6153-89-5

Usage

InChI:InChI=1/C18H12N2/c1-2-6-13(7-3-1)16-12-14-8-4-10-19-17(14)18-15(16)9-5-11-20-18/h1-12H

Upstream product

• 68527-71-9 6-phenyl-8-aminoquinoline 
• 5393-46-4 4-acetamido-3-nitro-biphenyl 
• 1028424-68-1 (Z)-2-bromo-3-(2-(2-bromopyridin-3-yl)-2-phenylvinyl)pyridine 
• 40000-20-2 5-bromo-1,10-phenanthroline 
• 98-80-6 phenylboronic acid 
• 68527-70-8 6-phenyl-8-nitroquinoline 

Downstream Products

• 81655-93-8 C₅₄H₃₆N₆Rh⁽³⁺⁾ 
• 105061-76-5 Cu(C₁₂H₇N₂(C₆H₅))(P(C₆H₅)3)2⁽¹⁺⁾*BF₄^(1-)=(Cu(C₁₂H₇N₂(C₆H₅))(P(C₆H₅)3)2)BF₄ 
• 87655-72-9 W(CO)4(5-phenyl-1,10-phenanthroline) 
• 101056-26-2 Mo(CO)4(5-phenyl-1,10-phenanthroline) 
• 101056-24-0 Cr(CO)4(5-phenyl-1,10-phenanthroline) 
• 229622-24-6 [Cu(5-phenyl-1,10-phenanthroline)(acetylacetonate)]NO₃ 
• 229622-32-6 [Cu(5-phenyl-1,10-phenanthroline)(salicylaldehydate)]NO₃ 
• 265328-49-2 [Eu(III)(NO₃)3(5-phenyl-1,10-phenanthroline)2] 

Relevant academic research and scientific papers

Synthesis of 6-phenylbenzo[h]quinolinesviaphotoinduced dehydrogenative annulation of (E)-2-phenyl-3-styrylpyridines

A concise and environmentally friendly protocol was developed for the synthesis of 6-phenylbenzo[h]quinolines. 6-Phenylbenzo[h]quinolines were obtained in good yieldsviairradiation of (E)-2-phenyl-3-styrylpyridines with a 254 nm UV light (64 W) in EtOH under an argon atmosphere in the presence of TFA. The reaction is a dehydrogenative annulation reaction that proceeds through 6π-electrocyclization, a [1,5]-H shift, 1,3-enamine tautomerization, and elimination of a hydrogen molecule to afford 6-phenylbenzo[h]quinolines. The described protocol not only avoids the usage of a transition metal catalyst and an oxidant but also has the advantages of high atom efficiency and mild reaction conditions.

With the antibacterial activity of the substituted 2 - amido - 1, 10 - eurepium (by machine translation)

The invention relates to a compound of formula I is shown of a substituted 2 - amido - 1, 10 - eurepium antibacterial compound or its physiologically acceptable salt and their method of preparation, also relates to a pharmaceutical composition comprising said compound. Wherein each substituent defined as stated in claims. (by machine translation)

Synthesis of stereodefined 1-aryl(heteroaryl) substituted 1,2-bis(2-bromopyridin-3-yl)ethenes by selective tandem Suzuki-Miyaura cross-coupling reactions

A protocol for the synthesis of stereodefined 1-aryl(heteroaryl) substituted 1,2-bis(2-bromopyridin-3-yl)ethenes by tandem Suzuki-Miyaura cross-coupling reactions and an example of convention into 5-phenyl-1,10-phenanthroline are described.

Production method of a cross-coupling compound from an alkyl halide and an organoboron compound

There is provided a method for producing a coupling compound of formula (1):(Y-)(n-1)R1-R2-(R1)(n'-1) wherein R1, R2 n and n' are as defined below, Y is R2 or X as defined below, which method comprises reactinganorganichalogen compound of formula (2):n' (R1X1n) wherein X1 represents a bromine or iodine, R1 represents a substituted or unsubstituted, linear, branched or cyclic hydrocarbon group of which α and β carbon atoms in relation to X1 are sp3 carbon atoms, n and n' each independently represent an integer of 1 or 2, and provided that n and n' do not simultaneously represent 2, with an organic boron compound of formula (3):m{R2(BX22)n'} wherein R2 represents a substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl or substituted or unsubstituted alkenyl group and the boron atom is bonded with an sp2 carbon atom thereof, X2 represents a hydroxyl or alkoxy group, n' is as defined above, m represents an integer of 1 or 2, and m is not more than n, in the presence of a catalyst comprising a) a nickel compound, and ???b) b-1) a compound of formula (i): ???or ???b-2) a compound of formula (ii):