Literature DB >> 14714759

Studies towards the large scale chemical synthesis of the precursors of ribonucleosides-3',4',5',5''-2H4 and -2',3',4',5',5''-2H5.

András Földesi1, Jyoti Chattopadhyaya.   

Abstract

A summary delineating the large scale synthetic studies to prepare labeled precursors of ribonucleosides-3',4',5',5''-2H4 and -2',3',4',5',5''-2H5 from D-glucose is presented. The recycling of deuterium-labeled by-products has been devised to give a high overall yield of the intermediates and an expedient protocol has been elaborated for the conversion of 3-O-benzyl-alpha,beta-D-allofuranose-3,4-d2 6 to 1-O-methyl-3-O-benzyl-2-O-t-butyldimethylsilyl-alpha,beta-D-ribofuranose-3,4,5,5'-d4 16 (precursor of ribonucleosides-3',4',5',5''-2H4) or to 1-O-methyl-3,5-di-O-benzyl-alpha,beta-D-ribofuranose-3,4,5,5'-d4 18 (precursor of ribonucleosides-3',4',5',5''-2H4).

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Year:  2003        PMID: 14714759     DOI: 10.1081/ncn-120026632

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  1 in total

1.  Synthesis and anti-SARS-CoV-2 activity of deuterated GS-441524 analogs.

Authors:  Wei Zheng; Tianwen Hu; Yumin Zhang; Daibao Wei; Yuanchao Xie; Jingshan Shen
Journal:  Tetrahedron Lett       Date:  2022-07-09       Impact factor: 2.032

  1 in total

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