16516-83-9

Upstream product

• 106-95-6 allyl bromide 
• 95-95-4 2,4,5-trichlorophenol 

Downstream Products

• 54582-85-3 2-allyl-3.4.6-trichlorophenol 
• 153617-05-1 3-Allyl-1,2,5-trichloro-4-methoxy-benzene 
• 286474-98-4 (4S,6S)-4-Allyl-2,2-dimethyl-6-(2,4,5-trichloro-phenoxymethyl)-[1,3]dioxane 
• 286474-97-3 (2S,4S)-1-(2,4,5-Trichloro-phenoxy)-hept-6-ene-2,4-diol 
• 286474-95-1 (S)-1-(2,4,5-Trichloro-phenoxy)-pent-4-en-2-ol 
• 286474-96-2 (S)-3-Hydroxy-4-(2,4,5-trichloro-phenoxy)-butyraldehyde 
• 123224-54-4 (2,4,5-trichloro-phenoxy)-acetaldehyde 

Relevant academic research and scientific papers

Addition of nitrile oxides to aryl allyl ethers

3,5-Disubstituted isoxazolines with an aryloxymethyl group in position 5 have been synthesized. The [2+3] cycloaddition reaction of benzonitrile oxide to a 5-chlorosalicylic acid derivative containing two allyl groups occurs to give a compound with an oxa

Enantioselective allyltitanation. Application to the synthesis of lactone units related to compactin and mevinolin

The enantioselective convergent synthesis of two different models of the lactone units of compactin and mevinolin was achieved using two consecutive enantioselective allyltitanations of aldehydes.

Phase-transfer catalyzed nucleophilic addition of arylalkanenitrile carbanions to substituted propenylarenes

Phenylacetonitrile and 2-phenylalkanenitriles react under phase transfer catalysis conditions with 2-propenylanisoles containing electron-withdrawing substituents (or their corresponding precursors, 2-allylanisoles) via the Michael addition pathway to give substituted 4-aryl-2-phenylbutyronitriles.