Molecular and Computational Bases for Spirofuranone Formation in Setosusin Biosynthesis-Reference-Cited by-同舟云学术

Molecular and Computational Bases for Spirofuranone Formation in Setosusin Biosynthesis

Published:2021-10-13 Issue:42 Volume:143 Page:17708-17715
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wei Xingxing¹^ORCID,Matsuyama Taro²,Sato Hajime²³^ORCID,Yan Dexiu¹,Chan Pui Man¹,Miyamoto Kazunori²^ORCID,Uchiyama Masanobu²⁴^ORCID,Matsuda Yudai¹^ORCID

Affiliation:

1. Department of Chemistry, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong SAR, China

2. Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan

3. Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, 4-4-37 Takeda, Kofu, Yamanashi 400-8510, Japan

4. Research Initiative for Supra-Materials (RISM), Shinshu University, 3-15-1 Tokida, Ueda, Nagano 386-8567, Japan

Funder

Research Grants Council, University Grants Committee

Ministry of Education, Culture, Sports, Science and Technology

Japan Society for the Promotion of Science

Japan Science and Technology Agency

City University of Hong Kong

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.1c08336

Reference39 articles.

1. Oxidative rearrangements during fungal biosynthesis

2. Oxidative Cyclization in Natural Product Biosynthesis

3. Formation and Cleavage of C–C Bonds by Enzymatic Oxidation–Reduction Reactions

4. Expansion of chemical space for natural products by uncommon P450 reactions

5. Recent examples of α-ketoglutarate-dependent mononuclear non-haem iron enzymes in natural product biosyntheses

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