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2015-01-01
Shao, Wenjie, Clive, Derrick L. J.
A new family of routes to substituted phenols has been developed. 2-Bromo-3- methoxycyclohex-2-en-1-ones are readily deprotonated at C-6 and the resulting anions react smoothly with a variety of electrophiles; treatment with DBU in PhMe at room temperature then results in efficient aromatization...
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Synthesis of Substituted Resorcinol Monomethyl Ethers from 2-Bromo-3-methoxycyclohex-2-en-1-ones
Download2015-01-01
Shao, Wenjie, Clive, Derrick L. J.
2-Bromo-3-methoxycyclohex-2-en-1-ones are readily alkylated at C-6 with reactive halides, and then treatment with DBU (2 equiv) in PhMe at room temperature results in smooth loss of bromide and aromatization to resorcinol (monomethyl ethers of defined substitution pattern.
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