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Nitrogen Bridgehead Compounds. Part 32. Absolute Configuration and Circular Dichroism of 6-Methyl-tetrahydro-4H-pyridopyrimidin-4-ones

DOI: 10.1039/P29830001413

Source and publish data:

Journal of the Chemical Society. Perkin transactions II p. 1413 - 1420 (1983)

Update date:2022-09-26

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Authors:

Hermecz, IstvanHermecz, Istvan

Surjan, Peter R.Surjan, Peter R.

Breining, TiborBreining, Tibor

Simon, KalmanSimon, Kalman

Horvath, GaborHorvath, Gabor

et al.et al.

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Article abstract of DOI:10.1039/P29830001413

From the resolved enantiomers of (1b), whose enantiomeric purities were determined by 1H n.m.r., three types of 6-methyl-tetrahydro-4H-pyrido<1,2-a>pyrimidin-4-one derivatives (1)-(3) were prepared in optically active form.The absolute configuration at the chiral centre C(6) was established on the basis of the anomalous X-ray scattering of the bromine atom of the compound (-)-synthesized from compound (+)-(1b).Analysis of the experimental u.v. and c.d. spectra led to the identification of two different types of chromophoric systems in molecules of the types (1) and (2) on the one hand, and in those of type (3) on the other.The results of CNDO/S calculations for the energies, oscillator strengths, and rotational strengths due to the transitions of simple model molecules with geometries based on X-ray data were in good qualitative agreement with the experimental u.v. and c.d. spectra, and allowed the chiroptical properties of compounds (1)-(3) to be correlated with their known absolute geometries.

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Product name:4H-Pyrido[1,2-a]pyrimidinium, 6,7,8,9-tetrahydro-1,6-dimethyl-4-oxo-, (R)-, methyl sulfate

Cas No:88125-38-6

88125-38-6

R&D Labs maybe for 88125-38-6

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