75677-03-1

Upstream product

• 1132981-62-4 ethyl 3-(2'-(benzyloxy)phenyl)propanoate 
• 91-64-5 coumarin 
• 1481-92-1 2-(3-hydroxypropyl)phenol 
• 152105-59-4 3-(2-benzyloxy-phenyl)-propan-1-ol 

Downstream Products

• 75676-89-0 6-(o-benzyloxyphenyl)-trans-3-hexen-2-one 
• 209120-22-9 [(E)-4-(2-Benzyloxy-phenyl)-1-fluoro-but-1-enyl]-phosphonic acid diethyl ester 
• 1030350-22-1 (2E)-5-(2-benzyloxy-phenyl)-pent-2-enoic acid ethyl ester 
• 75677-32-6 5H-r,7-(o-benzyloxyphenyl)-cis-4-bromo-cis-3-hydroxy-trans-3-methylheptan-5-olide 
• 75677-15-5 ethyl 7-(o-benzyloxyphenyl)-3-hydroxy-3-methyl-trans-4-heptenoate 
• 75677-49-5 5H-r,7-(o-benzyloxyphenyl)-cis-3-hydroxy-trans-3-methylheptan-5-olide 
• 209120-24-1 [(E)-1-Fluoro-4-(2-hydroxy-phenyl)-but-1-enyl]-phosphonic acid diethyl ester 
• 209120-23-0 [1-Fluoro-4-(2-hydroxy-phenyl)-butyl]-phosphonic acid diethyl ester 

Relevant academic research and scientific papers

Enantioselective synthesis of functionalized 1-benzoxepines by phenoxide ion mediated 7-endo-tet carbocyclization of cyclic sulfates

A new asymmetric synthesis of 2,3-disubstituted 1-benzoxepines is described. Key steps include Sharpless asymmetric dihydroxylation of trans-α,β-unsaturated esters and phenoxide ion mediated intramolecular 7-endo-tet carbocyclization of syn-2,3-dihydroxy ester derived cyclic sulfates. Wiley-VCH Verlag GmbH & Co. KGaA, 2009.

Application of phenolate ion mediated intramolecular epoxide ring opening in the enantioselective synthesis of functionalized 2,3-dihydrobenzofurans and 1-benzopyrans

The enantioselective synthesis of 2-isopropenyl-2,3-dihydrobenzofurans, 4-(2,3-dihydrobenzofuran-2-yl)-2-methylbut-3-en-2-ols, 2-hydroxymethyl chromans, and 4-chroman-2-yl-2-methylbut-3-en-2-ols has been achieved using Sharpless asymmetric epoxidation-der

β-Hydroxy-α-tosyloxy esters as chiral building blocks for the enantioselective synthesis of benzo-annulated oxa-heterocycles: scope and limitations

The enantioselective synthesis of benzo-annulated oxa-heterocycles 2,3-dihydrobenzofuran and 1-benzopyran derivatives is described using β-hydroxy-α-tosyloxy esters as chiral building blocks, which are easily accessible through the regioselective α-tosyla

Synthesis of arylalkylmonofluorophosphonates as myo-inositol monophosphatase ligands

Arylalkylmonofluorophosphonates were prepared by condensation of arylalkylaldehydes with the lithium salt of diethyl 1-fluore-1- (trimethylsilyl)-methylphosphonate. Reduction and hydrolysis sequences gave the final products. These compounds do not inhibit