Recently new reqlospecific syntheses of both aminotropones (via hydride
Regiospecific synthesis of 1,3-diazaazulenes
β Scribed by Renzo Cabrino; Bruno Ricciarelli; Francesco Pietra
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 200 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Recently it has become possible to functionalize the cycloheptatrienone nucleus specifically at either C(2) or C(7).' Briefly, cycloheptatrienones carrying a displaceable group at C(2) react with nucleophiles by competitive paths a and & (Scheme).' Path a is favoured by both mesomerically electron
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Fluorescence quanu~m yields and fluorescence lifetimes of I.5diazaazulene were measured in cyclohexane. benzene and ethanol. The fluoresccncr quannm~ yield (O.OOZ4 in cyclohexanc, L 1 wd the fluorescence IifeCme (0.80 ns in cyclohexane) are only slightly affected by the solvents. A rather !arge quam
From mixed crystal polarization studies, the lolvesr energy absorption system of 1,3-diazaazulene (cyclohcptimidrrzole) at 4500 A is assigned 3s ' Br (Rn\*j + 'At. The Bt symmetry and oscillator strength of the 4500 A state, together with polarization data on other azaazulenes, clearly indicate a co
## Abstract The magnetic circular dichroism and UV. spectra of 2βmethylβ1, 3βdiazaazulene (**2**) have been measured. The UV. spectrum is interpreted by making use of CNDO/S MO CI calculations. Our assignment of the first and second absorption band coincides with one of the corresponding bands of 1
Condensation of colchicinoids and isocolchicinoids with amidines in dry benzene affords regioselectively 1,3-diazaazulene derivatives: ipso-substitution-condensation products (e,g. 7) are best obtained from cycloheptatrienone-ring deactivated substrates (e.g. 4), whereas isomeric tele-subsfitution-c