38447-89-1Relevant articles and documents
Synthesis of novel C-2 substituted imidazoline derivatives having the norbornene/dibenzobarrelene skeletons
?apan, Irfan,Servi, Süleyman
supporting information, p. 131 - 142 (2018/10/26)
Novel imidazoline derivatives were synthesized from the norbornene and dibenzobarrelene skeletons which were obtained by the Diels-Alder reactions of anthracene and cyclopentadiene with the different dienophiles, such as fumaronitrile and fumaric acid. Synthesis of the C-2 substituted imidazolines was performed with high yields from various dinitriles and diacyl dichlorides.
Facile preparation of trans-2,3-bis(-tert-butylaminomethyl) norbornene
Wynne,Stalick
, p. 655 - 657 (2007/10/03)
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σ-bishomoaromatic heterocycles: Reactivity and synthesis of 3-oxatetracyclo[3.3.0.02,804,6]octane by photolysis at 185 nm
Klaerner, Frank-Gerrit,Dolz, Thomas,Uhlaender, Christoph,Yaslak, Salih
, p. 1385 - 1388 (2007/10/03)
The title compound 5 was produced by 185 nm photolysis of 8. The products of the 185 run photolysis can be rationalized by the assumption of the two diradical intermediates 16 and 17. At a temperature between 150 and 200°C 5 reacts with fumaronitrile 23 to give the adducts 7 and 26 in a ratio of about (5 : 1). The kinetic analysis of this reaction shows, that the adduct 7 is formed by 1,3 dipolar cycloaddition of intermediate carbonyl ylide 6.