Reductive coupling of (azulen-1-yl)carbonyl compounds by low-valent titanium; pinacol/pinacolone rearrangement versus pinacol and alkene generation
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Evolution of the stereoselective pinacol coupling reaction
2. Low-Valent Titanium-Mediated Reductive Coupling of Carbonyl Compounds
3. Magnesium- and titanium-induced reductive coupling of carbonyl compounds: efficient syntheses of pinacols and alkenes
4. A comparative study of the McMurry reaction utilizing [HTiCl(THF) –0.5]x, TiCl3(DME)1.5Zn(Cu) and TiCl2 · LiCl as coupling reagents
5. New Developments in the Chemistry of Low-Valent Titanium
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1. Cation Bridge Mediating Homo- and Cross-Coupling in Copper-Catalyzed Reductive Coupling of Benzaldehyde and Benzophenone;Inorganic Chemistry;2022-10-31
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3. RING SIZE EFFECT IN McMURRY CYCLIZATION OF 1,ω-DI((AZULEN-1-YL)-CARBONYL)ALKANES;REV ROUM CHIM;2020
4. Tuning the Selectivity: Study of Solvent-Free Acid-Mediated Pinacolic-Pinacolone Rearrangement under Microwave Irradiation;ChemistrySelect;2018-09-27
5. Synthesis of azulenic compounds with a homo- or hetero-atomic double bond at position 1;Arkivoc;2018-06-09
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