898543-45-8Relevant articles and documents
Enantiopure encaged Verkade's superbases: Synthesis, chiroptical properties, and use as chiral derivatizing agent
Yang, Jian,Chatelet, Bastien,Hérault, Damien,Dufaud, Véronique,Robert, Vincent,Grass, Stéphane,Lacour, Jér?me,Vanthuyne, Nicolas,Jean, Marion,Albalat, Muriel,Dutasta, Jean-Pierre,Martinez, Alexandre
, p. 139 - 146 (2019/12/27)
Verkade's superbases, entrapped in the cavity of enantiopure hemicryptophane cages, have been synthesized with enantiomeric excess (ee) superior to 98%. Their absolute configuration has been determined by using electronic circular dichroism (ECD) spectros
Synthesis and in vitro antibacterial evaluation of novel 4-substituted 1-menthyl-1,2,3-triazoles
Khaligh, Pooneh,Salehi, Peyman,Bararjanian, Morteza,Aliahmadi, Atousa,Khavasi, Hamid Reza,Nejad-Ebrahimi, Samad
, p. 1589 - 1596 (2016/11/09)
Menthyl 1,4-disubstituted 1,2,3-triazole derivatives of hydroxybenzaldehydes, phenols and bile acids were synthesized via click chemistry. The novel synthesized compounds were evaluated for their in vitro antibacterial activity against Enterococcus faeciu
Enantioselective Rhodium(I)-Catalyzed Additions of Arylboronic Acids to N-1,2,3-Triazole-Isatin Derivatives: Accessing N-(1,2,3-Triazolmethyl)-3-hydroxy-3-aryloxindoles
Marques, Carolina S.,Burke, Anthony J.
, p. 3518 - 3526 (2016/11/29)
Oxindoles and triazoles are very privileged frameworks in medicinal chemistry, and thus for the first time we report a catalytic asymmetric route that affords hitherto unknown families of N-(1,2,3-triazolmethyl)-3-hydroxy-3-phenyloxindoles using cheap bio
