Stereocontrolled and time-honored access to piperidine- and pyrrolidine-fused 3-methylenetetrahydropyrans using lactam-tethered alkenols-Reference-Cited by-同舟云学术

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Stereocontrolled and time-honored access to piperidine- and pyrrolidine-fused 3-methylenetetrahydropyrans using lactam-tethered alkenols

Published:2024 Issue:37 Volume:14 Page:26913-26919
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Beng Timothy K.¹^ORCID,Anosike Ifeyinwa S.¹,Kaur Jasleen¹

Affiliation:

1. Department of Chemistry, Central Washington University, Ellensburg, WA 98926, USA

Abstract

Two cascade approaches featuring bromocycloetherification-elimination or dehydrogenative cycloetherification-isomerization of lactam-tethered alkenols have facilitated the stereocontrolled synthesis of lactam-fused 3-methylenetetrahydropyrans.

Funder

Central Washington University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/RA/D4RA04916K

Reference73 articles.

1. Hodgsonox, a New Class of Sesquiterpene from the Liverwort Lepidolaena hodgsoniae. Isolation Directed by Insecticidal Activity

2. SN/SN‘ Competition: Selective Access to New 10-Fluoro Artemisinins

3. Deoxyartemisinin Derivatives from Photooxygenation of Anhydrodeoxydihydroartemisinin and Their Cytotoxic Evaluation

4. Iridoids and sesquiterpenoids of Valeriana stenoptera and their effects on NGF-induced neurite outgrowth in PC12 cells

5. Rhopaloic acid A: A novel norsesterterpene from a marine sponge, Rhopaloeides sp., which inhibits gastrulation of starfish embryos

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