5653-33-8

Upstream product

• 486-25-9 9-fluorenone 
• 98-86-2 acetophenone 
• 7049-31-2 9-fluorenone thioketal 
• 70-11-1 α-bromoacetophenone 
• 89003-97-4 3-(2-iodophenyl)-1-phenylprop-2-en-1-one 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 89003-97-4 (E)-3-(2-iodophenyl)-1-phenylprop-2-en-1-one 
• 73249-91-9 9,9-bis(benzoylmethyl)fluorene 
• 55526-36-8 3,3-(biphenyl-2,2'-diyl)-1-bromo-1-phenylallene 
• 25164-43-6 9-isocyano-9H-fluorene 
• 532-27-4 1-chloroacetophenone 
• 53156-46-0 9-(N,N-dimethylamino)fluorene 
• 857566-41-7 2-(9H-fluoren-9-yl)-1-phenylethan-1-one 
• 117745-96-7 9-phenylethynylfluoren-9-ol 

Downstream Products

• 1095033-74-1 C₂₉H₂₄O₃ 
• 1095033-72-9 C₂₇H₂₀O₃ 
• 75115-10-5 4'-bromo-3'-phenylspiro<9H-fluorene-9,5'(4'H)isoxazole> 
• 75115-14-9 3-phenylphenantro<9,10-d>isoxazole 
• 10423-18-4 2-phenylspiro[cyclopropane-1,9'-fluorene] 
• 23921-41-7 2-(9'-fluorenylidene)acetophenone oxime 
• 29416-91-9 phenyl-(2'-phenyl-4',5'-dihydro-spiro[fluorene-9,6'-[1,3]oxazin]-5'-yl)-methanone 
• 857566-41-7 2-(9H-fluoren-9-yl)-1-phenylethan-1-one 
• 143007-31-2 2-(9-Fluorenyl)-1-phenylethanol 

Relevant academic research and scientific papers

Dithioacetal as a 1,1-zwitterion synthon. Synthesis of functionalized alkenes by the coupling of benzylic dithioacetals with another 1,1-zwitterion synthon

Reaction of a dithioacetal sequentially with BuLi and alkyl bromide having an electron withdrawing substituent at the α-position followed by treatment with neutral alumina gives the corresponding olefination product in moderate to good yields.

Synthesis of 9-fluorenylidenes and 9,10-phenanthrenes through palladium-catalyzed aryne annulation by o-halostyrenes and o-halo allylic benzenes

(Chemical Equation Presented) A number of functionally substituted 9-fluorenylidenes and 9,10-phenanthrenes have been synthesized from substituted o-halostyrenes and o-halo allylic benzenes respectively in good yields by the palladium-catalyzed annulation

Palladium-catalyzed synthesis of 9-fluorenylidenes through aryne annulation

The palladium-catalyzed annulation of arynes by substituted o-halostyrenes produces substituted 9-fluorenylidenes in good yields. This methodology provides this important carbocyclic ring system in a single step, which involves the generation of two new c

Reinvestigation on Thermal Cycloaddition of 1-Aryl-2-(9-fluorenylidene)-1-haloethylenes

The thermal treatment of 1-bromo-2-(9-fluorenylidene)-1-phenylethylene afforded three different types of cycloaddition products.The 1-tolyl homolog showed similar trends, but the chloro analog gave only two types.These results suggest that reactions

β-Elimination of the Isonitrile Group in Alkylation Reactions of C-H Acids Activated by the Isonitrile Function

During phase-transfer alkylation of the isonitriles R1R2CHNC with X-CH2-Y, where X is a leaving group and Y an electron withdrawing group, some of the alkylation products undergo β-elimination of the isonitrile function to yield R1R2C=CHY.