Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Rivka Alkabets"'
Publikováno v:
The Journal of Organic Chemistry. 41:3682-3687
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a93f2e82307da42ce97ba7ad00caafe
https://doi.org/10.1021/jo00885a006
https://doi.org/10.1021/jo00885a006
Publikováno v:
The Journal of Organic Chemistry. 40:2304-2307
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53f5f978dec7548711cfe57e48fed404
https://doi.org/10.1021/jo00904a008
https://doi.org/10.1021/jo00904a008
Publikováno v:
Chemischer Informationsdienst. 6
2,2-Diarylpropanes are conveniently prepared from 1,1-diarylethylenes, lithium aluminium hydride, and anisole in tetrahydrofuran while 1,1-diarylethanes are obtained at 140 °C in bis(methoxyethyl) ether; hydride addition to 1,1-diarylethylenes is de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce3df7d93192aaf8af7f452f751b667a
https://doi.org/10.1002/chin.197531217
https://doi.org/10.1002/chin.197531217
Publikováno v:
ACS Symposium Series ISBN: 9780841206632
Phosphorus Chemistry: Proceedings of the 1981 International Conference
Phosphorus Chemistry: Proceedings of the 1981 International Conference
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33f4a95ecd2f36305380e5b7ba0372f7
https://doi.org/10.1021/bk-1981-0171.ch089
https://doi.org/10.1021/bk-1981-0171.ch089
Publikováno v:
Chemischer Informationsdienst. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d12a14254e000d6cf0163b3c421c0e45
https://doi.org/10.1002/chin.197814285
https://doi.org/10.1002/chin.197814285
Publikováno v:
Chemischer Informationsdienst. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f556d2b3f2df36f0c7310cff188fed02
https://doi.org/10.1002/chin.197547289
https://doi.org/10.1002/chin.197547289
Publikováno v:
Chemischer Informationsdienst. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f1ef79ed57dcfa75640aa5a0f8c1685
https://doi.org/10.1002/chin.198143259
https://doi.org/10.1002/chin.198143259
Publikováno v:
J. Chem. Soc., Chem. Commun.. :348-349
2,2-Diarylpropanes are conveniently prepared from 1,1-diarylethylenes, lithium aluminium hydride, and anisole in tetrahydrofuran while 1,1-diarylethanes are obtained at 140 °C in bis(methoxyethyl) ether; hydride addition to 1,1-diarylethylenes is de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1e04072c453f72db0f7be9a70951af2
https://doi.org/10.1039/c39750000348
https://doi.org/10.1039/c39750000348
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :981
Deprotonation of the alcohol (2) gives the phosphorane oxide anion (3) which equilibrates with its exceptionally reactive tautomeric phosphine oxide alkoxide (4).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8374186664953c8a03d9d38d665a3c1e
https://doi.org/10.1039/c39810000981
https://doi.org/10.1039/c39810000981
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :622
The title reaction gives the novel acyloxy-chlorophosphorane (1) and the analogous fluoride (9) is similarly obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcb3c868d6f7fe3dd1b4c6e52ea35c42
https://doi.org/10.1039/c39810000622
https://doi.org/10.1039/c39810000622