An Efficient Synthesis of Enantiopure (R)-heteroarylpyrimidine Analogs
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-...
Main Authors: | Guo-Ming Zhao, Zhi-Bing Zheng, Dong-Mei Zhao, Xiao-Kui Wang, Guang-Qiang Xia, Xiu-Yan Yang, Song Li |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2013-09-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/18/9/11144 |
Similar Items
-
Enantiopure Cyclometalated Rh(III) and Ir(III) Complexes Displaying Rigid Configuration at Metal Center: Design, Structures, Chiroptical Properties and Role of the Iodide Ligand
by: Antoine Groué, et al.
Published: (2022-03-01) -
Synthesis and Insecticidal Evaluation of Chiral Neonicotinoids Analogs: The Laurel Wilt Case
by: Saúl A. Luna-Hernández, et al.
Published: (2021-07-01) -
Alcohol Dehydrogenases with anti‐Prelog Stereopreference in Synthesis of Enantiopure Alcohols
by: Prof. Dr. Musa M. Musa
Published: (2022-04-01) -
Chemo-Enzymatic Synthesis of Enantiopure β-Antagonist (<i>S</i>)-Betaxolol
by: Susanne Hansen Troøyen, et al.
Published: (2022-12-01) -
Chiral enantiopure bis(thio)ureas derived from TADDOL and their carboxylate complexation capacity
by: Gherase Dragos, et al.
Published: (2012-08-01)