A radical S-adenosyl-L-methionine enzyme and a methyltransferase catalyze cyclopropane formation in natural product biosynthesis-Reference-Cited by-同舟云学术

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A radical S-adenosyl-L-methionine enzyme and a methyltransferase catalyze cyclopropane formation in natural product biosynthesis

Published:2018-07-17 Issue:1 Volume:9 Page:
ISSN:2041-1723
Container-title:Nature Communications
language:en
Short-container-title:Nat Commun

Author:

Jin Wen-Bing^ORCID,Wu Sheng,Jian Xiao-Hong,Yuan Hua^ORCID,Tang Gong-Li^ORCID

Funder

National Natural Science Foundation of China (National Science Foundation of China)

Chinese Academy of Sciences (CAS)

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

Link

http://www.nature.com/articles/s41467-018-05217-1.pdf

Reference50 articles.

1. Chen, D. Y., Pouwer, R. H. & Richard, J. A. Recent advances in the total synthesis of cyclopropane-containing natural products. Chem. Soc. Rev. 41, 4631–4642 (2012).

2. Ebner, C. & Carreira, E. M. Cyclopropanation strategies in recent total syntheses. Chem. Rev. 117, 11651–11679 (2017).

3. Talele, T. T. The “cyclopropyl fragment” is a versatile player that frequently appears in preclinical/clinical drug molecules. J. Med. Chem. 59, 8712–8756 (2016).

4. Thibodeaux, C. J., Chang, W. C. & Liu, H. W. Enzymatic chemistry of cyclopropane, epoxide, and aziridine biosynthesis. Chem. Rev. 112, 1681–1709 (2012).

5. Jakubczyk, D. et al. Discovery and reconstitution of the cycloclavine biosynthetic pathway–enzymatic formation of a cyclopropyl group. Angew. Chem. Int. Ed. Engl. 54, 5117–5121 (2015).

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