Chemoselective reduction of pyrimidines. An access to enantiopure tetrahydropyrimidinones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. A New Chiral Auxiliary Derived from (2S)-Phenylglycinol: an Access to Enantiomerically Pure β-Amino Acids
2. Stereoselective α-Alkylation of New Chiral Auxiliaries: An Access to Enantiomerically Pure α- and α,β-Substituted β-Amino Acids
3. Enantioselective synthesis of α,β-substituted β-amino acids
4. An Efficient Synthesis of Pyrimidines from β-Amino Alcohols
5. An Efficient Synthesis of a New Series of Acyclonucleosides Starting from β-Amino Alcohols
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1. Chemoselective Reaction;Organic Stereochemistry;2015-06-26
2. Modified multicomponent Biginelli–Atwal reaction towards a straightforward construction of 5,6-dihydropyrimidin-4-ones;RSC Advances;2015
3. Synthesis and Bioactivity of Secondary Metabolites from Marine Sponges Containing Dibrominated Indolic Systems;Molecules;2012-05-21
4. ChemInform Abstract: Chemoselective Reduction of Pyrimidines. An Access to Enantiopure Tetrahydropyrimidinones.;ChemInform;2010-05-22
5. Total Synthesis and Antiproliferative Activity Screening of (±)-Aplicyanins A, B and E and Related Analogues;Journal of Medicinal Chemistry;2009-09-18
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