Synthesis and alkali metal reduction of 1,1-diarylspiro[2.4]hepta-4,6-dienes. Generation of homopentafulvene dianions
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Vielelektronenliganden, XV. Über die Reaktivität von Spiro[2.4]hepta‐4,6‐dien gegen Organolithium‐ und Organoelementlithium‐Verbindungen
2. Metallinduzierte CC‐Einfachbindungsspaltung 5,5‐dialkylsubstituierter Cyclopentadiene durch Metallcarbonylkomplexe der 6. Nebengruppe
3. Metallalkyle durch nucleophile Cyclopropan‐Ringöffnung am Spiro[2.4]hepta‐4,6‐dien‐System mit Natrium‐[dicarbonyl‐(η 5 ‐cyclopentadienyl)ferrat]
4. Synthesis and crystal structure of [Ru(η5-C5H4CH4CH2PPh2)(PPh3)Cl], a compound having a cyclopentadienyl proton with a chemical shift of δ 1.91 p.p.m.
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spiro[2.4]hepta-4,6-dienes: synthesis and application in organic synthesis;Russian Chemical Reviews;2016-03-31
2. ChemInform Abstract: Synthesis and Alkali Metal Reduction of 1,1-Diarylspiro(2.4)hepta-4,6- dienes. Generation of Homopentafulvene Dianions.;ChemInform;2010-08-20
3. Alkali Metal Reductions of Organic Molecules: Why Mediated Electron Transfer from Lithium Is Faster than Direct Reduction;Journal of the American Chemical Society;2008-09-17
4. Kinetics and thermodynamics of the Li/Li+ couple in tetrahydrofuran at low temperatures (195–295 K);Journal of Physical Organic Chemistry;2007
5. Five- and six-membered silicon–carbon heterocycles. Part 1. Synthetic methods for the construction of silacycles;Journal of the Chemical Society, Perkin Transactions 1;1998
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