A convenient synthesis of -(5′-deoxy-5′-adenosyl)- (±) -2-methylhomocysteine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Synthesis of potential inhibitors of transmethylases
2. Analogs of S-adenosylhomocysteine as potential inhibitors of biological transmethylation. Inhibition of several methylases by S-tubercidinylhomocysteine
3. S-Adenosyl-L-methionine-dependent macromolecule methyltransferases: potential targets for the design of chemotherapeutic agents
4. Studies on the Chemical Synthesis of Potential Antimetabolites. 31.1A Novel Synthesis of 1-Deazaadenosine and Its Conversion to 5′-Deoxy-5′-Isobutylthio-1-Deazaadenosine (1-Deaza-Siba) and S-(1-Deazaadenosyl)-Homocysteine (1-DEAZA-SAH)
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1. Umpolung Reaction of Imine Analogues and Their Development into Biologically Active Compounds;Journal of Synthetic Organic Chemistry, Japan;2024-07-01
2. S-Adenosylhomocysteine Analogue of a Fairy Chemical, Imidazole-4-carboxamide, as its Metabolite in Rice and Yeast and Synthetic Investigations of Related Compounds;Journal of Natural Products;2021-01-22
3. Dissociation of [b5]+ ions containing an α-methyltryptophan and four alanine residues; losses of CO2 and the oxazolone ring;International Journal of Mass Spectrometry;2018-06
4. Synthesis and characterization ofSe-adenosyl-L-selenohomocysteine selenoxide;Journal of Sulfur Chemistry;2014-11-24
5. Synthesis of γ,δ-unsaturated quaternary α-alkylamino acids using umpolung reaction and Claisen rearrangement;Tetrahedron Letters;2012-04
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