A concise total synthesis of (−)-indolactam V-Reference-Cited by-同舟云学术

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A concise total synthesis of (−)-indolactam V

Published:2015-06 Issue:23 Volume:71 Page:3833-3837
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Noji Toshiharu,Okano Kentaro,Tokuyama Hidetoshi

Funder

Funding Program for Next Generation World-Leading Researchers

JSPS KAKENHI

Platform for Drug Discovery, Informatics, and Structural Life Science

Scientific Research on Innovative Areas

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference67 articles.

1. Indole alkaloids: dihydroteleocidin B, teleocidin, and lyngbyatoxin A as members of a new class of tumor promoters.

2. Pendolmycin, a New Tumor Promoter of the Teleocidin A Class on Skin of CD-1 Mice

3. GCN2 Kinase in T Cells Mediates Proliferative Arrest and Anergy Induction in Response to Indoleamine 2,3-Dioxygenase

4. A New Toxic Substance, Teleocidin, Produced by Streptonayces

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1. Structure, biosynthesis and activity of indolactam alkaloids;The Alkaloids: Chemistry and Biology;2024

2. Functions, Structures, and Engineering of the Teleocidin Biosynthetic Enzymes;Chemical and Pharmaceutical Bulletin;2023-03-01

3. Indolactam Dipeptides as Nanomolar Gli Inhibitors;ACS Medicinal Chemistry Letters;2022-06-03

4. Use of Non‐Aromatic Hydrophobic α‐Amino Acids (α‐AA) and Non‐Amino Acid Derived Synthons: Comparative Studies Towards Total Syntheses of Selected Bioactive Natural Alkaloids;ChemistrySelect;2022-03-08

5. Recent developments in the utility of saturated azaheterocycles in peptidomimetics;Organic & Biomolecular Chemistry;2022

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