Published August 1986 | Version v1
Journal article

Unusual product of the reaction of 1-phenyl-3-(3,4-dimethoxyphenyl)-3-(2-oxocyclohexyl)-1-propanone with hydrogen sulfide and acids: 2α-phenyl-2,4-ortho-(14,15-dimethoxybenzo)-cis-1-thiadecalin

  • 1. N.G. Chernyshevskii Saratov State Univ., USSR

Description

The reaction of 1-phenyl-3-(3,4-dimethoxyphenyl)-3-(2-oxocyclohexyl)-1-propanone with hydrogen sulfide and acids gives an intramolecular rearrangement product, 2α-phenyl-2,4-ortho-(14,15-dimethoxybenzo)-cis-1-thiadecalin in addition to the usual products of disproportionation of intermediate 2-phenyl-4-(3,4-dimethoxyphenyl)-5,6-tetramethylene-4H-thiopyran, namely, 5,6-tetramethylenethio-pyrilium salts and 2α-phenyl-4α-(3,4-dimethoxyphenyl)-cis-1-thiadecalin. The configurational and conformational assignments for the sulfides, their sulfoxides, and sulfones were made by 13C NMR spectroscopy

Additional details

Publishing Information

Journal Title
Chem. Heterocycl. Compd. (Engl. Transl.)
Journal Volume
22
Journal Issue
2
Series
Chem. Heterocycl. Compd. (Engl. Transl.).
Journal Page Range
155-161
ISSN
0069-3154
CODEN
CHCCA

Optional Information

Notes
Translated from Khim. Geterotsikl. Soedin.; 22: No.2, 199-205(Feb 1986).