88958-64-9Relevant articles and documents
(S,S,S)-Perhydroindolic acid: efficient catalyst for direct asymmetric aldol reaction from aromatic aldehydes
Tang, Xiaoping,Liegault, Benoit,Renaud, Jean-Luc,Bruneau, Christian
, p. 2187 - 2190 (2006)
Enantioselective addition of ketones to aromatic aldehydes has been achieved with up to 88% enantiomeric excess, using the commercially available (S,S,S)-perhydroindolic acid catalyst.
Silica Jar-with-Lid as Chemo-Enzymatic Nano-Compartment for Enantioselective Synthesis inside Living Cells
Dubbu, Sateesh,Kim, Seonock,Kumar, Amit,Kumari, Nitee,Lee, In Su,Lim, Jongwon
supporting information, p. 16337 - 16342 (2021/06/28)
Nanodevices, harvesting the power of synthetic catalysts and enzymes to perform enantioselective synthesis inside cell, have never been reported. Here, we synthesized round bottom jar-like silica nanostructures (SiJARs) with a chemo-responsive metal-silic
Accelerating the optimization of enzyme-catalyzed synthesis conditionsviamachine learning and reactivity descriptors
Liang, Jinhu,Liu, Dongchang,Wan, Zhongyu,Wang, Quan-De
supporting information, p. 6267 - 6273 (2021/07/28)
Enzyme-catalyzed synthesis reactions are of crucial importance for a wide range of applications. An accurate and rapid selection of optimal synthesis conditions is crucial and challenging for both human knowledge and computer predictions. In this work, a
