Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kou P. Kawahara"'
Publikováno v:
Chemical Communications. 59:1157-1160
We developed a sulfur-embedding annulative π-extension (thia-APEX) reaction that could construct a sulfur-embedding cationic hexagonal aromatic ring, thiopyrylium, onto unfunctionalized aromatics in one step. The key of thia-APEX is the use of
One-step synthesis of polycyclic thianthrenes from unfunctionalized aromatics by thia-APEX reactions
Publikováno v:
Organic Chemistry Frontiers. 10:1880-1889
In this paper, thia-APEX reactions affording π-extended thianthrene derivatives from unfunctionalized aromatics are described.
Publikováno v:
Journal of the American Chemical Society. 145:658-666
Among a large variety of organic semiconducting materials, rubrene (5,6,11,12-tetraphenyltetracene) represents one of the most prominent molecular entities mainly because of its unusually high carrier mobility. Toward finding superior rubrene-based o
Publikováno v:
Angewandte Chemie (International ed. in English). 59(16)
Nitrogen-containing polycyclic aromatic compounds (N-PACs) are an important class of compounds in materials science. Reported here is a new aza-annulative π-extension (aza-APEX) reaction that allows rapid access to a range of N-PACs in 11-84 % yield