The complete 1H and 13C assignment of two closely related isomeric triterpenoid derivatives (methyl 2a,3b-di-Oacetylolean-12-en-28-oate and methyl 2a,3a-di-O-acetylurs-12-en-28-oate) is described. In addition to 1D NMR methods, 2D shift-correlated NMR techniques (COSY, NOESY, HMBC and HMQC) were use
Structural elucidation and total assignment of the 1H and 13C NMR spectra of new chalcone dimers
β Scribed by Mary Anne M. Bandeira; F. J. de A. Matos; R. Braz-Filho
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 117 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1292
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β¦ Synopsis
Abstract
Conventional 1D NMR methods and 2D shiftβcorrelated NMR experiments (COSY, HMQC, HMBC) were used for the structural elucidation and ^1^H and ^13^C chemical shifts assignments of four new types of chalcone dimers isolated from Myracrodruon urundeuva. Copyright Β© 2003 John Wiley & Sons, Ltd.
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The complete 1 H and 13 C chemical shift assignment of two closely related isomeric triterpenoids, 3Λ,16Λ,20(R),25-tetrahydroxy-2,11,22-trioxocucurbita-5,23(E)-diene and 3Λ,16Λ,20(R)-trihydroxy-25-acetoxy-2,11,22trioxocucurbita-5,23(E)-diene, making use of one-and two-dimensional NMR techniques (HMB