## Abstract The use of ^13^C n.m.r. for structure elucidation of a series of products obtained by reaction of dialkylamines with 1,2βdinitrotetrachlorobenzene has shown that the general problem of nonβadditivity of substituent effects of contiguously substituted benzenes may be overcome, with these
The case for a revised structure for hypophyllanthin - an analysis of the 13C N.M.R. spectra of aryltetralins
β Scribed by R.S. Ward; P. Satyanarayana; L. Ramachandra Row; B.V. Gopala Rao
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 225 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A revised structure for hypophyllanthin is proposed on the basis of its 13 C n.m.r. spectrum. 13 C n.m.r. spectra also support the previously proposed structure for nirtetralin and assist in the structural elucidation of a new aryltetralin lignan. Considerable controversy surrounds the structures of the lignans from Phyllanthus niruri.1-6 Thus, while Stevenson has recently proposed a revised structure for phyltetralin! three structures have over the years been suggested for hypophyllanthin. l-3 Examination of the l3 C n.m.r. spectra of nirtetralin and hypophyllanthin confirms structure (L)4 for nirtetralin but suggests that the correct structure for hypophyllanthin is in fact (2)
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## and TON THAT THANG (Equipe de recherche No 195, CNRS