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1.
Nat Prod Commun ; 10(7): 1159-61, 2015 Jul.
Article in English | MEDLINE | ID: mdl-26410999

ABSTRACT

In a continued search for novel diterpenoid glycosides, we recently isolated and characterized a Rebaudioside M derivative with a hydroxyl group at position 15 in the central diterpene core from an extract of Stevia rebaudiana Bertoni. Here we report the complete structure elucidation of 15α-hydroxy-Rebaudioside M (2) on the basis of NMR (1H, 13C, COSY, HSQC-DEPT, HMBC, 1D TOCSY, NOESY) and mass spectral data. Steviol glycoside with a hydroxyl group at C-15 in the central diterpene core has not been previously reported.


Subject(s)
Stevia/chemistry , Diterpenes/chemistry , Diterpenes/isolation & purification , Glycosides/chemistry , Glycosides/isolation & purification
2.
Molecules ; 19(11): 17345-55, 2014 Oct 28.
Article in English | MEDLINE | ID: mdl-25353385

ABSTRACT

To supply the increasing demand of natural high potency sweeteners to reduce the calories in food and beverages, we have looked to steviol glycosides. In this work we report the bioconversion of rebaudioside A to rebaudioside I using a glucosyltransferase enzyme. This bioconversion reaction adds one sugar unit with a 1→3 linkage. We utilized 1D and 2D NMR spectroscopy (1H, 13C, COSY, HSQC-DEPT, HMBC, 1D TOCSY and NOESY) and mass spectral data to fully characterize rebaudioside I.


Subject(s)
Diterpenes, Kaurane/metabolism , Beverages , Food , Glucosides/metabolism , Glucosyltransferases/metabolism , Magnetic Resonance Spectroscopy/methods , Mass Spectrometry/methods , Sweetening Agents/metabolism
3.
Biomolecules ; 4(2): 374-89, 2014 Mar 31.
Article in English | MEDLINE | ID: mdl-24970220

ABSTRACT

A minor product, rebaudioside M2 (2), from the bioconversion reaction of rebaudioside A (4) to rebaudioside D (3), was isolated and the complete structure of the novel steviol glycoside was determined. Rebaudioside M2 (2) is considered an isomer of rebaudioside M (1) and contains a relatively rare 1→6 sugar linkage. It was isolated and characterized with NMR (1H, 13C, COSY, HSQC-DEPT, HMBC, 1D-TOCSY, and NOESY) and mass spectral data. Additionally, we emphasize the importance of 1D and 2D NMR techniques when identifying complex steviol glycosides. Numerous NMR spectroscopy studies of rebaudioside M (1), rebaudioside D (3), and mixture of 1 and 3 led to the discovery that SG17 which was previously reported in literature, is a mixture of rebaudioside D (3), rebaudioside M (1), and possibly other related steviol glycosides.


Subject(s)
Diterpenes, Kaurane/chemistry , Diterpenes, Kaurane/isolation & purification , Diterpenes, Kaurane/metabolism , Stevia/chemistry , Trisaccharides/chemistry , Trisaccharides/isolation & purification , Biotransformation , Isomerism , Magnetic Resonance Spectroscopy , Species Specificity , Trisaccharides/metabolism
4.
Inorg Chem ; 47(24): 11452-4, 2008 Dec 15.
Article in English | MEDLINE | ID: mdl-18998626

ABSTRACT

Arylethynylchromium(III) complexes of the form trans-[Cr(cyclam)(CCC(6)H(4)R)(2)]OTf (where cyclam = 1,4,8,11-tetraazacyclotetradecane, R = H, CH(3), or CF(3) in the para position, and OTf = trifluoromethanesulfonate) have been prepared and characterized by IR spectroscopy and X-ray diffraction. The complexes are emissive with excited-state lifetimes in a deoxygenated fluid solution between 200 and 300 micros.

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