Zobrazeno 1 - 10
of 12
pro vyhledávání: '"S. F. PAVLOV"'
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 24:579-581
The reaction of trimethyliodosilane with tetraalkoxysilanes, taken in a 1–3 ∶1 mole ratio, leads to a mixture of trimethylsiloxy derivatives [(CH3)3SiO]nSi(OR)4-n with n = 1–4. Tetrakis(trimethylsiloxy)silane (n = 4) is the main reaction produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3154449a9508364e851604c340734cdb
https://doi.org/10.1007/bf00927482
https://doi.org/10.1007/bf00927482
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ce9d8b2a8a90c995ea35b5e14fe24ac
https://doi.org/10.1002/chin.197651242
https://doi.org/10.1002/chin.197651242
Publikováno v:
Chemischer Informationsdienst. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee69b433360861e3a8c95b4e3142e153
https://doi.org/10.1002/chin.197632242
https://doi.org/10.1002/chin.197632242
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
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8a8ffd798882d3589fc70847b464506
https://doi.org/10.1002/chin.197514305
https://doi.org/10.1002/chin.197514305
Publikováno v:
Chemischer Informationsdienst. 8
alkyl aryl ethers react with trimethyliodosilane at 120–135° in the absence of a catalyst to give the corresponding trimethylaroxysilanes and alkyl halide. An increase in the length of the alkyl radical or the insertion of a substituent in the o-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd0f511af7b68cc27326fe50e045b7a9
https://doi.org/10.1002/chin.197711276
https://doi.org/10.1002/chin.197711276
Publikováno v:
Chemischer Informationsdienst. 6
The reaction of trimethyliodosilane with tetraalkoxysilanes, taken in a 1–3 ∶1 mole ratio, leads to a mixture of trimethylsiloxy derivatives [(CH3)3SiO]nSi(OR)4-n with n = 1–4. Tetrakis(trimethylsiloxy)silane (n = 4) is the main reaction produc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a52533a1bf9d0abe6f9cba5914df54ba
https://doi.org/10.1002/chin.197530285
https://doi.org/10.1002/chin.197530285
Autor:
S. F. Pavlov, M. G. Voronkov
Publikováno v:
Chemischer Informationsdienst. 4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e3b14c678a3c0d51655340c13ab6b96
https://doi.org/10.1002/chin.197339295
https://doi.org/10.1002/chin.197339295
Publikováno v:
Gigiena i sanitariia. 37(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc44e68adffeba35fa78d93ebed11f1f
https://pubmed.ncbi.nlm.nih.gov/5052194
https://pubmed.ncbi.nlm.nih.gov/5052194
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 25:2198-2199
alkyl aryl ethers react with trimethyliodosilane at 120–135° in the absence of a catalyst to give the corresponding trimethylaroxysilanes and alkyl halide. An increase in the length of the alkyl radical or the insertion of a substituent in the o-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6476314b38eec66117751f3ce2ded60
https://doi.org/10.1007/bf02659549
https://doi.org/10.1007/bf02659549