Reaction of several resveratrol glycoside derivatives with hypochlorites in various media

Standard

Reaction of several resveratrol glycoside derivatives with hypochlorites in various media. / Rogachev, A. D.; Komarova, N. I.; Pozdeeva, A. V. и др.

в: Chemistry of Natural Compounds, Том 48, № 1, 03.2012, стр. 1-7.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Rogachev, AD, Komarova, NI, Pozdeeva, AV, Korchagina, DV, Vasil'Ev, VG, Salakhutdinov, NF & Tolstikov, GA 2012, 'Reaction of several resveratrol glycoside derivatives with hypochlorites in various media', Chemistry of Natural Compounds, Том. 48, № 1, стр. 1-7. https://doi.org/10.1007/s10600-012-0146-z

APA

Rogachev, A. D., Komarova, N. I., Pozdeeva, A. V., Korchagina, D. V., Vasil'Ev, V. G., Salakhutdinov, N. F., & Tolstikov, G. A. (2012). Reaction of several resveratrol glycoside derivatives with hypochlorites in various media. Chemistry of Natural Compounds, 48(1), 1-7. https://doi.org/10.1007/s10600-012-0146-z

Vancouver

Rogachev AD, Komarova NI, Pozdeeva AV, Korchagina DV, Vasil'Ev VG, Salakhutdinov NF и др. Reaction of several resveratrol glycoside derivatives with hypochlorites in various media. Chemistry of Natural Compounds. 2012 март;48(1):1-7. doi: 10.1007/s10600-012-0146-z

Author

Rogachev, A. D. ; Komarova, N. I. ; Pozdeeva, A. V. и др. / Reaction of several resveratrol glycoside derivatives with hypochlorites in various media. в: Chemistry of Natural Compounds. 2012 ; Том 48, № 1. стр. 1-7.

BibTeX

@article{9153bf07d22a46038bd1a71cd2236f97,

title = "Reaction of several resveratrol glycoside derivatives with hypochlorites in various media",

abstract = "The reactions of pterostilbenoside (trans-3,5-dimethoxystilben-4′-O- β-D-glucoside) and Ar-O-Tr derivatives of resveratroloside (3,5-dihydroxystilben-4′-O-β-D-glucoside) and pinostilbenoside (3-methoxy-5-hydroxystilben-4′-O-β-D-glucoside) with NaOCl and t-BuOCl in the presence of the stable nitroxyl radical TEMPO were studied in various media. It was found that the principal product of pterostilbenoside transformation was its 2,6-dichloroderivative, a part of which was oxidized to form 2,6-dichloropterostilbene glucuronide. Trityl ethers of resveratroloside and pinostilbenoside reacted with the hypochlorites to form mixtures of products.",

keywords = "hypochlorites, oxidation, resveratrol, stilbene glycosides, TEMPO, triphenylmethyl ethers",

author = "Rogachev, {A. D.} and Komarova, {N. I.} and Pozdeeva, {A. V.} and Korchagina, {D. V.} and Vasil'Ev, {V. G.} and Salakhutdinov, {N. F.} and Tolstikov, {G. A.}",

year = "2012",

month = mar,

doi = "10.1007/s10600-012-0146-z",

language = "English",

volume = "48",

pages = "1--7",

journal = "Chemistry of Natural Compounds",

issn = "0009-3130",

publisher = "Springer New York",

number = "1",

}

RIS

TY - JOUR

T1 - Reaction of several resveratrol glycoside derivatives with hypochlorites in various media

AU - Rogachev, A. D.

AU - Komarova, N. I.

AU - Pozdeeva, A. V.

AU - Korchagina, D. V.

AU - Vasil'Ev, V. G.

AU - Salakhutdinov, N. F.

AU - Tolstikov, G. A.

PY - 2012/3

Y1 - 2012/3

N2 - The reactions of pterostilbenoside (trans-3,5-dimethoxystilben-4′-O- β-D-glucoside) and Ar-O-Tr derivatives of resveratroloside (3,5-dihydroxystilben-4′-O-β-D-glucoside) and pinostilbenoside (3-methoxy-5-hydroxystilben-4′-O-β-D-glucoside) with NaOCl and t-BuOCl in the presence of the stable nitroxyl radical TEMPO were studied in various media. It was found that the principal product of pterostilbenoside transformation was its 2,6-dichloroderivative, a part of which was oxidized to form 2,6-dichloropterostilbene glucuronide. Trityl ethers of resveratroloside and pinostilbenoside reacted with the hypochlorites to form mixtures of products.

AB - The reactions of pterostilbenoside (trans-3,5-dimethoxystilben-4′-O- β-D-glucoside) and Ar-O-Tr derivatives of resveratroloside (3,5-dihydroxystilben-4′-O-β-D-glucoside) and pinostilbenoside (3-methoxy-5-hydroxystilben-4′-O-β-D-glucoside) with NaOCl and t-BuOCl in the presence of the stable nitroxyl radical TEMPO were studied in various media. It was found that the principal product of pterostilbenoside transformation was its 2,6-dichloroderivative, a part of which was oxidized to form 2,6-dichloropterostilbene glucuronide. Trityl ethers of resveratroloside and pinostilbenoside reacted with the hypochlorites to form mixtures of products.

KW - hypochlorites

KW - oxidation

KW - resveratrol

KW - stilbene glycosides

KW - TEMPO

KW - triphenylmethyl ethers

UR - http://www.scopus.com/inward/record.url?scp=84858318611&partnerID=8YFLogxK

U2 - 10.1007/s10600-012-0146-z

DO - 10.1007/s10600-012-0146-z

M3 - Article

AN - SCOPUS:84858318611

VL - 48

SP - 1

EP - 7

JO - Chemistry of Natural Compounds

JF - Chemistry of Natural Compounds

SN - 0009-3130

IS - 1

ER -

ID: 26770506