Synthesis of Cyclopentenones with C4-Quaternary Stereocenters via Stereospecific [3,3]-Sigmatropic Rearrangement and Applications in Total Synthesis of Sesquiterpenoids-Reference-Cited by-同舟云学术

Synthesis of Cyclopentenones with C4-Quaternary Stereocenters via Stereospecific [3,3]-Sigmatropic Rearrangement and Applications in Total Synthesis of Sesquiterpenoids

Published:2021-10-18 Issue:42 Volume:143 Page:17348-17353
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Zhou Weiping¹,Voituriez Arnaud¹^ORCID

Affiliation:

1. Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, 91198 Gif-sur-Yvette, France

Funder

China Scholarship Council

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.1c07966

Reference78 articles.

1. Metal-catalyzed asymmetric conjugate addition reaction: formation of quaternary stereocenters

2. Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis

3. Recent advances in palladium-catalysed asymmetric 1,4–additions of arylboronic acids to conjugated enones and chromones

4. All-carbon quaternary centers in natural products and medicinal chemistry: recent advances

5. Construction of all-carbon quaternary stereocenters by catalytic asymmetric conjugate addition to cyclic enones in natural product synthesis

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