Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Igor V. Chistyakov"'
Autor:
Dmitry B. Eremin, Alexey S. Galushko, Daniil A. Boiko, Evgeniy O. Pentsak, Igor V. Chistyakov, Valentine P. Ananikov
Publikováno v:
Journal of the American Chemical Society. 144:6071-6079
Homogeneous catalysis is typically considered "well-defined" from the standpoint of catalyst structure unambiguity. In contrast, heterogeneous nanocatalysis often falls into the realm of "poorly defined" systems. Supported catalysts are difficult to
Autor:
Zoya A. Starikova, Valentine P. Ananikov, Levon L. Khemchyan, Igor V. Chistyakov, Nikolay V. Orlov, Irina P. Beletskaya
Publikováno v:
The Journal of Organic Chemistry. 79:12111-12121
A unique Ni-catalyzed transformation is reported for the one-pot highly selective synthesis of previously unknown monoseleno-substituted 1,3-dienes starting from easily available terminal alkynes and benzeneselenol. The combination of a readily avail
Autor:
Igor V. Chistyakov, Zoya A. Starikova, Irina P. Beletskaya, Valentine P. Ananikov, Nikolay V. Orlov
Publikováno v:
Russian Chemical Bulletin. 62:47-54
An efficient catalytic system based on easily available palladium acetate was developed for the selective addition of aliphatic thiols to the triple bond of internal alkynes. Formed in situ [M(SR)2]n nanostructured particles were found to be an activ
Autor:
Nikolay V. Orlov, Valentine P. Ananikov, Zoya A. Starikova, Levon L. Khemchyan, Irina P. Beletskaya, Igor V. Chistyakov
Publikováno v:
ChemInform. 46
A unique Ni-catalyzed transformation is reported for the one-pot highly selective synthesis of previously unknown monoseleno-substituted 1,3-dienes starting from easily available terminal alkynes and benzeneselenol. The combination of a readily avail
Autor:
Zoya A. Starikova, Irina P. Beletskaya, Nikolay V. Orlov, Igor V. Chistyakov, Valentine P. Ananikov
Publikováno v:
ChemInform. 45
An efficient catalytic system based on easily available palladium acetate was developed for the selective addition of aliphatic thiols to the triple bond of internal alkynes. Formed in situ [M(SR)2]n nanostructured particles were found to be an activ