1,3-Diazaanthracenes: photochemical [4π+4π] cycloadditions with cyclopenta-1,3-diene and dimerisations to new bis-pyrimidines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. A new building block technique based on cycloaddition chemistry for the regiospecific linking of alicyclic sub-units as a route to large, custom-functionalised structures
2. 2,4-Dimethoxy-1,3-diazaanthracene, a Diels-Alder Diene for the Preparation of Polyalicyclic Structures Functionalised with Uracil Subunits
3. Dimerization Reactions in Sunlight.
4. Photoadditionen von Dibenz[ a , c ]‐ und Dibenz[ a , h ]anthracen an Cyclopentadien
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1. Photochromic benzo[g]quinoxalines;Canadian Journal of Chemistry;2011-02
2. ChemInform Abstract: Building BLOCKs in Synthesis. Part 9. 1,3-Diazaanthracenes: Photochemical [4π + 4π] Cycloadditions with Cyclopenta-1,3-diene and Dimerizations to New Bispyrimidines.;ChemInform;2010-06-19
3. The reversible [4+4] photocycloaddition of acridizinium derivatives;Journal of Photochemistry and Photobiology A: Chemistry;2008-11
4. Use of a 9,10-Dihydrofulvalene Pincer Cycloadduct as a Cornerstone for Molecular Architecture;Australian Journal of Chemistry;2006
5. The Synthesis of Geometric Variants of Rigidly-Linked Uracil-{Spacer}-Uracil and Uracil-{Spacer}-Effector Molecules Using Block Assembly Methods;Nucleosides and Nucleotides;1999-11
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