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Mendeleev Communications, 2025, Volume 35, Issue 6, Pages 642–644
DOI: https://doi.org/10.71267/mencom.7796
(Mi mendc7326)
 

Communications

Chiral hydrogen-bonded frameworks featuring proline motifs as heterogeneous catalysts for the enantioselective synthesis of warfarin

I. S. Aniskina, M. A. Shandyboab, S. A. Kuznetsovaa, K. O. Biriukova, M. M. Ilyin Jr.a, M. G. Ezernitskayaa, S. P. Kutumova, A. S. Poghosyanc, A. S. Saghyanc, V. P. Chernyshevd, D. A. Chusova, Yu. N. Belokona

a A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 119334 Moscow, Russian Federation
b National Research University Higher School of Economics (HSE University), 101000 Moscow, Russian Federation
c Scientific and Production Center ‘Armbiotechnology’, National Academy of Sciences of Republic Armenia, 0056 Yerevan, Armenia
d JSC ‘Shchelkovo Agrokhim’, 141101 Shchelkovo, Moscow Region, Russian Federation
References:
Abstract: Chiral hydrogen-bonded organic frameworks incorporating proline motifs were synthesized from tetrakis-, bis- or monoprolinamide precursors and di- or tetracarboxylic or sulfonic acids. Their testing as heterogeneous catalysts for the synthesis of warfarin provided product yields of up to 84% with ee values of up to 45%.
Keywords: heterogeneous catalysis, hydrogen-bonded organic frameworks, asymmetric catalysis, chiral tetraamines, warfarin, proline.
Funding agency Grant number
The RA MES State Committee of Science SCS 21AG-1D013
Ministry of Science and Higher Education of the Russian Federation contract no. 075-00276-25-00
Received: 09.04.2025
Accepted: 17.06.2025
Published: 21.10.2025
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (2.2 Mb)


Citation: I. S. Aniskin, M. A. Shandybo, S. A. Kuznetsova, K. O. Biriukov, M. M. Ilyin Jr., M. G. Ezernitskaya, S. P. Kutumov, A. S. Poghosyan, A. S. Saghyan, V. P. Chernyshev, D. A. Chusov, Yu. N. Belokon, “Chiral hydrogen-bonded frameworks featuring proline motifs as heterogeneous catalysts for the enantioselective synthesis of warfarin”, Mendeleev Commun., 35:6 (2025), 642–644
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