1,3‐Anionische Cycloadditionen, XIII. endo‐exo ‐Isomere Cycloaddukte aus trans , trans ‐1,3‐Diphenyl‐2‐azaallyllithium und Acenaphthylen
Author:
Affiliation:
1. Organisch‐Chemisches Institut der Universität Münster, Orléans‐Ring 23, D‐4400 Münster
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19771100225
Reference23 articles.
1. 1,3-Anionische Cycloadditionen von 2-(N,N-Diisopropylcarbamoyl)-allyllithium mit Zweistufenmechanismus
2. 1,3-Anionic Cycloadditions of 2-(N,N-Diisopropylcar-bamoyl) allyllithium with a Two-Step Mechanism
3. 1,3-Anionische Cycloadditionen von Organolithiumverbindungen; eine erste Übersicht
4. 1,3-Anionic Cycloadditions of Organolithium Compounds: An Initial Survey. New synthetic methods (4)
5. E.Köppelmann Dissertation Univ. Münster1971.
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