Features of oxa-bridge cleavage in hexahydro-3a,6-epoxyisoindol-1(4H)-ones: A concise method to access acetylisoindolones possessing anti-viral activity-Reference-Cited by-同舟云学术

Features of oxa-bridge cleavage in hexahydro-3a,6-epoxyisoindol-1(4H)-ones: A concise method to access acetylisoindolones possessing anti-viral activity

Published:2019-10 Issue:43 Volume:60 Page:151204
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Zaytsev Vladimir P.,Mertsalov Dmitriy F.,Chervyakova Lala V.,Krishna Gaddam,Zubkov Fedor I.,Dorovatovskii Pavel V.,Khrustalev Victor N.,Zarubaev Vladimir V.

Funder

Ministry of Education and Science of the Russian Federation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

1. Total Synthesis of (−)-Himalensine A

2. IMDAF Cascade Approach toward the Synthesis of the Alkaloid (±)-Minfiensine

3. Synthesis of Phenanthridine Derivatives Functionalized in the C-Ring by Means of IMDAF Reactions under Microwave or Conventional Heating Conditions

4. Intramolecular Diels–Alder Cycloaddition/Rearrangement Cascade of an Amidofuran Derivative for the Synthesis of (±)-Minfiensine

5. A Stereoselective and Atom-Efficient Approach to Multifunctionalized Five- and Six-Membered Rings via a Novel Michael-Initiated Intramolecular Diels−Alder Furan Reaction

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2. The short route to chalcogenurea-substituted 3a,6-epoxyisoindoles via an intramolecular Diels–Alder furan (IMDAF) reaction. Antibacterial and antifungal activity;New Journal of Chemistry;2024

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