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Cited by 381

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

NMR Study of the Solution Structure of Curcumin

Payton, Florastina, Sandusky, Peter, Alworth, William L.·2007·Journal of Natural Products

Abstract

Curcumin [1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione] is derived from the rhizomes of Curcuma longa. Although early studies concluded that curcumin exists predominantly as a keto-enol tautomer, 1b, in several recent articles the solution structure of curcumin has been represented as a beta-diketone tautomer, 1a. We have investigated the structure of curcumin in solvents ranging in polarity from CDCl3 to mixtures of DMSO-d6 in water, and in buffered aqueous DMSO-d6 solutions with pH values varying from 3 to 9. The solution structure of curcumin was determined on the basis of NMR techniques, including DEPT, HMQC, HMBC, and COSY. The results of the NMR studies show definitely that curcumin exists in solution as keto-enol tautomers, 1b.

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Crossref · 10.1021/np060263s

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Metadata

Authors
Payton, F., Sandusky, P., & Alworth, W. L.
Venue
Journal of Natural Products
Published
2007-01-19
Volume
70
Issue
2
Pages
143-146
ISSN
  • 0163-3864 (ISSN-L)
  • 1520-6025
OpenAlex
W2020374958
Cited by
381
References
6
FWCI
5.59
Type
journal article
Language
en
Open access
closed

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