Metal-free synthesis of dihydrofuran derivatives as anti-vicinal amino alcohol isosteres-Reference-Cited by-同舟云学术

Metal-free synthesis of dihydrofuran derivatives as anti-vicinal amino alcohol isosteres

Published:2023 Issue:5 Volume:21 Page:960-965
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Nangunuri Bhargav Gupta¹,Shirke Rajendra P.¹,Kim Mi-hyun¹^ORCID

Affiliation:

1. Gachon Institute of Pharmaceutical Science & Department of Pharmacy, College of Pharmacy, Gachon University, 191 Hambakmoeiro, Yeonsu-gu, Incheon, Republic of Korea

Abstract

Dihydrofuran cores are commonly incorporated into synthetically and pharmacologically significant scaffolds in natural product and drug discovery chemistry.

Funder

National Research Foundation of Korea

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D2OB02077G

Reference58 articles.

1. Stereoselective Ring Expansion of Vinyl Oxiranes: Mechanistic Insights and Natural Product Total Synthesis

2. Recent applications in natural product synthesis of dihydrofuran and -pyran formation by ring-closing alkene metathesis

3. Rh-Catalyzed oxidative homo-coupling cyclization of 2,3-allenols to conjugated furylenones

4. One-pot catalytic selective synthesis of 1,4-butanediol from 1,4-anhydroerythritol and hydrogen

5. Recent reports on the synthesis of γ-butenolide, γ-alkylidenebutenolide frameworks, and related natural products

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