2026-04-17T17:50:08Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/55342021-11-02T12:05:28Zcom_10259_3593com_10259_5086com_10259_2604col_10259_3594
Repositorio Institucional de la Universidad de Burgos
author
Sedano Labrador, Carlos
author
Velasco, Rocío
author
Feberero, Claudia
author
Suarez Pantiga, Samuel
author
Sanz Díez, Roberto
2020-10-29T11:25:06Z
2020-10-29T11:25:06Z
2020-08
1523-7060
http://hdl.handle.net/10259/5534
10.1021/acs.orglett.0c02199
1523-7052
The α-lithiobenzyloxy group, easily generated from aryl benzyl ethers by selective α-lithiation with t-BuLi at low temperature, behaves as a directed metalation group (DMG) providing a direct access to o-lithiophenyl α-lithiobenzyl ethers. This ortho-directing effect is reinforced in substrates bearing an additional methoxy group at the meta position. The generated dianions can be reacted with a selection of electrophiles including carboxylic esters and dihalosilanes or germanes, which afford interesting benzofuran, sila(germa)dihydrobenzofuran, and silachroman derivatives from simple aryl benzyl ethers.
eng
Functionalization
Ethers
Rearrangement
Reaction products
Pharmaceuticals
α-Lithiobenzyloxy as a Directed Metalation Group in ortho-Lithiation Reactions
info:eu-repo/semantics/article
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URL
https://riubu.ubu.es/bitstream/10259/5534/1/Sedano-ol_2020.pdf
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Sedano-ol_2020.pdf
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https://riubu.ubu.es/bitstream/10259/5534/4/Sedano-ol_2020.pdf.txt
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Sedano-ol_2020.pdf.txt