Une Synthèse Aisée De Diméthyl-6',6' Pyrannoisoflavones Angulaires

التفاصيل البيبلوغرافية
العنوان: Une Synthèse Aisée De Diméthyl-6',6' Pyrannoisoflavones Angulaires
المؤلفون: J. Jadot, C. Vilain
المصدر: Bulletin des Sociétés Chimiques Belges. 86:237-240
بيانات النشر: Wiley, 2010.
سنة النشر: 2010
مصطلحات موضوعية: Dimethyl acetal, chemistry.chemical_compound, chemistry, Stereochemistry, Pyridine, Condensation, General Chemistry, Piperidine, Medicinal chemistry
الوصف: 3-hydroxyisovaleraldehyde dimethyl acetal(I) is condensed in the presence of pyridine with 2,4-dihydroxy phenyl benzyl ketones (IIa, b, c, d) to give 2,2-dimethyl-6-phenylacetyl-5-hydroxychromenes (IIIa, b, c, d); these intermediates are directly converted into the corresponding angular 6", 6"-dimethylpyranoisoflavones (IVa, b, c, d) by condensation with ethylorthoformate in the presence of pyridine and piperidine. Compounds IV b and IV d are respectively identical with the natural products Calopogonium Isoflavone A and B wich we have described earlier.
تدمد: 0037-9646
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::14af13f886d63a9c7e082b1a480578e9Test
https://doi.org/10.1002/bscb.19770860310Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........14af13f886d63a9c7e082b1a480578e9
قاعدة البيانات: OpenAIRE