Pyrans,their analogs,and related compounds

Reaction of 4, 4-dichloroflavine (I) with sulfurylchloride affords 2, 3, 3, 4, 4-pentachloroflavan (II). Hydrolysis of II gives 2-hydroxy-3, 3-dichloro-4-flavanone (III), while alcoholysis with aqueous alcohols yields 2-alkoxy-3,3-dichloro-4-flavanones (IVa, b). Treatment of III with SOCl₂ gives 2,3,3-trlchloro-4-flavanone (V), which with caustic alkali or sodium ethoxide is converted into o-(1-phenyl-2, 2-dichlorovinyloxy)benzoic acid (VIc) or its ethyl ester (VIb), respectively.For Part XLII, see [7].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1167–1170, September, 1970.     

Calculation of Siegert eigenvalues for molecular systems: results for He(21,3S)+ H

The variational calculation of Siegert eigenvalues has previously been shown to provide reliable positions and widths for atomic resonances. This approach is herein extended to molecular problems, and the first such calculations for a molecular autoionizing system, He(2^1,3S)+H→ He+H⁺+e^?, are reported.