Three-step alkylaminomethylative α, β-difunctionalization of enones
EM Buev, VS Moshkin, VY Sosnovskikh - Organic Chemistry Frontiers, 2025 - pubs.rsc.org
Aminomethylation of alkenes is a convenient methodology for the synthesis of aliphatic
amines. This direction encompasses various methods, mainly allowing functionalization of …
amines. This direction encompasses various methods, mainly allowing functionalization of …
Straightforward synthesis of 3-substituted pyrrolidines from active methylene compounds, sarcosine and formaldehyde
EV Gorbunova, VS Moshkin, VD Fedorenko… - Tetrahedron …, 2022 - Elsevier
Straightforward synthesis of 3-substituted pyrrolidines from active methylene compounds,
sarcosine and formaldehyde - ScienceDirect Skip to main contentSkip to article Elsevier logo …
sarcosine and formaldehyde - ScienceDirect Skip to main contentSkip to article Elsevier logo …
Synthesis of Spiro[pyrrole-3,2'-pyrrolo[2,1-b]oxazoles] via 1,3-Dipolar Cycloaddition of 1H-Pyrrole-2,3-diones to Azomethine Ylides
AA Moroz, MV Dmitriev, AN Maslivets - Russian Journal of Organic …, 2023 - Springer
Abstract The 1, 3-dipolar cycloaddition of 1 H-pyrrole-2, 3-diones to azomethine ylides
generated in situ by the condensation of L-proline and arylcarbaldehydes proceeds regio …
generated in situ by the condensation of L-proline and arylcarbaldehydes proceeds regio …
Phosphonium ylides in the multicomponent synthesis of pyrrolidines
EM Buev, PA Khardina, VS Moshkin, VY Sosnovskikh - Tetrahedron Letters, 2022 - Elsevier
A multicomponent synthesis of pyrrolidines starting from phosphonium ylides, N-
alkylglycines and carbonyl compounds was performed in 37–87% yields. This approach is …
alkylglycines and carbonyl compounds was performed in 37–87% yields. This approach is …
Catalyst‐/Additive‐Free One‐Pot Synthesis of Oxazolidines in Water via Regioselective and Stereoselective C− H Functionalization Approach
I Rahman, B Baruah, BK Rajbongshi, ML Deb… - …, 2023 - Wiley Online Library
A catalyst‐free approach for the synthesis of oxazolidine derivatives is developed here.
Though the synthesized oxazolidines contain three stereogenic centers, single diastereomer …
Though the synthesized oxazolidines contain three stereogenic centers, single diastereomer …
Reactions of Aldehydes and Ketones and Their Derivatives
MG Moloney - Organic Reaction Mechanisms 2020, 2024 - Wiley Online Library
The gold‐catalyzed cyclization of 2‐alkynylarylaldehyde cyclic acetals leads to indanone
derivatives in good‐to‐excellent yields. It is possible to use photoimmobilized Ni clusters on …
derivatives in good‐to‐excellent yields. It is possible to use photoimmobilized Ni clusters on …
Reaction of N-benzyl azomethine ylide with aryl isothiocyanates: synthesis of (Z)-N-aryl-3-benzylthiazolidine-5-imines
EM Buev, AP Osintseva, VS Moshkin… - Chemistry of …, 2020 - Springer
The reaction of aryl isothiocyanates with nonstabilized azomethine ylides generated in situ
by various methods was studied. It was established that the use of N-(methoxymethyl)-N …
by various methods was studied. It was established that the use of N-(methoxymethyl)-N …
Учредители: Российская академия наук
ЛВ Клыба, НА Недоля, ЕР Санжеева… - ЖУРНАЛ …, 2021 - elibrary.ru
Впервые изучена фрагментация 5-[(цианометил-и 1, 3-диоксолан-2-илметил)
сульфанил]-1 H-пиррол-2аминов в условиях электронной (70 эВ) и химической (газ …
сульфанил]-1 H-пиррол-2аминов в условиях электронной (70 эВ) и химической (газ …
[PDF][PDF] Synthèse de Mimes de Peptides à Motif Oxazolidine et Oxazolidinone.
I LAZOUNI - 2022 - dspace1.univ-tlemcen.dz
Le travail de cette thèse montre l'intérêt que portent les mimes de peptides et plus
particulièrement leur utilisation dans le domaine pharmaceutique. Ce domaine trouve une …
particulièrement leur utilisation dans le domaine pharmaceutique. Ce domaine trouve une …
Straightforward Synthesis of 3-Substituted Pyrrolidines from Active Methylene Compounds, Sarcosine and Formaldehyde
V Moshkin, EV Gorbunova, VD Fedorenko… - Sarcosine and … - papers.ssrn.com
Graphical Abstract Page 1 * Corresponding author. Tel: +7 3432616824; fax: +7
3432615978. E-mail address: evgenybuev@yandex.ru (EM Buev). Graphical Abstract …
3432615978. E-mail address: evgenybuev@yandex.ru (EM Buev). Graphical Abstract …