دورية أكاديمية

Hypersensitive Inhibition of Organocatalysts by Halide Salts: Are Two Catalysts Involved in the Mannich Reaction?

التفاصيل البيبلوغرافية
العنوان: Hypersensitive Inhibition of Organocatalysts by Halide Salts: Are Two Catalysts Involved in the Mannich Reaction?
المؤلفون: Leino, Teppo O., Noutsias, Dimitris, Helttunen, Kaisa, Moilanen, Jani O., Tarkkonen, Eeki, Kalenius, Elina, Kiesilä, Anniina, Pihko, Petri M.
المصدر: European Journal of Organic Chemistry ; ISSN 1434-193X 1099-0690
بيانات النشر: Wiley
سنة النشر: 2024
المجموعة: Wiley Online Library (Open Access Articles via Crossref)
الوصف: Conformationally flexible tertiary amine – thiourea−urea catalysts 1 and 2 for the Mannich reaction between imines and malonate esters are efficiently inhibited by quaternary ammonium halides. NMR titrations, isothermal titration calorimetry (ITC) and NOE experiments showed that the catalysts bind chloride and bromide ions with relatively high affinities ( K =10 3 –10 5 M −1 in acetonitrile). The halide ions not only block the active site of the catalysts, but they also induce refolding into catalytically inactive conformations upon complexation in an allosteric‐like event. At substoichiometric inhibitor:catalyst ratios, the catalysts displayed hypersensitivity to the inhibitors, with overall rates that were lower than those expected from simple 1 st order kinetics and 1 : 1 inhibitor:catalyst stoichiometry. To rationalize the observed hypersensitivity, different kinetic scenarios were examined. For catalyst 2 and the Takemoto catalyst ( 6 ), the data is consistent with 2 nd order dependency on catalyst concentration, suggesting that a mechanism involving only a single catalyst in the catalytic cycle is not operative. For catalyst 1 , an alternative scenario involving 1 st order in catalyst and catalyst poisoning at low concentrations of 1 could also rationalize the hypersensitivity. Interestingly, inhibition of catalysts 1 and 2 by halide salts led to significant loss of enantioselectivity, in contrast to the Takemoto catalyst 6 which was inhibited but with essentially no change in enantioselectivity.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1002/ejoc.202400321
الإتاحة: https://doi.org/10.1002/ejoc.202400321Test
حقوق: http://creativecommons.org/licenses/by/4.0Test/
رقم الانضمام: edsbas.2B02C255
قاعدة البيانات: BASE