Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5280458 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
The cyclic core portion containing the dehydropiperidine, dihydroquinoline, l-valine, and masked dehydroalanine (i.e., β-phenylselenoalanine) segments of the thiostrepton family of peptide antibiotics was synthesized via the consecutive coupling of these four segments followed by cyclization at the amide bond between the dehydropiperidine and masked dehydroalanine segments.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tomonori Mori, Hiraku Tohmiya, Yukiko Satouchi, Shuhei Higashibayashi, Kimiko Hashimoto, Masaya Nakata,