A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes
A regioselective and trans-diastereoselective method for the preparation of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes based on 2-naphthol Mannich bases as precursors of 1,2-naphthoquinone 1-methides and highly polarized β-(N,N-dimethylamino)styrene was developed. The resulting cycloadducts were transf...
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| التنسيق: | Статья |
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2024
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| الوصول للمادة أونلاين: | https://dspace.ncfu.ru/handle/123456789/29287 |
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ir-123456789-292872024-11-28T13:50:46Z A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes Demidov, O. P. Демидов, О. П. 2-aryl-2,3-dihydro-1H-benzo[f]chromenes Isoflavans 2-naphthol Mannich bases Push-pull styrene o-quinone methides Cope reaction Diels–Alder reaction A regioselective and trans-diastereoselective method for the preparation of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes based on 2-naphthol Mannich bases as precursors of 1,2-naphthoquinone 1-methides and highly polarized β-(N,N-dimethylamino)styrene was developed. The resulting cycloadducts were transformed into cyclic acetals and hemiacetals as well as introduced into the Cope reaction leading to 2-aryl-1H-benzo[f]chromenes. 2024-11-28T13:47:30Z 2024-11-28T13:47:30Z 2023 Статья Korzhenko, KS; Yushkova, AS; Rashchepkina, DA; Demidov, OP; Osipov, DV; Osyanin, VA. A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2023. - 59 (11-12). - рр. 745-751. - DOI: 10.1007/s10593-024-03267-6 https://dspace.ncfu.ru/handle/123456789/29287 en Chemistry of Heterocyclic Compounds application/pdf Springer |
| institution |
СКФУ |
| collection |
Репозиторий |
| language |
English |
| topic |
2-aryl-2,3-dihydro-1H-benzo[f]chromenes Isoflavans 2-naphthol Mannich bases Push-pull styrene o-quinone methides Cope reaction Diels–Alder reaction |
| spellingShingle |
2-aryl-2,3-dihydro-1H-benzo[f]chromenes Isoflavans 2-naphthol Mannich bases Push-pull styrene o-quinone methides Cope reaction Diels–Alder reaction Demidov, O. P. Демидов, О. П. A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes |
| description |
A regioselective and trans-diastereoselective method for the preparation of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes based on 2-naphthol Mannich bases as precursors of 1,2-naphthoquinone 1-methides and highly polarized β-(N,N-dimethylamino)styrene was developed. The resulting cycloadducts were transformed into cyclic acetals and hemiacetals as well as introduced into the Cope reaction leading to 2-aryl-1H-benzo[f]chromenes. |
| format |
Статья |
| author |
Demidov, O. P. Демидов, О. П. |
| author_facet |
Demidov, O. P. Демидов, О. П. |
| author_sort |
Demidov, O. P. |
| title |
A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes |
| title_short |
A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes |
| title_full |
A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes |
| title_fullStr |
A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes |
| title_full_unstemmed |
A [4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1H-benzo[f]chromenes |
| title_sort |
[4+2] cycloaddition of push-pull styrenes to 1,2-naphthoquinone 1-methides: a synthesis of 2-aryl-2,3-dihydro-1h-benzo[f]chromenes |
| publisher |
Springer |
| publishDate |
2024 |
| url |
https://dspace.ncfu.ru/handle/123456789/29287 |
| work_keys_str_mv |
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