76561-85-8Relevant articles and documents
Synthesis and biological effects evaluation of benzoconduritols C and D from oxabenzonorbornadiene
?ol Ayvaz, Melek,?ahin, Ertan,Kelebekli, Latif,Y?lmaz, Fatma Zehra
, (2021/10/25)
The effective synthesis of benzoconduritols C and D is reported. Oxidation of oxabenzonorbornadiene followed by acetylation with Ac2O/pyridine or AcCl/CH2Cl2 gave the corresponding exo-diacetate compound stereoselectively.
Chemoenzymatic synthesis of conduritol analogues
Orsini, Fulvia,Sello, Guido,Bernasconi, Silvana,Fallacara, Gianfranco
, p. 9253 - 9255 (2007/10/03)
Several conduritol and conduramine analogues have been synthesized from β-substituted naphthalenes via a chemoenzymatic approach, in a high regio- and stereocontrolled way. Several conduritol and conduramine analogues have been synthesized from β-substituted naphthalenes via a chemoenzymatic approach, in a high regio- and stereocontrolled way.
Synthesis and biological evaluation of conduritol and conduramine analogs
Desjardins, Michel,Lallemand, Marie-Christine,Freeman, Stanley,Hudlicky, Tomas,Abboud, Khalil A.
, p. 621 - 628 (2007/10/03)
A number of dimeric conduritol and conduramine analogs have been synthesized from naphthalene via a combination of enzymatic and chemical methods to give oxygenated derivatives with high stereo- and regiocontrol in few steps. These compounds have been tested for enzymatic inhibition against common glycosidases.