Producción Científica Profesorado

Regioselective Synthesis of 3-Indolyl(alkoxy)acetates

Meléndez Rodríguez, Myriam


Suárez-Castillo O. R., Meléndez-Rodríguez M., Cano-Escudero Indira C., De Ita-Gutiérrez Sandra Luz, Sánchez-Zavala M., Morales-Ríos M. S. y Joseph-Nathan P., Regioselective Synthesis of 3-indolyl(alcoxy)acetates Heterocycles, 81, 1169, (2010).ISSN: 0385-5414 DOI: 10.3987/COM-10-11904


The regioselective synthesis of N-carbomethoxy-2-alkoxyindolenines and ?-alkoxyindoles is reported. Bromination of indole 5 with NBS/AIBN/CCl4 gave ?-bromoindole 6 which after treatment with ROH/3Å molecular Sieves afforded (Z-) and (E)-2-alkoxyindolenines 8a-d as the main products, together with minor amounts of ?-alkoxyindoles 9a-d. The reversed regioselectivity was achieved in the absence of molecular Sieves to give ?-alkoxyindoles 9a-d as the main products, while no traces of Z- or E-8a-d were detected.

Producto de Investigación

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