Furfuryl vinyl ethers in [4+2]-cycloaddition reactions


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Аннотация

For the first time [4+2]-cycloaddition reactions were carried out between furfuryl vinyl ethers and typical dienophiles and heterodienes proceeding in uncatalyzed conditions and resulting in previously unknown heterocyclic systems containing either free vinyloxy groups or furfuryl substituents. With maleic anhydride and maleimide furfuryl vinyl ethers afforded 1-(vinyloxyalkyl)tricyclodec-8-ene-3,5-diones in up to 72% yields, and with N-benzylideneaniline or acrolein the corresponding functionally substituted tetrahydroquinolines (yield up to 65%) or 3,4-dihydropyrans (yield 23–50%) were obtained.

Авторлар туралы

K. Apartsin

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: boris_trofimov@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033

N. Gusarova

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: boris_trofimov@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033

B. Trofimov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Хат алмасуға жауапты Автор.
Email: boris_trofimov@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033

L. Oparina

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: boris_trofimov@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033

O. Vysotskaya

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: boris_trofimov@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033

A. Stepanov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: boris_trofimov@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033

I. Ushakov

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: boris_trofimov@irioch.irk.ru
Ресей, ul. Favorskogo 1, Irkutsk, 664033

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