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Preparation of 3,5-diarylsubstituted 5-hydroxy-1,5-dihydro-2H -pyrrol-2-ones via base-assisted cyclization of 3-cyanoketones . Nicolai A. Aksenov, Dmitrii A. Aksenov, Igor A. Kurenkov, Alexander V. Aksenov, Anton A. Skomorokhov, Lidiya A. Prityko, Michael Rubin
, RSC Adv.
, 2021
, 11
, 16236
The second example of doubly enantiophobic behavior during crystallization: a detailed crystallographic, thermochemical and spectroscopic study . Daria P. Gerasimova, Alina F. Saifina, Dmitry V. Zakharychev, Robert R. Fayzullin, Almira R. Kurbangalieva, Olga A. Lodochnikova
, CrystEngComm
, 2021
, 23
, 3907
“Doubly enantiophobic” behavior during crystallization of racemic 1,5-dihydro-2H -pyrrol-2-one thioether . Olga A. Lodochnikova, Aigul R. Zaripova, Robert R. Fayzullin, Aida I. Samigullina, Irina I. Vandyukova, Lubov N. Potapova, Almira R. Kurbangalieva
, CrystEngComm
, 2018
, 20
, 3218
Cyclization of 5-(2-chloroethoxy)-1,5-dihydro-2H -pyrrol-2-ones . Kirill V. Nikitin, Nonna P. Andryukhova, Eung K. Ryu
, Mendeleev Commun.
, 2001
, 11
, 82
Reactions of pyrrole, imidazole, and pyrazole with ozone: kinetics and mechanisms . Agnes Tekle-Röttering, Sungeun Lim, Erika Reisz, Holger V. Lutze, Mohammad Sajjad Abdighahroudi, Sarah Willach, Winfried Schmidt, Peter R. Tentscher, Daniel Rentsch, Christa S. McArdell, Torsten C. Schmidt, Urs von Gunten
, Environ. Sci.: Water Res. Technol.
, 2020
, 6
, 976
5-Hydroxy-pyrrolone based building blocks as maleimide alternatives for protein bioconjugation and single-site multi-functionalization . Ewout De Geyter, Eirini Antonatou, Dimitris Kalaitzakis, Sabina Smolen, Abhishek Iyer, Laure Tack, Emiel Ongenae, Georgios Vassilikogiannakis, Annemieke Madder
, Chem. Sci.
, 2021
, 12
, 5246
Part I: Nitroalkenes in the synthesis of heterocyclic compounds . Azim Ziyaei Halimehjani, Irishi N. N. Namboothiri, Seyyed Emad Hooshmand
, RSC Adv.
, 2014
, 4
, 48022