ArticleRSC advances2025
Photochemical [2 + 2] cycloadditions of naphthalene acrylic acids: templated and untemplated photoreactivity, selective homo/heterodimerizations, and conformational analysis.
Article in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Authors and funding
6 authors.
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Abstract
Selective homo- and heterodimerization reactions of naphthalene acrylic acids have been achieved in a diastereocontrolled manner with the use of 1,8-dihydroxynaphthalene as a covalent template in photochemical [2 + 2] cycloadditions. When the reactions were run in solution, cycloaddition products were obtained in good yields (64-88%), which were subsequently detached from the template
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