Giles, Robin G. F.; Sargent, Melvyn V.; Sianipar, Hercules published the artcile< Regioselectivity in the reactions of methoxydehydrobenzenes with furans. Part 1. Reactions of 3-methoxydehydrobenzene and 3-(methoxycarbonyl)dehydrobenzene with 2-substituted furans>, Product Details of C7H7BrO2, the main research area is cycloaddition furan methoxydehydrobenzene regiochem; dehydrobenzene methoxy cycloaddition furan regiochem; ring cleavage dihydroepoxynaphthalene; naphthol alkoxy.
The isomer ratios for the cycloadducts obtained for the reaction of 3-methoxydehydrobenzene, generated from 2-amino-6-methoxybenzoic acid by aprotic diazotization, or from 2,3-BrMeOC6H3OSO2C6H4Me-4 by treatment with BuLi, and for the reaction of 3-(methoxycarbonyl)dehydrobenzene, generated from 2,6-(H2N)(MeO2C)C6H3CO2H by aprotic diazotization, with seven 2-substituted furans were obtained. These results are discussed in terms of an asynchronous, concerted, biradicaloid reaction pathway.
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) published new progress about Cycloaddition reaction. 135999-16-5 belongs to class bromides-buliding-blocks, and the molecular formula is C7H7BrO2, Product Details of C7H7BrO2.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary