Photolability of Per-Arylated Butadienes: En Route to Dihydronaphthalenes
Author:
Affiliation:
1. Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg, Germany
2. Centre of Advanced Materials, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 225, 69120 Heidelberg, Germany
Funder
Landesgraduiertenförderung
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo502293q
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1. Simple Modifications for the Facile Preparation of 1,1,2,3,4,4‐Hexaaryl‐1,3‐butadienes;Helvetica Chimica Acta;2022-01-05
2. Aggregation‐Induced Emission of Triphenyl‐Substituted Tristyrylbenzenes;Chemistry – A European Journal;2019-07-15
3. Perarylation as a Strategy Toward Aggregation-Induced Emitters: Will They Ever Be Stable?;Principles and Applications of Aggregation-Induced Emission;2018-10-10
4. Aggregation-Induced Emission of Multiphenyl-Substituted 1,3-Butadiene Derivatives: Synthesis, Properties and Application;Chemistry - A European Journal;2018-08-13
5. [4 + 2] Annulation of Donor–Acceptor Cyclopropanes with Acetylenes Using 1,2-Zwitterionic Reactivity;The Journal of Organic Chemistry;2017-02-23
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