Stereoselective Synthesis of Polysubstituted Tetrahydropyranones via Acid-Promoted Cyclization of β-Silyl-γ-ethylidene-γ-butyrolactones with Aldehydes and Ketones-Reference-Cited by-同舟云学术

Stereoselective Synthesis of Polysubstituted Tetrahydropyranones via Acid-Promoted Cyclization of β-Silyl-γ-ethylidene-γ-butyrolactones with Aldehydes and Ketones

Published:2021-08-13 Issue:17 Volume:86 Page:11884-11894
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ariyoshi Shoma¹,Sakaguchi Kazuhiko¹^ORCID,Nishimura Takahiro¹^ORCID

Affiliation:

1. Division of Molecular Materials Science, Graduate School of Science, Osaka City University, Sugimoto, Osaka 558-8585, Sumiyoshi, Japan

Funder

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01284

Reference32 articles.

1. Intramolecular Hetero-Michael Addition of β-Hydroxyenones for the Preparation of Highly Substituted Tetrahydropyranones

2. The oxa-Michael reaction: from recent developments to applications in natural product synthesis

3. A new strategy for the synthesis of substituted dihydropyrones and tetrahydropyrones via palladium-catalyzed coupling of thioesters

4. A short and flexible route to tetrahydropyran-4-ones via conjugated nitrile oxidescycloaddition and oxa-Michael cyclization: a concise diastereoselective total synthesis of (±)-diospongin A

5. Iron-Catalyzed Synthesis of C2 Aryl- and N-Heteroaryl-Substituted Tetrahydropyrans

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