Diastereoselective Synthesis of (Z)‐6‐(2‐Oxo‐1,2‐dihydro‐3H‐indol‐3‐ylidene)‐3,3a,9,9a‐tetrahydroimidazo[4,5‐e]thiazolo[3,2‐b]‐1,2,4‐triazin‐2,7(1H,6H)‐diones Научная публикация
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Journal of Heterocyclic Chemistry
ISSN: 0022-152X , E-ISSN: 1943-5193 |
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| Вых. Данные | Год: 2014, Том: 51, Номер: 4, Страницы: 921-926 Страниц : 6 DOI: 10.1002/jhet.2008 | ||
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Реферат:
Two efficient and diastereoselective procedures for the synthesis of (Z)-6-(2-oxo-1,2-dihydro-3H-indol-3-ylidene)-3,3a,9,9a-tetrahydroimidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazin-2,7(1H,6H)-diones by aldol-crotonic condensation of 1,3-dimethyl-3a,9a-diphenyl-3,3a,9,9a-tetrahydroimidazo[4,5-e]thiazolo[3,2-b]-1,2,4-triazin-2,7(1H,6H)-dione with isatins under acidic or basic catalysis are reported. Isomerization in (Z)-7-(1-allyl-2-oxo-1,2-dihydro-3H-indol-3-ylidene)-1,3-dimethyl-3a,9a-diphenyl-1,3a,4,9a-tetrahydroimidazo[4,5-e]thiazolo[2,3-c]-1,2,4-triazin-2,8(3H,7H)-dione was observed under basic conditions.
Библиографическая ссылка:
Gazieva G.A.
, Shishkova E.A.
, Kulikova L.B.
, Kolotyrkina N.G.
, Sigay N.V.
, Kravchenko A.N.
Diastereoselective Synthesis of (Z)‐6‐(2‐Oxo‐1,2‐dihydro‐3H‐indol‐3‐ylidene)‐3,3a,9,9a‐tetrahydroimidazo[4,5‐e]thiazolo[3,2‐b]‐1,2,4‐triazin‐2,7(1H,6H)‐diones
Journal of Heterocyclic Chemistry. 2014. V.51. N4. P.921-926. DOI: 10.1002/jhet.2008 WOS Scopus OpenAlex
Diastereoselective Synthesis of (Z)‐6‐(2‐Oxo‐1,2‐dihydro‐3H‐indol‐3‐ylidene)‐3,3a,9,9a‐tetrahydroimidazo[4,5‐e]thiazolo[3,2‐b]‐1,2,4‐triazin‐2,7(1H,6H)‐diones
Journal of Heterocyclic Chemistry. 2014. V.51. N4. P.921-926. DOI: 10.1002/jhet.2008 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:000340277200007 |
| ≡ Scopus: | 2-s2.0-84905043962 |
| ≡ OpenAlex: | W2949171536 |