Bio‐inspired Domino oxa‐Michael/Diels–Alder/oxa‐Michael Dimerization of para ‐Quinols-Reference-Cited by-同舟云学术

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Bio‐inspired Domino oxa‐Michael/Diels–Alder/oxa‐Michael Dimerization of para ‐Quinols

Published:2018-04-25 Issue:21 Volume:57 Page:6198-6202
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Green Nicholas J.¹,Connolly Catherine A.¹,Rietdijk Koen P. W.¹,Nichol Gary S.¹,Duarte Fernanda¹^ORCID,Lawrence Andrew L.¹^ORCID

Affiliation:

1. EaStCHEM School of Chemistry University of Edinburgh Joseph Black Building David Brewster Road Edinburgh EH9 3FJ UK

Funder

Engineering and Physical Sciences Research Council

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201802125

Reference54 articles.

1.

2. Multi-Bond Forming Processes in Efficient Synthesis

3. Cyclohexadienone Ketals and Quinols: Four Building Blocks Potentially Useful for Enantioselective Synthesis

4. Select examples:

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3. Organocatalyzed Asymmetric Conjugate Addition of Alcohols to β‐Fluoroalkyl Vinylsulfones by Bifunctional Phosphonium Salt Catalyst;Chemistry – A European Journal;2024-06-18

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