Chemo-enzymatic synthesis of equisetin-Reference-Cited by-同舟云学术

Chemo-enzymatic synthesis of equisetin

Published:2017 Issue:34 Volume:53 Page:4695-4697
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Li Xiaojun¹²³⁴⁵,Zheng Qingfei⁶⁷⁸⁹⁵^ORCID,Yin Jun¹²³⁴⁵,Liu Wen⁶⁷⁸⁹⁵,Gao Shuanhu¹²³⁴⁵^ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes

2. School of Chemistry and Molecular Engineering

3. East China Normal University

4. Shanghai 200062

5. China

6. State Key Laboratory of Bioorganic and Natural Products Chemistry

7. Shanghai Institute of Organic Chemistry

8. Chinese Academy of Sciences

9. Shanghai 200032

Abstract

A chemo-enzymatic synthesis of equisetin was developed, in which the Diels–Alderase Fsa2 is used for catalyzing the key IMDA reaction stereoselectively.

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/2017/CC/C7CC01929G

Reference57 articles.

1. Naturally Occurring Tetramic Acids: Structure, Isolation, and Synthesis

2. Antibiotic Produced by Fusarium equiseti NRRL 5537

3. Characterization of the Fusarium toxin equisetin: the use of phenylboronates in structure assignment

4. Equisetin and a novel opposite stereochemical homolog phomasetin, two fungal metabolites as inhibitors of HIV-1 integrase

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