S-Oxides of 2-Arylsubstituted 4,4-Diphenyl-1,3-oxathiolan-5-ones.
نویسندگان
چکیده
منابع مشابه
Theoretical Characterization of Three 2,2-Diphenyl-1,3,2-oxazaborolidin-5-ones: Molecules with Fungicide Activities
In this study, a theoretical characterization for three 2,2-diphenyl-1,3,2oxazaborolidin-5-ones was performed using Density Functional Theory. The analyzed molecules have antifungal activity, making them of particular interest.
متن کاملU . S . Patent Dee . 13 , 1994 Sheet 2 of 7 5 , 372 , 859 fa Q 2
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The title compound, C(23)H(19)PSe(2), has a central five-membered twist C(3)PSe ring conformation. One phenyl ring substituent, attached to an sp(2) carbon, is approximately coplanar with the C(3)PSe ring whilst the other organic substituents, attached to an sp(3)-carbon and a P(V) atom, lie on the same side of the ring.
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The title compound, C16H12N2O, exists in the crystalline state as the 5-imino-3,4-di-phenyl--1H-pyrrol-2-one tautomer. The dihedral angles between the pyrrole and phenyl rings are 35.3 (2) and 55.3 (2)°. In the crystal, inversion dimers linked by pairs of N-H⋯N hydrogen bonds generate a graph-set motif of R 2 (2)(8) via N-H⋯N hydrogen bonds.
متن کاملDiphenyl [(S)-1-phenylpropanamido]phosphate
The title compound, C(21)H(22)NO(3)P, was synthesized from the reaction of (C(6)H(5)O)(2)P(O)(Cl) and S-1-phenyl-propyl-amine (1:2 mole ratio) at 273 K, followed by removal of the S-1-phenyl-propyl-amine hydro-chloride by-product by dissolving in H(2)O. The P atom is located in a distorted tetra-hedral environment. The bond angles at the P atom vary from 99.51 (12) to 116.68 (12)°. The sp(2) ch...
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ژورنال
عنوان ژورنال: Acta Chemica Scandinavica
سال: 1969
ISSN: 0904-213X
DOI: 10.3891/acta.chem.scand.23-0489