Molecules 2013, 18(9), 11144-11152; doi:10.3390/molecules180911144

An Efficient Synthesis of Enantiopure (R)-heteroarylpyrimidine Analogs

1,2,†, 2,†, 2, 2, 2, 2,* email and 1,2,* email
Received: 23 August 2013; in revised form: 3 September 2013 / Accepted: 4 September 2013 / Published: 11 September 2013
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: An efficient synthesis of enantiopure (R)-heteroarylpyrimidine analogs is described here, which involves introduction of a chiral group, formation and separation of diasteroisomers and final transformation of an amide to an ester. The absolute configuration of the enantiopure HAPs is confirmed by X-ray analysis of their intermediates.
Keywords: anti-HBV; enantiopure; (R)-heteroarylpyrimidines; chiral separation; diastereomer
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MDPI and ACS Style

Yang, X.-Y.; Xia, G.-Q.; Wang, X.-K.; Zheng, Z.-B.; Zhao, D.-M.; Zhao, G.-M.; Li, S. An Efficient Synthesis of Enantiopure (R)-heteroarylpyrimidine Analogs. Molecules 2013, 18, 11144-11152.

AMA Style

Yang X-Y, Xia G-Q, Wang X-K, Zheng Z-B, Zhao D-M, Zhao G-M, Li S. An Efficient Synthesis of Enantiopure (R)-heteroarylpyrimidine Analogs. Molecules. 2013; 18(9):11144-11152.

Chicago/Turabian Style

Yang, Xiu-Yan; Xia, Guang-Qiang; Wang, Xiao-Kui; Zheng, Zhi-Bing; Zhao, Dong-Mei; Zhao, Guo-Ming; Li, Song. 2013. "An Efficient Synthesis of Enantiopure (R)-heteroarylpyrimidine Analogs." Molecules 18, no. 9: 11144-11152.

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