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Propellanes V. [3.3.1] Propellane

✍ Scribed by Philip Warner; Richard LaRose; Thomas Schleis


Publisher
Elsevier Science
Year
1974
Tongue
French
Weight
181 KB
Volume
15
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES


Propellanes. Part LXXVIII. Preparation o
✍ Olga Weinberg; Philip Knowles; David Ginsburg 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 German ⚖ 269 KB

## Abstract 3,7,10‐Tribenzyl‐3,7,10‐triaza[3.3.3]propellane (**4a**), 3,7‐dibenzyl‐10‐phenyl‐3,7,10‐triaza[3.3.3]propellane (**4c**), 3,7‐dibenzyl‐10‐(__p__‐tolyl)‐3,7,10‐triaza[3.3.3]propellane (**4b**), and 3‐oxa‐7,10‐diaza[3.3.3]propellane (**6**) have been prepared.

[3.3.1]-propellane-2,8-dione
✍ I. David Reingold; James Drake 📂 Article 📅 1989 🏛 Elsevier Science 🌐 French ⚖ 126 KB

The title compound was prepared by transammlar addition of a carbene to an exocyclic double bond. Rhodium acetate catalyzed decomposition of 2-diazo-&methylene-1,3-cyclooctanedione gave 1 quantitatively. We wish to report the first synthesis of the title compound, 1, and a new approach to propellan

Propellanes. Part LXX. The oximes of [4.
✍ Soundararajan Bhanumati; Pnina Ashkenazi; David Ginsburg 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 German ⚖ 72 KB 👁 1 views

## Abstract The mono‐oxime and dioxime of the title compound have been prepared.

Propellanes. Part LXXX. Baeyer-Villiger
✍ Pnina Ashkenazi; Moshe Kapon; Umberto Piantini; Wolfgang Von Philipsborn; David 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 German ⚖ 247 KB 👁 1 views

## Abstract Oxidation of the title compound with __m__‐chloroperbenzoic acid affords a keto‐lactone, two bis‐lactones and a bis‐spirolactone, in varying amounts depending upon the reaction conditions. The structures were established by means of X‐ray diffraction, ^1^H‐ and ^13^C‐NMR spectroscopy.