123027-96-3

Upstream product

• 17763-71-2 4-carbomethoxyphenyl triflate 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 99-42-3 methyl (4-hydroxy-3-nitro)benzoate 

Downstream Products

• 123027-97-4 2-amino-4-carbomethoxyphenyl trifluoromethanesulfonate 
• 39180-36-4 methyl 2-nitro[1,1'-biphenyl]-4-carboxylate 
• 815632-40-7 methyl 9-phenyl-9H-carbazole-2-carboxylate 
• 1033997-01-1 methyl 4-cyano-3-nitrobenzoate 
• 123027-98-5 N-acetyl-5-carbomethoxy-2-<(trifluoromethyl)sulfonyl>aniline 
• 123028-08-0 N-acetyl-2-(phenylethynyl)-5-carbomethoxyaniline 
• 123028-29-5 methyl 1-acetyl-2-phenyl-1H-indole-6-carboxylate 
• 123028-09-1 N-acetyl-2-<(trimethylsilyl)ethynyl>-5-carbomethoxyaniline 
• 123028-07-9 N-acetyl-2-hexyn-1-yl-5-carbomethoxyaniline 
• 123028-06-8 N-acetyl-2-(3-methylbutyn-1-yl)-5-carbomethoxyaniline 
• 123028-05-7 N-acetyl-2-pentyn-1-yl-5-carbomethoxyaniline 
• 50820-65-0 indole-6-carboxylic acid methyl ester 
• 26000-33-9 methyl 9H-carbazole-2-carboxylate 
• 126759-36-2 methyl 4-ethenyl-3-nitrobenzoate 

Relevant academic research and scientific papers

Stille and suzuki cross coupling reactions of o-nitrophenyl triflates: A versatile route to a variety of heterocycles

The cross coupling reactions of selected o-nitrophenyl triflates with arylstannane and arylboron substrates are reported. The resultant 2-nitrobiphenyls provide ready access to a variety of substituted heterocycles.

INSECTICIDAL COMPOUNDS

A compound of formula (I): wherein A1, A2, A3, A4, R1, R2, G1, G2, Q1 and Q2 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore

O-nitrophenyltriflates in quinoline synthesis : Easy access to a streptonigrin synthon

An efficient route to a wide range of 2-hydroxyquinolines from o-nitrophenyltriflates via a Heck reaction is reported, with emphasis on the preparation of a synthetic equivalent of the streptonigrin AB ring system.