Ring-opening reactions of benzotriazoles with Wittig reagents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. The reaction of benzylidenetriphenylphosphoranes with benzenediazonium-2-carboxylate
2. Synthesis of 3,4,6-trisubstituted cinnolines by intramolecular wittig reaction ofortho-carbonyl substituted arylazomethylenetriphenylphosphoranes
3. Stereochemical aspects of base-promoted reactions of o-alkenyl substituted arylhydrazonoyl chlorides with triphenylphosphine
4. A novel synthesis of 5-chloro-3-methoxycarbonyl-1-arylpyrazoles from arylazomethylenetriphenylphosphoranes
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1. Benzotriazole ring cleavage methodology under free radical condition: an ample opportunity in organic synthesis;Organic Radicals;2024
2. Selective N–N or N–S bond cleavage of 1-trifluoromethyl benzotriazoles enables divergent synthesis of 1,2,4-benzotriazines and benzotriazoles;Organic Chemistry Frontiers;2023
3. Metal-Free [5 + 1] Cycloaddition–Aromatization of Benzotriazoles and Sulfur Ylides to Construct 1,2,4-Benzotriazines;Organic Letters;2022-08-05
4. Renaissance of Ring‐Opening Chemistry of Benzotriazoles: New Wine in an Old Bottle;The Chemical Record;2020-01-09
5. Construction of 3-aryl-1,2,4-benzotriazines via unprecedented rearrangement of bis(benzotriazol-1-yl)methylarenes;Tetrahedron Letters;2010-12
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