Computational Investigation of the Mechanism of Diels–Alderase PyrI4-Reference-Cited by-同舟云学术

Computational Investigation of the Mechanism of Diels–Alderase PyrI4

Published:2020-11-14 Issue:47 Volume:142 Page:20232-20239
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zou Yike¹^ORCID,Yang Song¹,Sanders Jacob N.¹^ORCID,Li Wei¹,Yu Peiyuan¹,Wang Hongbo²,Tang Zhijun²,Liu Wen²^ORCID,Houk K. N.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, United States

2. State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

Funder

Division of Chemistry

National Institute of General Medical Sciences

Chinese Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.0c10813

Reference39 articles.

1. The Diels-Alder Reaction in Total Synthesis

2. Enzymatic activity catalysing exo-selective Diels–Alder reaction in solanapyrone biosynthesis

3. A novel bicyclo(2.2.2)octane skeleton diterpene, obtunone, from the heartwood of Chamaecyparis obtusa var. formosana.

4. Sequential Diels–Alder Reaction/Rearrangement Sequence: Synthesis of Functionalized Bicyclo[2.2.1]heptane Derivatives and Revision of Their Relative Configuration

5. Biosynthesis of the Tetramic Acids Sch210971 and Sch210972

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