Zobrazeno 1 - 7
of 7
pro vyhledávání: '"V. E. Puzanova"'
Autor:
V. E. Puzanova, Z. N. Parnes, D. N. Kursanov, M. M. Gol'din, G. D. Kolomnikova, M. I. Kalinkin
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 26:1713-1717
1. Acetylcymantrene, acetylferrocene, and acetylbenchrotrene form stable anionic σ complexes with trinitrobenzene. 2. Trinitrophenylacetylcymantrene, trinitrophenylacetylferrocene, and trinitrophenyl-acetylbenchrotrene have been synthesized by the o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d0e448d9cd2e7edd5cd3953303356ae
https://doi.org/10.1007/bf00925183
https://doi.org/10.1007/bf00925183
Autor:
A. D. Khmelinskaya, D. N. Kursanov, V. E. Puzanova, Z. N. Parnes, S. M. Shein, M. I. Kalinkin
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6802113a42b159801e63d63b23750588
https://doi.org/10.1002/chin.197408152
https://doi.org/10.1002/chin.197408152
Publikováno v:
Chemischer Informationsdienst. 6
The reaction of tetrahydrofuran with trimethyliodosilane under mild conditions gives trimethyl-(4-iodobutoxy)silane in quantitative yield. 1-Trimethylsilyl-4-trimethylsiloxybutane (10% yield) and the previously unknown 1,8-bis(trimethylsiloxy)octane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc043f8892ee9855b1c6e56e4838e1cb
https://doi.org/10.1002/chin.197526312
https://doi.org/10.1002/chin.197526312
Autor:
M. I. Kalinkin, Z. N. Parnes, M. M. Gol'din, V. E. Puzanova, G. D. Kolomnikova, D. N. Kursanova
Publikováno v:
Chemischer Informationsdienst. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cbfefc5d334d9176709292ef8c124e9
https://doi.org/10.1002/chin.197805292
https://doi.org/10.1002/chin.197805292
Autor:
L. A. Borisova, Z. N. Parnes, V. E. Puzanova, D. N. Kursanov, G. D. Kolomnikova, M. I. Kalinkin
Publikováno v:
Chemischer Informationsdienst. 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0a7471167d6515302432c3a0ebb147d
https://doi.org/10.1002/chin.197242417
https://doi.org/10.1002/chin.197242417
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 24:377-378
The reaction of tetrahydrofuran with trimethyliodosilane under mild conditions gives trimethyl-(4-iodobutoxy)silane in quantitative yield. 1-Trimethylsilyl-4-trimethylsiloxybutane (10% yield) and the previously unknown 1,8-bis(trimethylsiloxy)octane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d198d4800741175714bf7655b31dc4b
https://doi.org/10.1007/bf00925793
https://doi.org/10.1007/bf00925793
Autor:
M. I. Kalinkin, L. A. Borisova, G. D. Kolomnikova, V. E. Puzanova, Z. N. Parnes, D. N. Kursanov
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 21:1412-1412
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1e21b7a327b591ee24f1d5e6b6dc0fe
https://doi.org/10.1007/bf00854588
https://doi.org/10.1007/bf00854588