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

Heterocycles ◽  
2002 ◽  
Vol 57 (1) ◽  
pp. 111 ◽  
Author(s):  
Kimiko Hashimoto ◽  
Syuhei Higashibayashi ◽  
Tomonori Mori ◽  
Kazuyuki Shinko ◽  
Masaya Nakata
Keyword(s):  
Peptide Antibiotics ◽  
Synthetic Studies

Synthetic studies on thiostrepton family of peptide antibiotics: synthesis of the dihydroquinoline portion of thiostrepton, the siomycins, and the thiopeptins

2005 ◽  
Vol 46 (38) ◽  
pp. 6417-6422 ◽  
Author(s):  
Tomonori Mori ◽  
Yukiko Satouchi ◽  
Hiraku Tohmiya ◽  
Shuhei Higashibayashi ◽  
Kimiko Hashimoto ◽  
...  
Keyword(s):  
Peptide Antibiotics ◽  
Synthetic Studies

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

2005 ◽  
Vol 46 (38) ◽  
pp. 6423-6427 ◽  
Author(s):  
Tomonori Mori ◽  
Hiraku Tohmiya ◽  
Yukiko Satouchi ◽  
Shuhei Higashibayashi ◽  
Kimiko Hashimoto ◽  
...  
Keyword(s):  
Peptide Antibiotics ◽  
Synthetic Studies

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

2004 ◽  
Vol 45 (19) ◽  
pp. 3707-3712 ◽  
Author(s):  
Shuhei Higashibayashi ◽  
Mitsunori Kohno ◽  
Taiji Goto ◽  
Kengo Suzuki ◽  
Tomonori Mori ◽  
...  
Keyword(s):  
Peptide Antibiotics ◽  
Synthetic Studies ◽  
Dehydroamino Acid

Synthetic Studies on Thiostrepton Family of Peptide Antibiotics: Synthesis of the Pentapeptide Segment Containing Dihydroxyisoleucine, Thiazoline and Dehydroamino Acid.

ChemInform ◽  
2004 ◽  
Vol 35 (33) ◽  
Author(s):  
Shuhei Higashibayashi ◽  
Mitsunori Kohno ◽  
Taiji Goto ◽  
Kengo Suzuki ◽  
Tomonori Mori ◽  
...  
Keyword(s):  
Peptide Antibiotics ◽  
Synthetic Studies ◽  
Dehydroamino Acid

Synthetic studies toward inducamide C

2021 ◽  
Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry
Keyword(s):  
Natural Product ◽  
Structural Revision ◽  
Synthetic Studies

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.

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