Aluminium‐organische Synthese im Bereich olefinischer Kohlenwasserstoffe
Publication type: Journal Article
Publication date: 1952-06-21
General Medicine
Abstract
Der Verlauf einer neuartigen Additionsreaktion von α-Olefinen an LiAlH4 bzw. AlH3 konnte aufgeklart werden. Uber die Additionsprodukte ist jetzt auch die C=C-Bindung in bestimmten Olefinen mit LiAlH4 bzw. AlH3 reduzierbar. Auch Aluminiumtrialkyle vermogen sich an Athylen oder α-Olefine zu addieren. Bei Temperaturen von etwa 200° C verandern Aluminiumtrialkyle Athylen und andere Olefine rein katalytisch unter Bildung hoherer Olefine durch Polymerisation, was der praparativen organischen Chemie und ihrer Technik neue Moglichkeiten eroffnet.
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Metrics
190
Total citations:
190
Citations from 2024:
4
(2.1%)
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GOST
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Ziegler K. Aluminium‐organische Synthese im Bereich olefinischer Kohlenwasserstoffe // Angewandte Chemie. 1952. Vol. 64. No. 12. pp. 323-329.
GOST all authors (up to 50)
Copy
Ziegler K. Aluminium‐organische Synthese im Bereich olefinischer Kohlenwasserstoffe // Angewandte Chemie. 1952. Vol. 64. No. 12. pp. 323-329.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1002/ange.19520641202
UR - https://doi.org/10.1002/ange.19520641202
TI - Aluminium‐organische Synthese im Bereich olefinischer Kohlenwasserstoffe
T2 - Angewandte Chemie
AU - Ziegler, Karl
PY - 1952
DA - 1952/06/21
PB - Wiley
SP - 323-329
IS - 12
VL - 64
SN - 0044-8249
SN - 1521-3757
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{1952_Ziegler,
author = {Karl Ziegler},
title = {Aluminium‐organische Synthese im Bereich olefinischer Kohlenwasserstoffe},
journal = {Angewandte Chemie},
year = {1952},
volume = {64},
publisher = {Wiley},
month = {jun},
url = {https://doi.org/10.1002/ange.19520641202},
number = {12},
pages = {323--329},
doi = {10.1002/ange.19520641202}
}
Cite this
MLA
Copy
Ziegler, Karl. “Aluminium‐organische Synthese im Bereich olefinischer Kohlenwasserstoffe.” Angewandte Chemie, vol. 64, no. 12, Jun. 1952, pp. 323-329. https://doi.org/10.1002/ange.19520641202.