Synthesis of Triarylpyridines in Thiopeptide Antibiotics by Using a C−H Arylation/Ring-Transformation Strategy-Reference-Cited by-同舟云学术

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Synthesis of Triarylpyridines in Thiopeptide Antibiotics by Using a C−H Arylation/Ring-Transformation Strategy

Published:2016-02-18 Issue:13 Volume:22 Page:4384-4388
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Amaike Kazuma¹²,Itami Kenichiro¹²³,Yamaguchi Junichiro¹²^ORCID

Affiliation:

1. Institute of Transformative Bio-Molecules (WPI-ITbM); Nagoya University; Chikusa Nagoya 464-8601 Japan

2. Department of Chemistry; Graduate School of Science; Nagoya University; Chikusa Nagoya 464-8602 Japan

3. JST, ERATO; Itami Molecular Nanocarbon Project; Chikusa Nagoya 464-8602 Japan

Funder

Grant-in-Aid for Scientific Research on Innovative Areas

MEXT

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201600351/fullpdf

Reference76 articles.

1. From Peptide Precursors to Oxazole and Thiazole-Containing Peptide Antibiotics: Microcin B17 Synthase

2. Thiopeptide Antibiotics

3. From Amino Acids to Heteroaromatics—Thiopeptide Antibiotics, Nature's Heterocyclic Peptides

4. Von Aminosäuren zu Heteroarenen – Thiopeptid-Antibiotika als heterocyclische Peptide aus der Natur

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