The efficient preparation of α-substituted serine scaffolds as the chiral building blocks for the synthesis of SPT inhibitors
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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2. A stereoselective total synthesis of the HCl salts of mycestericins F, G and ent-F;Tetrahedron: Asymmetry;2013-02
3. A stereoselective synthesis of an α-substituted α-amino acid as a substructure for the construction of myriocin;Tetrahedron: Asymmetry;2012-04
4. Stereoselective synthesis of the polar part of mycestericins E and G;Chemical Papers;2011-01-01
5. A short stereoselective synthesis of the protected uracil 3′-epi-polyoxin C;Tetrahedron: Asymmetry;2011-01
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