Zobrazeno 1 - 10
of 10
pro vyhledávání: '"C. F. Marth"'
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1503d1ed3fa8347f5dd2d17f951302f
https://doi.org/10.1002/chin.199243084
https://doi.org/10.1002/chin.199243084
Autor:
E. Vedejs, C. F. Marth
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7185cbd76e532d4c2f9c6cb7821d6fe1
https://doi.org/10.1002/chin.199543318
https://doi.org/10.1002/chin.199543318
Autor:
C. F. Marth, Edwin Vedejs
Publikováno v:
Journal of the American Chemical Society. 112:3905-3909
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::854f815e4ca6650a5e85181002fa1d09
https://doi.org/10.1021/ja00166a026
https://doi.org/10.1021/ja00166a026
Publikováno v:
Magnetic Resonance in Chemistry. 28:559-560
The results of 47/49Ti NMR measurements on 21 organotitanium compounds are reported. A signal could be detected for only about half of the compounds measured. Methyltitanium trichloride is highly deshielded compared with TiCl4.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66b88124231a92f2d828afb68e7f806e
https://doi.org/10.1002/mrc.1260280617
https://doi.org/10.1002/mrc.1260280617
Publikováno v:
Journal of the American Chemical Society. 110:3940-3948
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f94ee56a6eb95d0e10eaaecb9f04265a
https://doi.org/10.1021/ja00220a036
https://doi.org/10.1021/ja00220a036
Autor:
C. F. Marth, E. Vedejs
Publikováno v:
Journal of the American Chemical Society. 110:3948-3958
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b225b93236d8a2f2267bb1edac551f69
https://doi.org/10.1021/ja00220a037
https://doi.org/10.1021/ja00220a037
Autor:
Edwin Vedejs, C. F. Marth
Publikováno v:
Tetrahedron Letters. 28:3445-3448
Phosphorus ylides based on the dibenzophosphole (DBP) ring system convert aldehydes into trans-disubstituted oxaphosphetanes with good to excellent selectivity. Decomposition at 70–110° affords alkenes with E:Z ratios from 6:1 to > 100:1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32df11ccd02ec709b5d54d71bbd02ef7
https://doi.org/10.1016/s0040-4039(00)96322-6
https://doi.org/10.1016/s0040-4039(00)96322-6
Autor:
E. Vedejs, C. F. Marth
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::328b1c6288496d3b6fc8824b757d1dbb
https://doi.org/10.1002/chin.198840117
https://doi.org/10.1002/chin.198840117
Publikováno v:
ChemInform. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a1d453c46165b80b4122026524719f6
https://doi.org/10.1002/chin.198840122
https://doi.org/10.1002/chin.198840122
Autor:
Edwin Vedejs, C. F. Marth
Publikováno v:
ChemInform. 18
Phosphorus ylides based on the dibenzophosphole (DBP) ring system convert aldehydes into trans-disubstituted oxaphosphetanes with good to excellent selectivity. Decomposition at 70–110° affords alkenes with E:Z ratios from 6:1 to > 100:1.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e95b2eeb3d134c4dded91befa4c4984
https://doi.org/10.1002/chin.198752127
https://doi.org/10.1002/chin.198752127