Unusual Acetylation-Elimination in the Formation of Tetronate Antibiotics-Reference-Cited by-同舟云学术

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Unusual Acetylation-Elimination in the Formation of Tetronate Antibiotics

Published:2013-04-18 Issue:22 Volume:52 Page:5785-5788
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Kanchanabanca Chompoonik,Tao Weixin,Hong Hui,Liu Yajing,Hahn Frank,Samborskyy Markiyan,Deng Zixin,Sun Yuhui,Leadlay Peter F.

Funder

BBSRC

Ministry of Science and Technology

National Natural Science Foundation of China

Ministry of Education

China Postdoctoral Science Foundation

EU

Deutsche Forschungsgemeinschaft

Alexander von Humboldt Foundation

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/anie.201301680/fullpdf

Reference20 articles.

1. Domino syntheses of bioactive tetronic and tetramic acids

2. Analysis of the Tetronomycin Gene Cluster: Insights into the Biosynthesis of a Polyether Tetronate Antibiotic

3. Structure of antibiotic M139603; X-ray crystal structure of the 4-bromo-3,5-dinitrobenzoyl derivative

4. Structures of agglomerins.

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1. Antibiotic origami: selective formation of spirotetronates in abyssomicin biosynthesis;Chemical Science;2024

2. Discovery of Tetronate-Containing Kongjuemycins from a Coral-Associated Actinomycete and Elucidation of Their Biosynthetic Origin;Organic Letters;2023-08-22

3. A Widespread Glycosidase Confers Lobophorin Resistance and Host‐Dependent Structural Diversity;Angewandte Chemie;2023-05-09

4. A Widespread Glycosidase Confers Lobophorin Resistance and Host‐Dependent Structural Diversity;Angewandte Chemie International Edition;2023-05-09

5. Characterization of the P450 Monooxygenase LobP1 as C‐32 Hydroxylase in Lobophorin Biosynthesis;Chinese Journal of Chemistry;2023-03-30

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