153684-50-5Relevant academic research and scientific papers
NOVEL COMPOUND AND ORGANIC ELECTROLUMINESCENT ELEMENT PRODUCED USING SAME
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Paragraph 0325-0327, (2016/11/07)
A compound represented by the following formula (1): wherein in the formula, L1 is a single bond or a linking group, A is a group represented by the following formula (A), B is a group represented by the following formula (B), m is an integer of 1 to 3, and n is an integer of 1 to 4.
Tetrazoles: XLVIII. 3H-naphtho[2,1-e]-and 3H-naphtho[1,2-e][1,2,4] triazepines from 5-aryltetrazoles. Physical and chemical properties
Nikulin,Artamonova,Koldobskii
, p. 444 - 449 (2007/10/03)
Thermolysis of N-imidoyltetrazoles generated under conditions of phase-transfer catalysis from 5-aryltetrazoles and N-(2-naphthyl)benzimidoyl chloride yields 3H-naphtho[2,1-e][1,2,4]triazepines, and acid hydrolysis of the latter leads to formation of 3-ar
Synthesis of Benzo-Fused Benzodiazepines Employed as Probes of the Agonist Pharmacophore of Benzodiazepine Receptors
Zhang, Weijiang,Koehler, Konrad F.,Harris, Bradford,Skolnick, Phil,Cook, James M.
, p. 745 - 757 (2007/10/02)
The synthesis and in vitro evaluation of benzo-fused benzodiazepines 1-6 are described.These "molecular yardsticks" were employed to probe the spatial dimensions of the lipophilic pocket L2 in the benzodiazepine receptor (BzR) cleft and to dete
The Regiospecific Synthesis Of Ortho Aminonaphthophenones Via The Addition Of Carbanions To Naphthoxazin-4-Ones
Zhang, Weijiang,Liu, Ruiyan,Cook, James M.
, p. 2229 - 2236 (2007/10/02)
The conversion of nitronaphthalenes (see 4a and 4b) into the corresponding ortho aminonaphthylnitriles (5a and 5b) via the process of Tomioka, when combined with the addition of carbanions to the intermediate naphthoxazin-4-ones, provided a route to ortho aminonaphthophenones (7a) and (7b).These key intermediates were employed to synthesize the benzfused 2'-fluoro-1,4-benzodiazepines (1-3).
