✦ LIBER ✦

Preparation and Properties of 1,2-Diethylidene-cyclobutane

✍ Scribed by Priv.-Doz. Dr. P. Heimbach; Dipl.-Chem. R. Schimpf

Publisher: John Wiley and Sons
Year: 1969
Tongue: English
Weight: 285 KB
Volume: 8
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.196902061

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Preparation and Properties of Imidazole-

Preparation and Properties of Imidazole-2-carbaldehyde

✍ Prof. H. Schubert; H.-D. Rudorf 📂 Article 📅 1966 🏛 John Wiley and Sons 🌐 English ⚖ 198 KB 👁 1 views

Preparation and Properties of AuTe2I

✍ Prof. Dr. A. Rabenau; Dr. H. Rau; G. Rosenstein 📂 Article 📅 1969 🏛 John Wiley and Sons 🌐 English ⚖ 346 KB 👁 2 views

Preparation and properties of EPDM/TiO2

Preparation and properties of EPDM/TiO2 composites

✍ Shan Haitao; Cui Juqing; Zhang Qiang; Zhuang Wei; He Qihui; Hu Baixing; Shen Jia 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 205 KB 👁 1 views

Preparation and application of fluorocar

Preparation and application of fluorocarbon polymer/SiO2 hybrid materials, part 1: Preparation and properties of hybrid materials

✍ Jen-Taut Yeh; Chin-Lai Chen; Kuo-Shien Huang 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 426 KB 👁 2 views

Preparation and Properties of Stelladion

Preparation and Properties of Stelladiones

✍ Rolf Gleiter; Bettina Gaa; Christoph Sigwart; Holger Lange; Oliver Borzyk; Frank 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 453 KB 👁 1 views

2,4-dione (2,4-stelladione, 3), tri-toelectron spectra of 3, 5, and 4-methylenetricyclo-[3.3.0.0 3,7 ]octan-2-one (9) were recorded and interpreted on cyclo[3.3.0.0 3,7 ]octane-2,6-dione (2,6-stelladione, 4), and 2oxotricyclo[3.3.0.0 3,7 ]octane-6-thione (5) were synthesized. the basis of quantum-m

Preparation and properties of polycarbod

Preparation and properties of polycarbodiimides

✍ L. M. Alberino; W. J. Farrissey JR.; A. A. R. Sayigh 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 464 KB

## Abstract A series of polycarbodiimides was prepared from isocyanates using 1‐phenyl‐3‐methyl‐2‐phospholene‐1 oxide as catalyst. The molecular weight of the series was varied by employing controlled amounts of phenyl isocyanate as a terminating agent. The resultant polymers showed improved proces