Chiral polyhydroxylated tetrahydrothiophene derivatives: novel synthesis and structural elucidation by X-ray crystallography, NMR spectroscopy and molecular mechanics calculations
Data(s) |
07/06/1993
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Resumo |
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. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/35363/1/Poly.pdf Rao, Rama AV and Reddy, Ashok K and Srinivas, NR and Gurjar, MK and Padmaja, N and Ramakumar, S and Viswamitra, MA and Swapna, GVT and Jagannadh, B and Kunwar, AC (1993) Chiral polyhydroxylated tetrahydrothiophene derivatives: novel synthesis and structural elucidation by X-ray crystallography, NMR spectroscopy and molecular mechanics calculations. In: Perkin Transactions 1 (11). pp. 1255-1259. |
Publicador |
Royal Society of Chemistry |
Relação |
http://pubs.rsc.org/en/Content/ArticleLanding/1993/P1/p19930001255 http://eprints.iisc.ernet.in/35363/ |
Palavras-Chave | #Physics |
Tipo |
Journal Article PeerReviewed |