Zobrazeno 1 - 9
of 9
pro vyhledávání: '"N. N. Preobrazhenskaya"'
Autor:
N. N. Preobrazhenskaya
Publikováno v:
Plant Indicators of Soils, Rocks, and Subsurface Waters ISBN: 9781489949165
Plant Indicators of Soils, Rocks, and Subsurface Waters
Plant Indicators of Soils, Rocks, and Subsurface Waters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38b0f0fb4476fc3eca3eddfc4b8d1b25
https://doi.org/10.1007/978-1-4899-4914-1_19
https://doi.org/10.1007/978-1-4899-4914-1_19
Autor:
N. N. Preobrazhenskaya
Publikováno v:
Plant Indicators of Soils, Rocks, and Subsurface Waters ISBN: 9781489949165
Plant Indicators of Soils, Rocks, and Subsurface Waters
Plant Indicators of Soils, Rocks, and Subsurface Waters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::356e9d1dc6899701ac7505ab7c6ddaf7
https://doi.org/10.1007/978-1-4899-4914-1_40
https://doi.org/10.1007/978-1-4899-4914-1_40
Publikováno v:
Plant Indicators of Soils, Rocks, and Subsurface Waters ISBN: 9781489949165
Plant Indicators of Soils, Rocks, and Subsurface Waters
Plant Indicators of Soils, Rocks, and Subsurface Waters
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cce5a1c635c9fba95cfdbb960cecac9c
https://doi.org/10.1007/978-1-4899-4914-1_39
https://doi.org/10.1007/978-1-4899-4914-1_39
Publikováno v:
Chemistry of Natural Compounds. 3:101-104
The hydrolysis of nucleotidyl (5′ → N) phenylalanines with free carboxy groups has been studied. It has been found that in an acid medium the cleavage of the phosphate bond takes place simultaneously with that of the phosphoramide bond. The intro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::059d2bec927a112e991c6156be272fce
https://doi.org/10.1007/bf00567178
https://doi.org/10.1007/bf00567178
Autor:
N N Preobrazhenskaya
Publikováno v:
Russian Chemical Reviews. 41:54-65
The mechanisms of the hydrolysis and solvolysis of phosphoramidic acids have been examined. The concepts of phosphoramidates as donors of the phosphate residue in phosphorylation reactions of acids, alcohols, and amines are discussed. The use of phos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fb4650efe1b3c0ad333e93e1db039c0
https://doi.org/10.1070/rc1972v041n01abeh002030
https://doi.org/10.1070/rc1972v041n01abeh002030
Autor:
N N Preobrazhenskaya, Zoya A Shabarova
Publikováno v:
Russian Chemical Reviews. 38:111-125
This review deals with the literature data on the conformations and intramolecular interactions of nucleosides, nucleotides, and their derivatives: nucleotide esters, nucleoside cyclic phosphates, oligonucleotides, nucleoside pyrophosphates (includin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d5e4a0d1c45fa6cd28526fbd3a07b17
https://doi.org/10.1070/rc1969v038n02abeh001730
https://doi.org/10.1070/rc1969v038n02abeh001730
Publikováno v:
Chemistry of Natural Compounds. 1:269-272
1. The methyl ester of polyuridylyl-(5′→N)-phenylalanine containing an average of 13 nucleotide residues has been synthesized by the carbodiimide method.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45f55939cde707cac9ad160e3ecf41f3
https://doi.org/10.1007/bf00563701
https://doi.org/10.1007/bf00563701
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 18:2157-2159
1. Derivatives of uridylyl-(5′ → N)-phenylalanine were obtained, methylated on the ring nitrogen N3 and the phosphoric acid radical. 2. In studies of acid, alkaline, and enzyme hydrolysis of these compounds, it was established that CH3-groups in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6e30a8e849725cb6cdb36ef374bec38
https://doi.org/10.1007/bf00906642
https://doi.org/10.1007/bf00906642
Publikováno v:
Molecular biology. 5(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2202f92f3e26c8abbb79ecfd019c697e
https://pubmed.ncbi.nlm.nih.gov/5154816
https://pubmed.ncbi.nlm.nih.gov/5154816