Synthetic studies on thiostrepton family of peptide antibiotics: synthesis of the cyclic core portion containing the dehydropiperidine, dihydroquinoline, l-valine, and masked dehydroalanine segments-Reference-Cited by-同舟云学术

Synthetic studies on thiostrepton family of peptide antibiotics: synthesis of the cyclic core portion containing the dehydropiperidine, dihydroquinoline, l-valine, and masked dehydroalanine segments

Published:2005-09 Issue:38 Volume:46 Page:6423-6427
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Mori Tomonori,Tohmiya Hiraku,Satouchi Yukiko,Higashibayashi Shuhei,Hashimoto Kimiko,Nakata Masaya

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference42 articles.

1. Mori, T.; Satouchi, Y.; Tohmiya, H.; Higashibayashi, S.; Hashimoto, K.; Nakata, M, preceding paper, Tetrahedron Lett. 2005, 46, doi:10.1016/j.tetlet.2005.07.121.

2. Synthetic studies on the thiostrepton family of peptide antibiotics: synthesis of the tetrasubstituted dehydropiperidine and piperidine cores

3. Synthetic Studies on Thiostrepton Family of Peptide Antibiotics: Synthesis of the Tetrasubstituted Dihydroquinoline Portion of Siomycin D1

4. Synthetic studies on thiostrepton family of peptide antibiotics: synthesis of the pentapeptide segment containing dihydroxyisoleucine, thiazoline and dehydroamino acid

5. A Convenient Synthesis of Methyl 2-[2-(1-Amino)ethenyl-bithiazolyl] thiazoline-4-carboxylate, an Important Skeleton of Cyclothiazomycin

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