Organocatalyst-mediated asymmetric one-pot/two domino/three-component coupling reactions for the synthesis of <i>trans</i>-hydrindanes-Reference-Cited by-同舟云学术

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Organocatalyst-mediated asymmetric one-pot/two domino/three-component coupling reactions for the synthesis of trans-hydrindanes

Published:2024 Issue:15 Volume:15 Page:5627-5632
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Mori Naoki¹^ORCID,Tachibana Toshiki¹,Umekubo Nariyoshi¹^ORCID,Hayashi Yujiro¹^ORCID

Affiliation:

1. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan

Abstract

Highly substituted trans-hydrindanes were synthesized by the three-component coupling reactions of 1,3-diethyl 2-(2-oxopropylidene)propanedioate and two different α,β-unsaturated aldehydes catalyzed by diphenylprolinol silyl ether.

Funder

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC00193A

Reference50 articles.

1. Domino Reactions in Organic Synthesis

2. Domino Reactions , ed. L. F. Tietze , Wiley-VCH , Weinheim , 2014

3. Asymmetric Organocatalytic Michael/Michael/Henry Sequence to Construct Cyclohexanes with Six Vicinal Stereogenic Centers

4. Facile access to potent antiviral quinazoline heterocycles with fluorescence properties via merging metal-free domino reactions

5. Facile Access to Challenging ortho ‐Terphenyls via Merging Two Multi‐Step Domino Reactions in One‐Pot: A Joint Experimental/Theoretical Study

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