Diastereoselective synthesis of tetrahydropyranes <i>via</i> Ag(<scp>i</scp>)-initiated dimerization of cinnamyl ethers-Reference-Cited by-同舟云学术

Diastereoselective synthesis of tetrahydropyranes via Ag(i)-initiated dimerization of cinnamyl ethers

Published:2022 Issue:47 Volume:20 Page:9287-9291
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Ruggeri Davide¹^ORCID,Motti Elena¹²^ORCID,Della Ca’ Nicola¹²^ORCID,Maestri Giovanni¹²^ORCID

Affiliation:

1. Università di Parma, Dipartimento di Scienze Chimiche, della Vita e della Sostenibilità Ambientale, Parco Area delle Scienze 17/A, 43124 Parma, Italy

2. CIRCC (Interuniversity Consortium on Chemical Reactivity and Catalysis), via Celso Ulpiani 27, 70126 Bari, Italy

Abstract

From simple linear cinnamyl ethers to complex tetrahydropyranes with high diastereocontrol via Ag(i) initiation of a cationic chain.

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Università degli Studi di Parma

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01876D

Reference30 articles.

1. Pharmacological use of a novel scaffold, anomeric N,N-diarylamino tetrahydropyran: molecular similarity search, chemocentric target profiling, and experimental evidence

2. New direct inhibitors of InhA with antimycobacterial activity based on a tetrahydropyran scaffold

3. First Enantioselective Total Synthesis of (−)-Centrolobine

4. Total Syntheses of Centrolobines: A Two‐Decade Journey

5. Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product

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