Synthesis of Functional Dihydro-1,4-benzoxaselenines from Carvacrol Allyl Ether and Selenium Dihalides

Synthesis of Functional Dihydro-1,4-benzoxaselenines from Carvacrol Allyl Ether and Selenium Dihalides

One-step procedures have been developed for the selective synthesis of functionalized 2,3-dihydro-1,4-benzoxaselenines in 90–98% yields by cyclization of carvacrol allyl ether with selenium dihalides. Annulation/acetoxyselenation reaction has been performed for the first time.

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Veröffentlicht in:Russian journal of organic chemistry 2020-12, Vol.56 (12), p.2258-2262
Hauptverfasser: Musalov, M. V., Yakimov, V. A., Potapov, V. A., Amosova, S. V.
Format: Artikel
Sprache:eng
Schlagworte:
Chemical reactions
Chemistry
Chemistry and Materials Science
Organic Chemistry
Selenium
Synthesis
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Zusammenfassung:One-step procedures have been developed for the selective synthesis of functionalized 2,3-dihydro-1,4-benzoxaselenines in 90–98% yields by cyclization of carvacrol allyl ether with selenium dihalides. Annulation/acetoxyselenation reaction has been performed for the first time.
ISSN:1070-4280
1608-3393
DOI:10.1134/S1070428020120350