Smol'yakov AF - Search Results

1

A synthetic route to artificial chiral α-amino acids featuring a 3,4-dihydroisoquinolone core through a Rh(III)-catalyzed functionalization of allyl groups in chiral Ni(II) complexes.

Arsenov MA, Stoletova NV, Smol'yakov AF, Savel'yeva TF, Maleev VI, Loginov DA, Larionov VA. Arsenov MA, et al. Among authors: smol yakov af. Org Biomol Chem. 2023 Nov 29;21(46):9143-9149. doi: 10.1039/d3ob01513k. Org Biomol Chem. 2023. PMID: 37982196

2

Remarkable Structural and Electronic Features of the Complex Formed by Trimeric Copper Pyrazolate with Pentaphosphaferrocene.

Filippov OA, Titov AA, Guseva EA, Loginov DA, Smol'yakov AF, Dolgushin FM, Belkova NV, Epstein LM, Shubina ES. Filippov OA, et al. Chemistry. 2015 Sep 14;21(38):13176-80. doi: 10.1002/chem.201502085. Chemistry. 2015. PMID: 26332228

3

Reductive amination catalyzed by iridium complexes using carbon monoxide as a reducing agent.

Moskovets AP, Usanov DL, Afanasyev OI, Fastovskiy VA, Molotkov AP, Muratov KM, Denisov GL, Zlotskii SS, Smol'yakov AF, Loginov DA, Chusov D. Moskovets AP, et al. Org Biomol Chem. 2017 Aug 2;15(30):6384-6387. doi: 10.1039/c7ob01005b. Org Biomol Chem. 2017. PMID: 28726957

4

Interaction of a trinuclear copper(i) pyrazolate with alkynes and carbon-carbon triple bond activation.

Titov AA , Larionov VA , Smol'yakov AF , Godovikova MI , Titova EM , Maleev VI , Shubina ES . Titov AA , et al. Chem Commun (Camb). 2019 Jan 2;55(3):290-293. doi: 10.1039/c8cc08592g. Chem Commun (Camb). 2019. PMID: 30411109

5

Henry Reaction Revisited. Crucial Role of Water in an Asymmetric Henry Reaction Catalyzed by Chiral NNO-Type Copper(II) Complexes.

Larionov VA, Yashkina LV, Medvedev MG, Smol'yakov AF, Peregudov AS, Pavlov AA, Eremin DB, Savel'yeva TF, Maleev VI, Belokon YN. Larionov VA, et al. Inorg Chem. 2019 Aug 19;58(16):11051-11065. doi: 10.1021/acs.inorgchem.9b01574. Epub 2019 Aug 1. Inorg Chem. 2019. PMID: 31369247

6

Effect of Cp-Ligand Methylation on Rhodium(III)-Catalyzed Annulations of Aromatic Carboxylic Acids with Alkynes: Synthesis of Isocoumarins and PAHs for Organic Light-Emitting Devices.

Molotkov AP, Arsenov MA, Kapustin DA, Muratov DV, Shepel' NE, Fedorov YV, Smol'yakov AF, Knyazeva EI, Lypenko DA, Dmitriev AV, Aleksandrov AE, Maltsev EI, Loginov DA. Molotkov AP, et al. Chempluschem. 2020 Feb;85(2):334-345. doi: 10.1002/cplu.202000048. Chempluschem. 2020. PMID: 32048812

7

The charge-assisted hydrogen-bonded organic framework (CAHOF) self-assembled from the conjugated acid of tetrakis(4-aminophenyl)methane and 2,6-naphthalenedisulfonate as a new class of recyclable Brønsted acid catalysts.

Kuznetsova SA, Gak AS, Nelyubina YV, Larionov VA, Li H, North M, Zhereb VP, Smol'yakov AF, Dmitrienko AO, Medvedev MG, Gerasimov IS, Saghyan AS, Belokon YN. Kuznetsova SA, et al. Beilstein J Org Chem. 2020 May 26;16:1124-1134. doi: 10.3762/bjoc.16.99. eCollection 2020. Beilstein J Org Chem. 2020. PMID: 32550927 Free PMC article.

8

A general asymmetric synthesis of artificial aliphatic and perfluoroalkylated α-amino acids by Luche's cross-electrophile coupling reaction.

Gugkaeva ZT, Smol'yakov AF, Maleev VI, Larionov VA. Gugkaeva ZT, et al. Org Biomol Chem. 2021 Jun 28;19(24):5327-5332. doi: 10.1039/d1ob00805f. Epub 2021 May 27. Org Biomol Chem. 2021. PMID: 34042928

9

Synthesis and a Catalytic Study of Diastereomeric Cationic Chiral-at-Cobalt Complexes Based on (R,R)-1,2-Diphenylethylenediamine.

Emelyanov MA, Stoletova NV, Smol'yakov AF, Il'in MM, Maleev VI, Larionov VA. Emelyanov MA, et al. Inorg Chem. 2021 Sep 20;60(18):13960-13967. doi: 10.1021/acs.inorgchem.1c00855. Epub 2021 Aug 27. Inorg Chem. 2021. PMID: 34449202

10

Family of Well-Defined Chiral-at-Cobalt(III) Complexes as Metal-Templated Hydrogen-Bond-Donor Catalysts: Effect of Chirality at the Metal Center on the Stereochemical Outcome of the Reaction.

Khromova OV, Emelyanov MA, Smol'yakov AF, Fedyanin IV, Maleev VI, Larionov VA. Khromova OV, et al. Inorg Chem. 2022 Apr 11;61(14):5512-5523. doi: 10.1021/acs.inorgchem.1c03927. Epub 2022 Mar 31. Inorg Chem. 2022. PMID: 35357165

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