Rearrangement of azidoquinones IV. Ring expansion of 4-azido-1, 2-naphthoquinone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Rearrangements of azidoquinones II. Stereoselective acid-catalyzed rearrangement of azidoquinones to γ-alkylidene (arylidene) -Δga,gb-butenolides
2. C, H-Analysis for all new compounds are consistent with their proposed formulations.
3. Synthesis of 2,5-H-2,5-azepindiones from quinones and hydrazoic acid
4. Synthesis of 2,5-2,5-azepindiones by the reaction of quinones with hydrazoic acid
5. Schmidt reaction of hydroxyquinones
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1. Tandem Denitrogenation Oxidative Coupling Reaction of Phenyl Vinyl Azides and Cyclic Ethers Under Metal‐Free Conditions;ChemistrySelect;2023-01-02
2. 1,2-Naphthoquinone-4-sulfonic acid salts in organic synthesis;Beilstein Journal of Organic Chemistry;2022-01-05
3. S-triggered Schmidt-type rearrangement of vinyl azides to access N-aryl-(trifluoromethylsulfinyl)acetamides;Organic Chemistry Frontiers;2022
4. One‐Pot Synthesis of Enantioenriched β‐Amino Secondary Amides via an Enantioselective [4+2] Cycloaddition Reaction of Vinyl Azides with N ‐Acyl Imines Catalyzed by a Chiral Brønsted Acid;Chemistry – A European Journal;2020-06-17
5. A bench-stable low-molecular-weight vinyl azide surrogate for a cascade reaction: facile access to novel N-vinyl-1,2,3-triazoles;Organic Chemistry Frontiers;2020
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