Lewis acid mediated highly regioselective intramolecular cyclization for the synthesis of β-lapachone-Reference-Cited by-同舟云学术

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Lewis acid mediated highly regioselective intramolecular cyclization for the synthesis of β-lapachone

Published:2014-02 Issue:8 Volume:55 Page:1475-1478
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bian Jinlei,Deng Bang,Zhang Xiaojin,Hu Tianhan,Wang Nan,Wang Wei,Pei Haixiang,Xu Yu,Chu Hongxi,Li Xiang,Sun Haopeng,You Qidong

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Synthesis of quinoidal molecules: Strategies towards bioactive compounds with an emphasis on lapachones

2. Natural and synthetic quinones and their reduction by the quinone reductase enzyme NQO1: from synthetic organic chemistry to compounds with anticancer potential

3. Natural and Synthetic Naphthoquinones Active Against Trypanosoma Cruzi: An Initial Step Towards New Drugs for Chagas Disease

4. Synthesis and anti-inflammatory evaluations of β-lapachone derivatives

5. Antifungal activity of the naphthoquinone beta-lapachone against disseminated infection with Cryptococcus neoformans var. neoformans in dexamethasone-immunosuppressed Swiss mice

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1. Beta-lapachone: Natural occurrence, physicochemical properties, biological activities, toxicity and synthesis;Phytochemistry;2021-06

2. α‐ and β‐Lapachone Isomerization in Acidic Media: Insights from Experimental and Implicit/Explicit Solvation Approaches;ChemPlusChem;2018-12-13

3. Quinonoid compounds via reactions of lawsone and 2-aminonaphthoquinone with α-bromonitroalkenes and nitroallylic acetates: Structural diversity by C-ring modification and cytotoxic evaluation against cancer cells;European Journal of Medicinal Chemistry;2018-05

4. Addition Reactions: Polar Addition;Organic Reaction Mechanisms · 2014;2018-01-05

5. Construction of Cyclic Ether-Fused Tricyclic Naphthoquinone Derivatives by Intramolecular Cyclization Reaction;HETEROCYCLES;2018

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