A Simple Method of Cyclization of the 2'-Hydroxychalcone with Polystyrene-Pyridine Resine under Mild Conditions

Xu Xu Zheng; Jing Jing Xie; Zhong Yi Yin; Jia Jia Jing

doi:10.4028/www.scientific.net/AMR.295-297.1156

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HomeAdvanced Materials ResearchAdvanced Materials Research Vols. 295-297A Simple Method of Cyclization of the...

A Simple Method of Cyclization of the 2'-Hydroxychalcone with Polystyrene-Pyridine Resine under Mild Conditions

Abstract:

The satisfying cyclization of 2’-hydroxy chalcone to flavanone using polystyrene-pyridine resine as catalyst and methanol as solvent under mild conditions is reported here. The method is appropriate for 2’-hydroxy chalcone derivatives with electron group in B-ring.

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Periodical:

Advanced Materials Research (Volumes 295-297)

Pages:

1156-1159

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.295-297.1156

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Online since:

July 2011

Authors:

Xu Xu Zheng, Jing Jing Xie, Zhong Yi Yin, Jia Jia Jing

Keywords:

2’-Hydroxy Chalcone, Flavanone, Polystyrene-Pyridine Resine

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References

[1] D Dauzonne, C Monneret.Synthesis,1997, 11:1305-1308.

Google Scholar

[2] M W Borner, H Hindorf, J H Chandra, et al. Phytochemistry,1990, 29(4):1103-1105.

Google Scholar

[3] M J Salvatore, B K Aurora, A C Graham, et al. J.Nat.Prod.Rep,1998, 61:640-642.

Google Scholar

[4] Hu Li Hong, Tan Zhang Lan, Li Chao. Chemical communications, 2003,(1):12-17. (In Chinese)

Google Scholar

[5] T Narender, K Papi Reddy, Brijesh Kumar. Tetrahedron letters,2008,49(28):4409 -4415.

DOI: 10.1016/j.tetlet.2008.05.020

Google Scholar

[6] Dalip Kumar, Gautam Patel, Braja G.Mishra,etal. Tetrahedron Letters,2008,49(49):6974-6976.

Google Scholar

[7] Yu Shan Xin, Tang Chun Yan, Liu Da ming. Jiangsu Chemical ,1999,27(6):14-16. (In Chinese)

Google Scholar

[8] Yu Shan Xin, Tang Chun Yan,Liu Li Zhong. Natural Science of Hunan Normal University. 1998,21(1):50-55. (In Chinese)

Google Scholar

[9] Fan Yun Ge, Shi Zuo Qing, Shi Rong Fu. Ion Exchange and Adsorption,1998,14(1):31-35. (In Chinese)

Google Scholar

[10] Yu Shan Xin, Tang Chun Yan, Zhang Shang. Synthetic Chemistry ,1997,5(1):89-91. (In Chinese)

Google Scholar