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SM ISO690:2012 KULCIŢKI, Veaceslav, CARA, Marina, BOURDELAIS, Andrea, SCHUSTER, Tomas, BADEN, Daniel. Synthesys of a functionalized furan fragment through bromination-cyclization of a conjugated diene. In: Chemistry Journal of Moldova, 2010, nr. 1(5), pp. 118-120. ISSN 1857-1727. |
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Chemistry Journal of Moldova | ||||||
Numărul 1(5) / 2010 / ISSN 1857-1727 /ISSNe 2345-1688 | ||||||
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Pag. 118-120 | ||||||
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This paper describes the use of a terpenic model substrate to conjugate 1,4-additions of N-bromosuccinimide (NBS) to a diene system possessing a suitable oxygen functionality. The reaction leads to functionalized tetrahydrofuran derivatives, which can be developed further into different synthetic targets, such as polyethers, which are known to possess diverse biological activity.
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Cuvinte-cheie terpenoids, furans, NBS, conjugate addition |
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Dublin Core Export
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