Synthesis of Diiodo-Functionalized Benzo[b] furans via Electrophilic Iodocyclization
An electrophilic iodocyclization reaction involving alkynylated 2-iodoanisoles and molecular iodine in the presence of sodium bicarbonate was developed and diiodo-functionalized benzo[b] furans were obtained in yields from 45 to 99%.
| Autores: | , , , , |
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| Formato: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2017 |
| País: | Brasil |
| Recursos: | Universidade Federal de São Paulo (UNIFESP) |
| Repositorio: | Repositório Institucional da UNIFESP |
| Idioma: | inglés |
| OAI Identifier: | oai:repositorio.unifesp.br:11600/57314 |
| Acesso em linha: | http://dx.doi.org/10.21577/0103-5053.20170035 https://repositorio.unifesp.br/handle/11600/57314 |
| Access Level: | acceso abierto |
| Palavra-chave: | electrophilic iodocyclization molecular iodine diiodo-functionalized benzo[b] furans functionalized heteroaromatics diiodinated compounds |
| Resumo: | An electrophilic iodocyclization reaction involving alkynylated 2-iodoanisoles and molecular iodine in the presence of sodium bicarbonate was developed and diiodo-functionalized benzo[b] furans were obtained in yields from 45 to 99%. |
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