Issue 11, 1993

Chiral polyhydroxylated tetrahydrothiophene derivatives: novel synthesis and structural elucidation by X-ray crystallography, NMR spectroscopy and molecular mechanics calculations

Abstract

The dideoxygenation reaction of 1,3;4,6-di-O-alkylidene-2,5-di-S-methylthiocarbonyl-D-mannitol derivatives under Barton-McCombie reaction conditions gave the hexahydrodipyranothiophenes 4 and 7 instead of the expected 2,5-dideoxy products. Structural and conformational information on these novel derivatives has been obtained by NMR spectroscopy, single-crystal X-ray crystallography and molecular mechanics calculations.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1993, 1255-1259

Chiral polyhydroxylated tetrahydrothiophene derivatives: novel synthesis and structural elucidation by X-ray crystallography, NMR spectroscopy and molecular mechanics calculations

A. V. R. Rao, K. A. Reddy, N. R. Srinivas, M. K. Gurjar, N. Padmaja, S. Ramakumar, M. A. Viswamitra, G. V. T. Swapna, B. Jagannadh and A. C. Kunwar, J. Chem. Soc., Perkin Trans. 1, 1993, 1255 DOI: 10.1039/P19930001255

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