Peptide Coupling Reactions with Phosphono-Phosphino Substituted γ-Thiapyrones -First Step to Unusual Peptides. -Chiral peptidosubstituted phosphono-phosphino γ-thiapyrones (III) are easily obtained by coupling of γ-thiapyrones (II) with protected amino acids (I) using perfluorophenyldiphenylphosphi
ChemInform Abstract: Synthesis and Chemical Reactions of New Phosphono-Phosphino Substituted γ-Thiapyrones.
✍ Scribed by R. NEIDLEIN; D. U. HAHN; W. KRAMER; C. KRIEGER
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Synthesis and Chemical Reactions of New Phosphono-Phosphino Substituted γ-Thiapyrones.
-The 1,3-dithietane-2,4-diylidenes (I) react with acylated acetonitriles to form γ-thiapyrones (III). Standard Boc-protection of (III) results in the reaction at the primary amino group and oxidative desulfurization leads to the γ-pyrones (VI). -(NEIDLEIN, R.;
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