Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemical synthesis. A route to this class of compound has been developed. Key steps include Noyori reduction (which establishes the stereochemistry of the product), ring-closing metathesis, and simple functional group conversions to provide a set of substituted 4-HCPs in either enantiomeric form
Catalytic enantioselective 1,4-additions and tandem 1,4-addition-aldol reactions of dialkylzinc reag...
The pseudoenantiomeric 4-O-Boc- and 4-OPMP-cyclopent-2-enones, readily available from hydroxymethyl...
The synthetic utilization of a chiral building block obtained by the enzymatic asymmetric hydrolysis...
Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemic...
Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chem...
Abstract This work describes the development of methods to access synthetically useful chiral diols ...
A new method for the synthesis of (R)-4-t-butyldimethylsiloxy-2-cyclopentenone (1, R = t-BuMe2-Si) h...
A brief, enantioselective synthesis of a hydroxymethyl-cis-1,3-cyclopentenediol building block is pr...
Prostaglandins (PGs) are medicinally interesting because of the wide variety of roles they play in t...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
The resolution by Lipase PS of rac-5 (from reduction of ketone 6, obtained from dicyclopentadiene wi...
An efficient entry into highly substituted cyclopentanones is presented based on functionalizing cyc...
Combining the desymmetrization of a prochiral bis-hydroxymethyl group with the epimerization of a ch...
The interest in five-membered ring molecules derives from their important application in many differ...
An asymmetric route for the synthesis of highly functionalized 2,3-epoxy-syn-1,4-cyclohexane diol de...
Catalytic enantioselective 1,4-additions and tandem 1,4-addition-aldol reactions of dialkylzinc reag...
The pseudoenantiomeric 4-O-Boc- and 4-OPMP-cyclopent-2-enones, readily available from hydroxymethyl...
The synthetic utilization of a chiral building block obtained by the enzymatic asymmetric hydrolysis...
Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemic...
Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chem...
Abstract This work describes the development of methods to access synthetically useful chiral diols ...
A new method for the synthesis of (R)-4-t-butyldimethylsiloxy-2-cyclopentenone (1, R = t-BuMe2-Si) h...
A brief, enantioselective synthesis of a hydroxymethyl-cis-1,3-cyclopentenediol building block is pr...
Prostaglandins (PGs) are medicinally interesting because of the wide variety of roles they play in t...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
The resolution by Lipase PS of rac-5 (from reduction of ketone 6, obtained from dicyclopentadiene wi...
An efficient entry into highly substituted cyclopentanones is presented based on functionalizing cyc...
Combining the desymmetrization of a prochiral bis-hydroxymethyl group with the epimerization of a ch...
The interest in five-membered ring molecules derives from their important application in many differ...
An asymmetric route for the synthesis of highly functionalized 2,3-epoxy-syn-1,4-cyclohexane diol de...
Catalytic enantioselective 1,4-additions and tandem 1,4-addition-aldol reactions of dialkylzinc reag...
The pseudoenantiomeric 4-O-Boc- and 4-OPMP-cyclopent-2-enones, readily available from hydroxymethyl...
The synthetic utilization of a chiral building block obtained by the enzymatic asymmetric hydrolysis...