314289-66-2

Upstream product

• 432036-78-7 5-benzyloxy-3,4-dihydronaphthalene 
• 211805-74-2 5-(benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-ol 
• 100-44-7 benzyl chloride 
• 90401-60-8 5-benzyloxy-1,2,3,4-tetrahydro-naphthalen-1-one 
• 28315-93-7 5-Hydroxy-1-tetralone 

Downstream Products

• 172936-73-1 (2R)-2-hydroxy-2-(N,N-diphenylcarbamoyloxymethyl)-5-ethoxycarbonylmethoxy-1,2,3,4-tetrahydronaphthalene 
• 314289-74-2 diphenylcarbamic acid ((2R)-2,5-dihydroxy-1,2,3,4-tetrahydronaphth-2-yl)methyl ester 
• 314289-73-1 diphenylcarbamic acid [((2R)-5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methyl]ester 
• 432036-86-7 methanesulfonic acid [((2S)-5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methyl]ester 
• 432036-85-6 C₁₉H₂₂O₅S 
• 432036-83-4 ((2R)-5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methanol 
• 439142-73-1 ((2S)-5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methanol 
• 432036-82-3 (-)-(1S,4R)-camphanic acid [((2R)-5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methyl]ester 
• 432036-84-5 (-)-(1S,4R)-camphanic acid [((2S)-5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methyl]ester 
• 432036-81-2 (-)-(1S,4R)-camphanic acid [(5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methyl]ester 
• 314289-69-5 (5-benzyloxy-2-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)methanol 
• 432036-80-1 5-benzyloxy-1,23,4-tetrahydrospiro[naphthalene-2,2'-oxirane] 
• 432036-79-8 5-benzyloxy-1,2,3,4-tetrahydro-2-oxonaphthalene 

Relevant academic research and scientific papers

Practical synthesis of PGI2 agonist: Resolution-inversion- recycle approach of its chiral intermediate

Practical synthesis of ((2R)-5-benzyloxy-2-hydroxy-1,2,3,4- tetrahydronaphth-2-yl)methanol ((R)-7b), a key chiral intermediate for the synthesis of the novel PGI2 agonist, (R)-[6-[(diphenylcarbamoyloxy) methyl]-6-hydroxy-5,6,7,8-tetrahydronapht

Practical and environmentally friendly epoxidation of olefins using Oxone

A practical and efficient epoxidation of aromatic olefins using Oxone in a two-phase system (ethyl acetate - water) is described. The reported method is suitable for large-scale synthesis and does not require phase transfer catalyst (PTC) or pH control.