Entity

Time filter

Source Type

Moscow, Russia

Panchenko S.P.,Moscow Chemical Lyceum | Runichina S.A.,Moscow Chemical Lyceum | Tumanov V.V.,RAS N. D. Zelinsky Institute of Organic Chemistry
Mendeleev Communications | Year: 2011

Hydrogen bond donating capacity of hexafluoroisopropanol was shown to be responsible for both the formation of its stoichiometric complexes with aldehydes and acetals and subsequent facilitation of their reactions with allylsilanes. © 2011 Mendeleev Communications. All rights reserved. Source


Shalamova E.A.,Moscow Chemical Lyceum | Lee Y.,Korea Advanced Institute of Science and Technology | Chung G.,Korea Advanced Institute of Science and Technology | Semakin A.N.,RAS N. D. Zelinsky Institute of Organic Chemistry | And 5 more authors.
Tetrahedron Letters | Year: 2014

A general strategy for the assembly of previously unknown tris(β,β,γ-oximinoalkyl)amines from aliphatic nitro compounds and methyl vinyl ketone is described. The strategy involves N,N-bis(siloxy) enamines as key intermediates. The latter are accessible by double silylation of alkylnitro compounds. Nickel(II) and copper(II) complexes of tris(β,β,γ-oximinoalkyl)amines are prepared and structurally characterized. © 2014 Elsevier Ltd. All rights reserved. Source


Levin V.V.,RAS N. D. Zelinsky Institute of Organic Chemistry | Trifonov A.L.,Moscow Chemical Lyceum | Zemtsov A.A.,RAS N. D. Zelinsky Institute of Organic Chemistry | Struchkova M.I.,RAS N. D. Zelinsky Institute of Organic Chemistry | And 2 more authors.
Organic Letters | Year: 2014

A method for nucleophilic difluoromethylation of reactive Michael acceptors, aldehydes, and azomethines is described. The reaction is performed using the readily available and air-stable reagent difluoromethylene phosphabetaine. The process involves interaction of an electrophilic substrate with in situ generated difluorinated phosphonium ylide followed by hydrolysis of the carbon-phosphorus bond under mild conditions. © 2014 American Chemical Society. Source


Naumovich Y.A.,RAS N. D. Zelinsky Institute of Organic Chemistry | Buckland V.E.,National Junior College | Sen'ko D.A.,Moscow Chemical Lyceum | Nelyubina Y.V.,RAS Nesmeyanov Institute of Organoelement Compounds | And 3 more authors.
Organic and Biomolecular Chemistry | Year: 2016

The synthesis of α-nitroxy-substituted oxime derivatives has been achieved by an unprecedented metal-assisted addition of a nitrate anion to bis(oxy)enamines, which are readily available from nitronates or nitroalkanes. The method has a broad scope and provides access to α-nitroxy-oximes and their cyclic ethers including nitroxy-substituted isoxazolines and dihydro-1,2-oxazines, which are of interest as potential NO-donors and intermediates in the synthesis of bioactive molecules. © The Royal Society of Chemistry 2016. Source


Lvov A.G.,RAS N. D. Zelinsky Institute of Organic Chemistry | Milevsky N.A.,Moscow Chemical Lyceum | Shirinian V.Z.,RAS N. D. Zelinsky Institute of Organic Chemistry | Krayushkin M.M.,RAS N. D. Zelinsky Institute of Organic Chemistry
Chemistry of Heterocyclic Compounds | Year: 2015

A two-stage preparative method is proposed for the synthesis of dithienylacetylenes - widely used intermediates in the preparation of photochromic diarylethenes. © 2015 Springer Science+Business Media New York. Source

Discover hidden collaborations