New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione

A new allyl derivative of curcumin containing three allyl groups (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione was synthesized by the reaction of curcumin with the excess of allyl bromide in the presence of K<sub>2</sub&...

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Main Authors: Anna A. Druzina, Olga B. Zhidkova, Sergey A. Anufriev, Ekaterina V. Dubasova, Ivan V. Ananyev, Samya Banerjee, Igor B. Sivaev, Vladimir I. Bregadze
Format: Article
Language:English
Published: MDPI AG 2024-10-01
Series:Molbank
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Online Access:https://www.mdpi.com/1422-8599/2024/4/M1905
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author Anna A. Druzina
Olga B. Zhidkova
Sergey A. Anufriev
Ekaterina V. Dubasova
Ivan V. Ananyev
Samya Banerjee
Igor B. Sivaev
Vladimir I. Bregadze
author_facet Anna A. Druzina
Olga B. Zhidkova
Sergey A. Anufriev
Ekaterina V. Dubasova
Ivan V. Ananyev
Samya Banerjee
Igor B. Sivaev
Vladimir I. Bregadze
author_sort Anna A. Druzina
collection DOAJ
description A new allyl derivative of curcumin containing three allyl groups (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione was synthesized by the reaction of curcumin with the excess of allyl bromide in the presence of K<sub>2</sub>CO<sub>3</sub> in acetone under reflux. The triple-allylated curcumin was characterized by <sup>1</sup>H and <sup>13</sup>C-NMR spectroscopy and single-crystal X-ray diffraction analysis.
format Article
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spelling doaj-art-087ca5d4efe3434db935bd8e890a0eb22025-08-20T02:01:15ZengMDPI AGMolbank1422-85992024-10-0120244M190510.3390/M1905New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dioneAnna A. Druzina0Olga B. Zhidkova1Sergey A. Anufriev2Ekaterina V. Dubasova3Ivan V. Ananyev4Samya Banerjee5Igor B. Sivaev6Vladimir I. Bregadze7A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilov Str., 119991 Moscow, RussiaA.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilov Str., 119991 Moscow, RussiaA.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilov Str., 119991 Moscow, RussiaN.S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, 31 Leninsky Avenue, 119991 Moscow, RussiaA.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilov Str., 119991 Moscow, RussiaDepartment of Chemistry, Indian Institute of Technology (BHU), Varanasi 221005, UP, IndiaA.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilov Str., 119991 Moscow, RussiaA.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 Vavilov Str., 119991 Moscow, RussiaA new allyl derivative of curcumin containing three allyl groups (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione was synthesized by the reaction of curcumin with the excess of allyl bromide in the presence of K<sub>2</sub>CO<sub>3</sub> in acetone under reflux. The triple-allylated curcumin was characterized by <sup>1</sup>H and <sup>13</sup>C-NMR spectroscopy and single-crystal X-ray diffraction analysis.https://www.mdpi.com/1422-8599/2024/4/M1905curcuminallyl derivativesynthesisNMR spectrasingle-crystal X-ray diffraction
spellingShingle Anna A. Druzina
Olga B. Zhidkova
Sergey A. Anufriev
Ekaterina V. Dubasova
Ivan V. Ananyev
Samya Banerjee
Igor B. Sivaev
Vladimir I. Bregadze
New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione
Molbank
curcumin
allyl derivative
synthesis
NMR spectra
single-crystal X-ray diffraction
title New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione
title_full New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione
title_fullStr New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione
title_full_unstemmed New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione
title_short New Allyl Derivative of Curcumin: Synthesis and Crystal Structure of (1<i>E</i>,6<i>E</i>)-4-allyl-1,7-bis(4′-allyloxy-3′-methoxyphenyl)hepta-1,6-diene-3,5-dione
title_sort new allyl derivative of curcumin synthesis and crystal structure of 1 i e i 6 i e i 4 allyl 1 7 bis 4 allyloxy 3 methoxyphenyl hepta 1 6 diene 3 5 dione
topic curcumin
allyl derivative
synthesis
NMR spectra
single-crystal X-ray diffraction
url https://www.mdpi.com/1422-8599/2024/4/M1905
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