Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ken-ichiro Okuyama"'
Publikováno v:
New Journal of Chemistry. 24:221-228
A series of syn- and anti-[2.n]metacyclophan-1-enes, 3, and [2.n]metacyclophane-1,2-diols, 4, were prepared in good yields by a McMurry cyclization of 1,n-bis(5-tert-butyl-3-formyl-2-methoxyphenyl)alkanes, 2. Upon increasing the length of the methyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81910074cb6cb0e5634a88039f9a4288
https://doi.org/10.1039/b001145m
https://doi.org/10.1039/b001145m
Publikováno v:
Journal of Chemical Research. 2003:63-65
McMurry cyclisation of 1,2-bis(5- t-butyl-2-methyl-3-formylphenyl)ethane 2 afforded anti-[2.2]metacyclophan-1-ene 3 and anti-[2.2]metacyclophane-1,2-diols 4, which were converted into the corresponding 1,2-dione 6 by Swern oxidation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e74e0544a3bd6ac77c8e927ce35d0f2
https://doi.org/10.3184/030823403103173183
https://doi.org/10.3184/030823403103173183
Publikováno v:
ChemInform. 31
A series of syn- and anti-[2.n]metacyclophan-1-enes, 3, and [2.n]metacyclophane-1,2-diols, 4, were prepared in good yields by a McMurry cyclization of 1,n-bis(5-tert-butyl-3-formyl-2-methoxyphenyl)alkanes, 2. Upon increasing the length of the methyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a0126db60479c111fd5decd2c7b1e8a
https://doi.org/10.1002/chin.200029087
https://doi.org/10.1002/chin.200029087