Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Liane Tikwe"'
Publikováno v:
Tetrahedron. 42:1693-1702
Triene 22 was synthesized and converted by two different routes to the tetraaldehyde 27, the first “non-bridged” derivative of 1. An X-ray analysis of 27 reveals that the CC bond is twisted by 28.6°. Attempts to prepare 1 from 27 failed, thus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c87701608fe9069f1f80b60378879227
https://doi.org/10.1016/s0040-4020(01)87586-4
https://doi.org/10.1016/s0040-4020(01)87586-4
Publikováno v:
Tetrahedron Letters. 26:1639-1642
The tetraaldehyde {=1} was synthesized by ozonation of the triene {=3}. The C=C-bond in {=1} is twisted by 28.6° and the CC-bond and the allylic bond lengths are significantly elongated to 135.7 and 155.5–159.7 pm, resp.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8959cc017a19b8426c6e45e736503726
https://doi.org/10.1016/s0040-4039(00)98572-1
https://doi.org/10.1016/s0040-4039(00)98572-1
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce7173378cc53fe94316243b813adaf0
https://doi.org/10.1002/chin.198631165
https://doi.org/10.1002/chin.198631165
Publikováno v:
Chemischer Informationsdienst. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2ed913336a20d1407591e10da70c869
https://doi.org/10.1002/chin.198531156
https://doi.org/10.1002/chin.198531156