Differentiation of keto groups in the Michael adducts of levoglucosenone with cyclohexanone
- Авторлар: Galimova Y.S.1, Tagirov A.R.1, Faizullina L.K.1, Salikhov S.M.1, Valeev F.A.1
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Мекемелер:
- Ufa Institute of Chemistry
- Шығарылым: Том 53, № 3 (2017)
- Беттер: 374-380
- Бөлім: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/215909
- DOI: https://doi.org/10.1134/S1070428017030113
- ID: 215909
Дәйексөз келтіру
Аннотация
The keto group in the carbohydrate residue of diastereoisomeric Michael adducts of levoglucosenone and cyclohexanone is more reactive than that in the cyclohexanone fragment. The adducts have been converted to the corresponding ethylene, trimethylene, and dimethyl ketals, tosylhydrazones, oxiranes, and Wittig methylenation products with complete or high regioselectivity.
Авторлар туралы
Yu. Galimova
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
Ресей, pr. Oktyabrya 71, Ufa, Bashkortostan, 450054
A. Tagirov
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
Ресей, pr. Oktyabrya 71, Ufa, Bashkortostan, 450054
L. Faizullina
Ufa Institute of Chemistry
Хат алмасуға жауапты Автор.
Email: sinvmet@anrb.ru
Ресей, pr. Oktyabrya 71, Ufa, Bashkortostan, 450054
Sh. Salikhov
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
Ресей, pr. Oktyabrya 71, Ufa, Bashkortostan, 450054
F. Valeev
Ufa Institute of Chemistry
Email: sinvmet@anrb.ru
Ресей, pr. Oktyabrya 71, Ufa, Bashkortostan, 450054
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