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


Autoria(s): Rao, Rama AV; Reddy, Ashok K; Srinivas, NR; Gurjar, MK; Padmaja, N; Ramakumar, S; Viswamitra, MA; Swapna, GVT; Jagannadh, B; Kunwar, AC
Data(s)

07/06/1993

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