Intramolecular 1,5-cyclization of ylides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. 1.5‐Dipolare Cyclisierungen, I. Begriffsbestimmung und Beiträge zur Imidazid/Tetrazol‐Tautomerie
2. Thermische Stabilität und aromatischer Charakter: Ringöffnungen der Azole
3. 1.5‐Dipolare Cyclisierungen, III. Kondensierte Triazole aus konjugierten Nitriliminen. Struktur und Stabilität der Produkte aus N ‐acylierten cyclischen Amidrazonen und Thionylchlorid
4. Hydrazones—IV
5. Synthesis of 2,5-disubstituted thiophenes
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1. The Baylis–Hillman reaction: a new continent in organic chemistry – our philosophy, vision and over three decades of research;New Journal of Chemistry;2018
2. Synthesis of Functionalized Pyrazolo[1,5-a]pyridines: [3+2] Cycloaddition of N-Aminopyridines and α,β-Unsaturated Carbonyl Compounds/Alkenes at Room Temperature;Synthesis;2017-03-14
3. A Modular Synthesis of Polysubstituted Indolizines;European Journal of Organic Chemistry;2012-07-04
4. Features of reactions of quaternary salts derived from (4Z)-5-(bromomethyl)-2,2,6,6-tetra-methylhept-4-en-3-one. Synthesis of azolo[a]azepine and indolizine derivatives;Chemistry of Heterocyclic Compounds;2012-05
5. Reactions of Pyridinium N-Ylides and Their Related Pyridinium Salts;HETEROCYCLES;2012
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