2-methyl-6,6-bis(trlfluoromethyl)cyclohex-3-ene-1-carbaldehyde: reactivity and application as a model for the preparation of 16,16,16,17,17,17-hexafluororetinal analogs
New approaches to 16,16,16,17,17,17-hexafluororetinal and analogs, via 2-methyl-6,6-bis(trifluoromethyl)cyclohexanone and 2-methyl-6,6-bis(trifluoromethyl)cyclohex-1-ene-1 -carbaldehyde (7,7,7,8,8,8-hexafluoro-β-cyclocitral) are presented. An efficient synthesis for 2-methyl-6,6-bis(trifluoromethyl)...
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| Дата: | 2008 |
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| Автори: | , , , , , , |
| Формат: | Стаття |
| Мова: | English |
| Опубліковано: |
Інститут органічної хімії НАН України
2008
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| Назва видання: | Журнал органічної та фармацевтичної хімії |
| Онлайн доступ: | http://dspace.nbuv.gov.ua/handle/123456789/42345 |
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| Назва журналу: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| Цитувати: | 2-methyl-6,6-bis(trlfluoromethyl)cyclohex-3-ene-1-carbaldehyde: reactivity and application as a model for the preparation of 16,16,16,17,17,17-hexafluororetinal analogs / S. Boichut, C. Boyer, K. Burger, A. Haas, K. Merz, T. Pages, T. Wallmichrath // Журнал органічної та фармацевтичної хімії. — 2008. — Т. 6, вип. 1(21). — С. 3-12. — Бібліогр.: 30 назв. — англ. |
Репозитарії
Digital Library of Periodicals of National Academy of Sciences of Ukraine| Резюме: | New approaches to 16,16,16,17,17,17-hexafluororetinal and analogs, via 2-methyl-6,6-bis(trifluoromethyl)cyclohexanone and 2-methyl-6,6-bis(trifluoromethyl)cyclohex-1-ene-1 -carbaldehyde (7,7,7,8,8,8-hexafluoro-β-cyclocitral) are presented. An efficient synthesis for 2-methyl-6,6-bis(trifluoromethyl)-cyclohex-3-ene-1-carbaldehyde starting from hexafluoroacetone has been described and used for preparing reactive building blocks. The crystal structures of 6, 15 and 23 have been provided and the influence of the bis(trifluoromethyl)-group on bond lengths and angles have been discussed. |
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