✦ LIBER ✦

Tetracyclo[5.2.0.01,6.02,7]nonane, A [2.1.1]propellane derivative as a reaction intermediate

✍ Scribed by Jan Morf; Günter Szeimies

Book ID: 104219290
Publisher: Elsevier Science
Year: 1986
Tongue: French
Weight: 191 KB
Volume: 27
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)85211-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Tetracyclo[5.1.0.01,6.02,7]octane: some

Tetracyclo[5.1.0.01,6.02,7]octane: some unexpected addition reactions and a new synthesis

✍ Johannes Belzner; Günter Szeimies 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 217 KB

Reaction of 1,6-dihalopentacyclo[5.2.0.0

Reaction of 1,6-dihalopentacyclo[5.2.0.02,6.03,9.05,8]Nonanes with tert-butyllithium: Is 1,6-dehydrohomocubane involved as a reactive intermediate?

✍ Jörg Schäfer; Günter Szeimies 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 319 KB

The Central Propellane Bond as Polymeriz

The Central Propellane Bond as Polymerizable CC Single Bond: Poly(tricyclo[4.2.0.02,7]octane-1,7-diyl)—a “Poly([1.1.1]propellane)”

✍ Dr. Arnulf-Dieter Schlüter 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 English ⚖ 335 KB 👁 1 views

Reaction of 1-bromo-7-chloropentacyclo[5

Reaction of 1-bromo-7-chloropentacyclo[5.2.0.02,6.03,9.05, 8]nonane with tert-bithyllithium: Evidence for 1(7)-homocubene

✍ Jörg Schäfer; Günter Szeimies 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 97 KB

Computational note on a G4 theoretical s

Computational note on a G4 theoretical study of the small-ring geminanes tricyclo[3.1.1.01,4]heptane, tetracyclo[3.1.1.12,4.01,5]octane, and tetracyclo[3.2.12,4.02,5]nonane

✍ Sierra Rayne; Kaya Forest 📂 Article 📅 2011 🏛 Elsevier 🌐 English ⚖ 158 KB

Computational note on a G4 theoretical study of the small-ring geminanes tricyclo[3.1.1.0 1,4 ]heptane, tetracyclo[3.1.1.1 2,4 .0 1,5 ]octane, and tetracyclo[3.2.1 2,4 .0 2,5 ]nonane

Reactions of 1,3,5-Tri-tert-butylcyclope

Reactions of 1,3,5-Tri-tert-butylcyclopentadiene formation of a tetracyclo[5.2.1.02,6.03,10]deca-4,8-diene

✍ Dehmlow, Eckehard V. ;Bollmann, Christof 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 332 KB

Title compound 1 is sterically shielded to such an extent that many "normal" reactions cannot occur. It is possible, however, to prepare the carboxylic acid 2, its acyl chloride 3 and the oxidation product 4. Furthermore, halogen substitutions to yield 5 and 6 and trialkylstannations to give 8a, b c