27258-80-6

Upstream product

• 536-74-3 phenylacetylene 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 36229-69-3 1-[2-(1-hydroxy-3-phenylprop-2-ynyl)phenyl]-3-phenylprop-2-yn-1-ol 

Downstream Products

• 31273-03-7 2-Diethylamino-3-methyl-1,4-diphenyl-anthraquinone 
• 28051-16-3 1,2,4-triphenylanthraquinone 
• 31273-01-5 1,3,4-Triphenyl-2-brom-anthrachinon 
• 27258-81-7 1,2,3,4-Tetraphenyl-9,10-anthrachinon 
• 31273-02-6 2-Ethoxy-1,4-diphenyl-anthraquinone 
• 31352-92-8 2-Isopropenyl-1,4-diphenyl-anthraquinone 
• 26252-51-7 1,3-diphenyl-naphtho[2,3-c]thiophene-4,9-dione 
• 705964-65-4 [((C₆H₅)CC(C(O)C₆H₄C(O))CC(C₆H₅))RuCl(C₅(CH₃)5)]*CHCl₃ 
• 53271-91-3 1,2,4-Triphenyl-3-[2-(3-phenyl-propynoyl)-benzoyl]-anthraquinone 
• 41991-69-9 (6Z,14Z)-6,7,14,15-Tetraphenyl-cycloocta[1,2-b;5,6-b']dinaphthalene-5,8,13,16-tetraone 
• 31272-96-5 2-Benzoyl-1,3,4-triphenyl-9,10-anthrachinon 
• 28051-17-4 1.4-Diphenyl-anthrachinon-2.3-dicarbonsaeure-methylester 
• 36297-64-0 C₆₅H₃₈O₅ 
• 31273-00-4 1,2,4-Triphenyl-3-(3-phenyl-propynoyl)-anthraquinone 

Relevant academic research and scientific papers

1,3-Dialkynyl- and 1,3-dialkenylisobenzofurans: New π-extended congeners prepared by double nucleophilic addition of alkynyllithiums to o-phthalaldehyde

Efficient synthetic route to 1,3-dialkynyl- and 1,3-dialkenylisobenzofurans, new π-extended congeners of isobenzofurans, was reported. A three-step protocol including double nucleophilic additions of alkynyllithiums to o-phthalaldehyde and selective oxida

Recursive Anion-Triggered Tandem Reactions of ortho-Bis-ynones: Tunable Synthesis of 1-Indenones and Cyclopenta[ a]inden-8(2 H)-ones

Recursive anion-mediated activation of o-bis-ynones sets off a Michael addition-aldol reaction-dehydrative rearrangement cascade, leading to the one-pot synthesis of 1-indenones via orthogonal interplay between the two ortho-ynone moieties. Repeating the recursive anion engagement with the 1-indenones unfolded access to a functionally embellished cyclopenta[a]inden-8(2H)-one core and its spiroannulated analogues either directly or stepwise through tandem 1,6-Michael-type addition-6πelectrocyclization and an in situ oxidation sequence.

Catalytic [2 + 2 + 2] and thermal [4 + 2] cycloaddition of 1,2-bis(arylpropiolyl)benzenes

We have determined that a cationic rhodium(I)/Segphos complex catalyzes an enantio- and diastereoselective intermolecular [2 + 2 + 2] cycloaddition of 1,2-bis(arylpropiolyl)benzenes with various monoalkynes at room temperature to give axially chiral 1,4-t