58876-96-3

Upstream product

• 870-63-3 prenyl bromide 
• 1193-00-6 sodium 4-chlorophenolate 
• 106-48-9 4-chloro-phenol 
• 115-18-4 2-methyl-3-buten-2-ol 

Downstream Products

• 59516-92-6 4-chloro-2-(3-methylbut-2-en-1-yl)phenol 
• 86558-41-0 3-chloro-2-chloromethyl-4-(4-chlorophenoxy)-1-butene 
• 86558-42-1 3-chloro-4-(4-chlorophenoxy)-2-(phenylsulfonylmethyl)-1-butene 
• 86558-43-2 3-chloro-4-(4-chlorophenoxy)-2-(phenylthiomethyl)-1-butene 
• 84369-87-9 2-(phenylthiylmethyl)-1,3-butadiene 
• 50465-44-6 2-<(phenylsulphonyl)methyl>-1,3-butadiene 

Relevant academic research and scientific papers

A dehydrogenative diels-alder reaction of prenyl derivatives with 2,3-dichloro-5,6-dicyanobenzoquinone

An efficient dehydrogenative Diels-Alder (DHDA) reaction of prenyl derivatives with 2,3-dichloro-5,6-dicyanobenzoquinone (DDQ) has been developed under mild conditions, leading to a series of cyclohexene derivatives with good to excellent yields and excellent diastereoselectivity.

Regioselectivity in the ene reaction of singlet oxygen with ortho-prenylphenol derivatives

The ene reaction of singlet oxygen with prenylated dihydroxyacetophenones led to the 2-hydroperoxy-3-methylbut-3-enyl derivatives as the major product. This original regioselectivity outlined a new effect, in competition with the previously established la

First total synthesis of artepillin C established by o,o′-diprenylation of p-halophenols in water

We have demonstrated that prenylation of phalophenols was dependent on the solvent effect and succeeded in o,o′-diprenylation of p-halophenols in water. Following the Mizoroki-Heck coupling of the diprenyl-piodophenol 3c with methyl acrylate and then hydr

A new synthesis of allyl ethers via allyldialkyltelluronium salts

Allyldialkyltelluronium bromides were treated with phenols in the presence of NaOH at room temperature, readily giving allyl aromatic ethers in excellent yields. This procedure represents an efficient means for synthesis of allyl aromatic ethers.

5-Nitropyrimidines

Novel pteridines of formula (I), SPC1 wherein R is an optionally substituted phenoxyalkyl group, and R1 and R2 are the same or different and each is a lower alkyl group or R1 and R2, together with the carbon atom in the pteridine ring structure, form a spirocycloalkyl ring system having 4 to 6 carbon atoms outside the pteridine ring structure, And their method of preparation. The above compounds have bacteriostatic activity.