Asymmetric organocatalysis: from a breakthrough methodology to sustainable catalysts and processes Full article
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Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285 |
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| Output data | Year: 2023, Volume: 72, Number: 1, Pages: 42-60 Pages count : 19 DOI: 10.1007/s11172-023-3713-5 | ||
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Abstract:
The evolution of modern catalytic methodologies for asymmetric organic synthesis, including transition metal and organocatalysis, is briefly considered. The results of the authors’ research group comprise the development of convenient, efficient, and reusable metal-free amine-containing catalysts (aminocatalysts) for manufacturing enantiomerically enriched organic compounds. The efficiency of the obtained catalysts is demonstrated for asymmetric aldol reactions, Michael reactions, and domino reactions, including green chemistry processes. The applicability of the developed catalysts and processes for the synthesis of natural product analogs and the most active enantiomers of clinically used drugs is demonstrated.
Cite:
Kucherenko A.S.
, Zlotin S.G.
Asymmetric organocatalysis: from a breakthrough methodology to sustainable catalysts and processes
Russian Chemical Bulletin. 2023. V.72. N1. P.42-60. DOI: 10.1007/s11172-023-3713-5 WOS Scopus OpenAlex
Asymmetric organocatalysis: from a breakthrough methodology to sustainable catalysts and processes
Russian Chemical Bulletin. 2023. V.72. N1. P.42-60. DOI: 10.1007/s11172-023-3713-5 WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:000933481700003 |
| Scopus: | 2-s2.0-85148444615 |
| OpenAlex: | W4320736149 |