Title of article
Synthetic studies on thiostrepton family of peptide antibiotics: synthesis of the dihydroquinoline portion of thiostrepton, the siomycins, and the thiopeptins
Author/Authors
Mori، نويسنده , , Tomonori and Satouchi، نويسنده , , Yukiko and Tohmiya، نويسنده , , Hiraku and Higashibayashi، نويسنده , , Shuhei and Hashimoto، نويسنده , , Kimiko and Nakata، نويسنده , , Masaya، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
6
From page
6417
To page
6422
Abstract
Synthesis of the dihydroquinoline portion of thiostrepton, the siomycins, and the thiopeptins, members of the thiostrepton family of peptide antibiotics, has been achieved featuring the one-pot olefination via the Matsumura–Boekelheide rearrangement “using trifluoromethanesulfonic anhydride and triethylamine” and the stereoselective addition reaction controlled by the stereocenter of the peri-position.
Keywords
Matsumura–Boekelheide rearrangement , stereoselective addition , Thiostrepton , Siomycins , dihydroquinoline
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1846642
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