Asymmetric Total Synthesis of Fusarentin 6-Methyl Ether and Its Biomimetic Transformation into Fusarentin 6,7-Dimethyl Ether, 7-O-Demethylmonocerin, and (+)-Monocerin-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of Fusarentin 6-Methyl Ether and Its Biomimetic Transformation into Fusarentin 6,7-Dimethyl Ether, 7-O-Demethylmonocerin, and (+)-Monocerin

Published:2013-06-07 Issue:12 Volume:78 Page:6338-6343
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Fang Bowen¹,Xie Xingang¹,Zhao Changgui¹,Jing Peng¹,Li Huilin¹,Wang Zhengshen¹,Gu Jixiang¹,She Xuegong¹²

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou, Gansu 730000, People’s Republic of China

2. State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, Gansu 730000, People’s Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo400760q

Reference24 articles.

1. Metabolic products of Fusarium larvarum fuckel. The fusarentins and the absolute configuration of monocerin

2. Metabolites of Helminthosporium monoceras: structures of monocerin and related benzopyrans

3. Biosynthesis of monocerin. Incorporation of 2H-, 13C-, and 18O-labelled acetates by Drechslera ravenelii

4. Monocerin in Exserohilum turcicum isolates from maize and a study of its phytotoxicity

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