Total synthesis of streptovertidione and bioinspired transformation to streptovertidine A and formicapyridine A-Reference-Cited by-同舟云学术

Total synthesis of streptovertidione and bioinspired transformation to streptovertidine A and formicapyridine A

Published:2022 Issue:26 Volume:58 Page:4239-4242
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Quan¹,He Haibing²,Gao Shuanhu¹²^ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 3663N Zhongshan Road, Shanghai 200062, China

2. Shanghai Frontiers Science Center of Molecule Intelligent Syntheses, School of Chemistry and Molecular Engineering, East China Normal University, 3663N Zhongshan Road, Shanghai 200062, China

Abstract

We report herein a concise total synthesis of streptovertidione, and its transformation to streptovertidine A and formicapyridine A through a bioinspired pyridination.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Shanghai Educational Development Foundation

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CC/D2CC00947A

Reference34 articles.

1. Functional analysis of environmental DNA-derived type II polyketide synthases reveals structurally diverse secondary metabolites

2. Environmental DNA-Encoded Antibiotics Fasamycins A and B Inhibit FabF in Type II Fatty Acid Biosynthesis

3. Discovery of New Antibacterial Accramycins from a Genetic Variant of the Soil Bacterium, Streptomyces sp. MA37

4. Formicamycins, antibacterial polyketides produced by Streptomyces formicae isolated from African Tetraponera plant-ants

5. Re-wiring the regulation of the formicamycin biosynthetic gene cluster to enable the development of promising antibacterial compounds

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Total Synthesis of the Phenylnaphthacenoid Type II Polyketide Antibiotic Formicamycin H via Regioselective Ruthenium-Catalyzed Hydrogen Auto-Transfer [4 + 2] Cycloaddition;Journal of the American Chemical Society;2024-09-12

2. Synthesis of 2,5‐Disubstituted Pyridines using the Gold(I)‐Catalyzed Cycloisomerization of 1‐Bromoalkynes as Key Step;European Journal of Organic Chemistry;2024-01-10

3. Asymmetric Total Synthesis of Hasubanan Alkaloids: Periglaucines A–C, N,O ‐Dimethyloxostephine and Oxostephabenine;Angewandte Chemie International Edition;2022-12-02

4. Asymmetric Total Synthesis of Hasubanan Alkaloids: Periglaucines A–C, N,O ‐Dimethyloxostephine and Oxostephabenine;Angewandte Chemie;2022-12-02

5. Nickel^II-catalyzed asymmetric photoenolization/Mannich reaction of (2-alkylphenyl) ketones;Chemical Science;2022