4l. As a result, a series of C3 amide aza-alkylated indole derivatives 6a-6ag and 7 were synthesized in moderate to excellent yields.


Asunto(s)
Acetales , Indoles , Alquilación , Catálisis , Estructura Molecular , Estereoisomerismo
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