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Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients: recent advances Full article

Journal Успехи химии
ISSN: 0042-1308
Output data Year: 2026, Volume: 95, Number: 8, Article number : RCR5237, Pages count : DOI: 10.59761/RCR5237
Authors Сухоруков А.Ю. 1 , Турова О.В. 1 , Злотин С.Г. 1
Affiliations
1 Институт органической химии им. Н.Д.Зелинского РАН, Москва, Российская Федерация

Abstract: Over the past decade, the chemistry of nitro compounds has been extensively developed. A particular focus of research has been placed on stereoselective transformations leading to key precursors of natural products and pharmaceutical ingredients. Most important among them are asymmetric reactions of nitroalkanes with electrophiles (e.g., Michael addition, Henry and nitro-Mannich reactions), nucleophilic additions and cycloadditions to nitroalkenes, cascade multistep processes, and novel strategies for the stereoselective introduction of the nitro group. Precise stereocontrol in these reactions is achieved through the application of new efficient organocatalysts, including solid-supported ones, as well as enzymatic and biocatalytic approaches that directly involve nitro compounds. Herein, we have systematized recently published data on the application of nitro compounds for the target-oriented stereoselective synthesis of natural and artificial bioactive molecules. The review covers the period from 2016 to 2026. The bibliography includes 283 references.
Cite: Сухоруков А.Ю. , Турова О.В. , Злотин С.Г.
Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients: recent advances
Успехи химии. 2026. Т.95. №8. RCR5237 . DOI: 10.59761/RCR5237
Translated: Sukhorukov A.Y. , Turova O.V. , Zlotin S.G.
Stereoselective reactions of nitro compounds in the synthesis of natural compound analogs and active pharmaceutical ingredients: recent advances
Russian Chemical Reviews. 2026. V.95. N8. RCR5237 . WOS OpenAlex
Dates:
Submitted: May 13, 2026
Published online: Aug 14, 2026
Identifiers: No identifiers
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