Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Evgeniya Podyacheva"'
Autor:
Artemy R. Fatkulin, Vasily Korochantsev, Oleg I. Afanasyev, Evgeniya Podyacheva, Olga Chusova, Dmitry V. Muratov, Maria I. Godovikova, Sergei Semenov, Denis Chusov
Publikováno v:
New Journal of Chemistry. 47:6532-6535
Herein we report a transition-metal- and acid-free protocol for the reductive amination of carbonyl compounds with DMF using a substoichiometric amount of NaH2PO2·H2O. The general trends and limitations of the method were explored.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2224426d8cb3cabcf9779f54f0719def
https://doi.org/10.1039/d3nj00728f
https://doi.org/10.1039/d3nj00728f
Publikováno v:
ACS Catalysis. 12:5145-5154
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51449420252f526e3f20c7e85e1ecd81
https://doi.org/10.1021/acscatal.2c01000
https://doi.org/10.1021/acscatal.2c01000
Autor:
Evgeniya Podyacheva, Alexandra I. Balalaeva, Oleg I. Afanasyev, Sofiya A. Runikhina, Olga Chusova, Andrey S. Kozlov, Saihu Liao, Denis Chusov
Publikováno v:
New Journal of Chemistry.
Syngas (a mixture of H2 and CO) is a synergistic reducing agent working much better than its components independently. In particular it allows to aminate carbonyl compounds with unstable functional groups furnishing the potential fungicides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13b3b430865d517cdefdaaed4a34e68b
https://doi.org/10.1039/d3nj01258a
https://doi.org/10.1039/d3nj01258a
Autor:
Maria Makarova, Oleg I. Afanasyev, Alexander Rudenko, Evgeniya Podyacheva, Alexey A. Tsygankov, Denis Chusov
Publikováno v:
The Journal of Organic Chemistry. 85:9347-9360
A total synthesis of the vasicinone family of natural products from bulk chemicals was developed. Reductive condensation of o-nitrobenzaldehydes with amines utilizing iron pentacarbonyl as a reducing agent followed by subsequent oxidation leads to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1fc1e9c09b0f8109e85bd04ac64b805
https://doi.org/10.1021/acs.joc.0c00794
https://doi.org/10.1021/acs.joc.0c00794
Publikováno v:
ACS catalysis 12(12), 7142-7198 (2022). doi:10.1021/acscatal.2c01133
Borrowing hydrogen or the hydrogen autotransfer amination is a powerful approach to create single C-N bonds starting from stable and readily available substrates: amines and alcohols. It is considered as one of the most atom-efficient and green metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6f0b856007ddd13fbd62817cd9d08f5
https://hdl.handle.net/2128/33947
https://hdl.handle.net/2128/33947
Autor:
Dmitry V. Muratov, Yulia V. Nelyubina, Gleb L. Denisov, Vladimir B. Kharitonov, Alexander S. Peregudov, Denis Chusov, Evgeniya Podyacheva, Dmitry A. Loginov
Publikováno v:
Organometallics. 38:3151-3158
The η6-fluorene cyclopentadienyl complexes [(η5-C5R5)M(η6-fluorene)](SbF6)2 (1: M = Co, R = Me; 2a: M = Rh, R = H; 2b: M = Ir, R = H) were synthesized by the iodide abstraction from [(η5-C5R5)MI2]n...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f2cfea7c0e6094fd61a4df7101122ca
https://doi.org/10.1021/acs.organomet.9b00378
https://doi.org/10.1021/acs.organomet.9b00378
Publikováno v:
Synthesis. 51:2667-2677
A comparative study of various widely used methods of reductive amination is reported. Specifically, such reducing agents as H2, Pd/C, hydride reagents [NaBH4, NaBH3CN, NaBH(OAc)3], and CO/Rh2(OAc)4 system were considered. For understanding the selec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a837ac690cc07377dbacd5256ba3a3ae
https://doi.org/10.1055/s-0037-1611788
https://doi.org/10.1055/s-0037-1611788
Publikováno v:
Tetrahedron Letters. 60:575-582
The digest is devoted to the most widespread reducing agents which are used for the reduction of tertiary and secondary phosphine oxides, phospholene oxides, phospholane oxides, phosphonates, phosphinates, α- and β-hydroxy and thiomethyl phosphine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a822e33047b8f8eefe2a7d7d4e15da0
https://doi.org/10.1016/j.tetlet.2018.12.070
https://doi.org/10.1016/j.tetlet.2018.12.070
Autor:
Oleg I, Afanasyev, Evgeniya, Podyacheva, Alexander, Rudenko, Alexey A, Tsygankov, Maria, Makarova, Denis, Chusov
Publikováno v:
The Journal of organic chemistry. 85(14)
A total synthesis of the vasicinone family of natural products from bulk chemicals was developed. Reductive condensation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::572d038e6fa5b82f9c3a4ff5528e6531
https://pubmed.ncbi.nlm.nih.gov/32515592
https://pubmed.ncbi.nlm.nih.gov/32515592
Autor:
A. V. Medved’ko, V. N. Nuriev, Evgeniya Podyacheva, Anna A. Moiseeva, O. V. Fedorov, Artem I. Vedernikov, Sergey P. Gromov, N. A. Kurchavov, Sergey Z. Vatsadze, A. Ya. Freidzon
Publikováno v:
Russian Journal of Organic Chemistry. 53:1726-1737
The reaction of tetraethyl [1,3-phenylenedi(methylene)]bis(phosphonate) with formyl derivatives of benzocrown-ethers or formyl derivatives of o-dimethoxybenzene lead to high yield formation of the respectful bis(crown ether) containing 1,3-distyrylbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b08d9c7ab4b8278ddfd95f5ae8630f1
https://doi.org/10.1134/s1070428017110203
https://doi.org/10.1134/s1070428017110203