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A peri ‐Cyclised Naphthalene Dimer: Synthesis and Properties of an Unusual Vilsmeier–Haack Product of 1,3,6,8‐Tetramethoxynaphthalene (Eur. J. Org. Chem. 26/2012)
Author(s) -
Pittelkow Michael,
Nielsen Christian B.,
BrockNannestad Theis,
SchauMagnussen Magnus,
Christensen Jørn B.
Publication year - 2012
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201290069
Subject(s) - formylation , dimer , chemistry , naphthalene , permission , cover (algebra) , schematic , product (mathematics) , medicinal chemistry , organic chemistry , engineering , catalysis , philosophy , mechanical engineering , geometry , mathematics , epistemology , electronic engineering
The cover picture shows the synthesis of a peri ‐cyclised naphthalene dimer formed by Vilsmeier–Haack formylation of 1,3,6,8‐tetramethoxynaphthalene. The cover features a schematic drawing of the H. C. Ørsted Institute at the University of Copenhagen where the research was performed. The stamp featuring H. C. Ørsted is reproduced with the permission of “Post & Tele Museum Danmark” and “Post Danmark”. Details are discussed in the article by M. Pittelkow, J. B. Christensen et al. on p. 4931 ff.