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pro vyhledávání: '"Yu. I. Nein"'
Autor:
Yu. Yu. Morzherin, Yu. I. Nein
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:1021-1026
4-Carbamoyl-3-cyanomethyl-1,2,3-triazolium-5-olates were shown to cyclize when treated with sodium ethoxide giving zwitterionic 6-amino-4-oxo-4,5-dihydro-2Н-1,2,3-triazolo[1,5-а]pyrazinium-3-olates. In contrast to 4-carbamoyl-3-cyanomethyl-1,2,3-tr
Autor:
Yu. I. Nein, P. E. Kropotina, M. F. Kosterina, Tatiana V. Glukhareva, E. V. Deeva, Yu. Yu. Morzherin
Publikováno v:
Chemistry of Heterocyclic Compounds. 43:76-81
The synthesis of 2,3,4,4a,5,6-hexahydro-6H-spiro[benzo[c]quinolizine-5,4′-pyrazol]-5′-ones has been achieved by the reaction of 2-piperidinobenzaldehydes with 2-aryl-5-methyl-2,4-dihydropyrazol-3-one via the “tert-amino effect” mechanism.
Publikováno v:
Chemistry of Heterocyclic Compounds. 42:1472-1477
Condensed mesoionic 1,2,3-triazoles containing an aryl or hetaryl substituent at N(2) in the ring have been synthesized by intramolecular condensation.
Autor:
Yu. Yu. Morzherin, Yu. I. Nein
Publikováno v:
Russian Chemical Bulletin
The quantum chemical calculations of the basic criteria for aromaticity (nucleus-independent chemical shift (NICS), aromatic stabilization energy (ASE), and parameters of harmonic oscillator model of aromaticity (HOMA), and geometric indices (I 5)) o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf39e075cdbc3b4d179526fb047884ca
https://hdl.handle.net/10995/51461
https://hdl.handle.net/10995/51461
Autor:
Tatiana V. Glukhareva, E. V. Deeva, Yu. I. Nein, M. F. Kosterina, P. E. Kropotina, Yu. Yu. Morzherin
Publikováno v:
ChemInform. 38
The synthesis of 2,3,4,4a,5,6-hexahydro-6H-spiro[benzo[c]quinolizine-5,4′-pyrazol]-5′-ones has been achieved by the reaction of 2-piperidinobenzaldehydes with 2-aryl-5-methyl-2,4-dihydropyrazol-3-one via the “tert-amino effect” mechanism.
Publikováno v:
ChemInform. 36
A selective procedure was developed for the synthesis of 1,2,3-triazoles and unsymmetrically substituted diazomalonamides. Cyclization of unsymmetrically substituted diazomalonamides to 1,2,3-triazoles was studied by the method of intramolecular comp
Publikováno v:
ChemInform. 34
Publikováno v:
Chemistry of Heterocyclic Compounds. 42:412-413
Publikováno v:
Chemistry of Heterocyclic Compounds. 41:940-941
Publikováno v:
Russian Chemical Bulletin; Jun2004, Vol. 53 Issue 6, p1305-1310, 6p