One-Pot Stereoselective Synthesis of Furantetrahydroquinoline Derivatives Using <scp>d</scp>/<scp>l</scp>-Ribose with a 2,3-<i>O</i>-Isopropylidene Group-Reference-Cited by-同舟云学术

One-Pot Stereoselective Synthesis of Furantetrahydroquinoline Derivatives Using d/l-Ribose with a 2,3-O-Isopropylidene Group

Published:2023-08-18 Issue:17 Volume:88 Page:12445-12450
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wu Jilai¹^ORCID,Xie Song¹,Zhou Likai¹²,Liu Yixuan¹,Cui Yaxin¹,Huang Xiaoyan¹,Wei Chao¹,Li Xiaoliu¹,Zhang Chunfang¹^ORCID,Chen Hua¹

Affiliation:

1. Key Laboratory of Chemical Biology of Hebei Province, College of Chemistry and Material Science, Hebei University, Baoding, Hebei 071002, P. R. China

2. College of Chemistry and Chemical Engineering, Xingtai University, Xingtai, Hebei 054001, China

Funder

Natural Science Foundation of Hebei Province

Hebei University

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c01187

Reference27 articles.

1. Structure and Total Synthesis of Aspernigerin: A Novel Cytotoxic Endophyte Metabolite

2. Two novel benzastatin derivatives, JBIR-67 and JBIR-73, isolated from Streptomyces sp. RI18

3. Helquinoline, a New Tetrahydroquinoline Antibiotic from Janibacter limosus Hel 1.

4. Synthesis, absolute configuration and intermediates of 9-fluoro-6,7-dihydro-5-methyl-1-oxo-1H,5H-benzo[i,j]quinolizine-2-carboxylic acid (flumequine)

5. Protein Farnesyltransferase Inhibitors Exhibit Potent Antimalarial Activity

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