Neue [m.n]Cyclophane durch sukzessive Ketonpyrolyse
Author:
Affiliation:
1. Institut für Organische Chemie und Biochemie der Universität Bonn, Gerhard‐Domagk‐Straße 1, 53121 Bonn
2. Anorganisch‐chemisches Institut der Universität Bonn, Gerhard‐Domagk‐Straße 1, 53121 Bonn
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19931261122
Reference32 articles.
1. Selektive Ketonpyrolyse: Neue Synthesemethode für mono- und polycyclische Kohlenwasserstoffe
2. Selective Ketone Pyrolysis: New Synthetic Method for Mono- and Polycyclic Hydrocarbons
3. Ketonpyrolyse: Darstellung und Röntgen‐Kristallstruktur eines Oxa[3.2.1]cyclophans
4. Selektive Ketonpyrolyse: Neue Beispiele
5. A facile synthesis of [3ncyclophanes, in which aromatic rings are connected with -CH2CO-CH2- bridges
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4. Bis-Quinolinium Cyclophanes: 8,14-Diaza-1,7(1,4)-diquinolinacyclotetradecaphane (UCL 1848), a Highly Potent and Selective, Nonpeptidic Blocker of the Apamin-Sensitive Ca2+-Activated K+ Channel;Journal of Medicinal Chemistry;2000-08-31
5. Synthetic applications of flash vacuum pyrolysis;Contemporary Organic Synthesis;1996
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