13203-90-2Relevant articles and documents
Flow-vacuum pyrolysis of polycyclic compounds. 181 pyrolysis of 10,11-dIhydro-12H-dibenzo[a,d]cycloocten-5-ol
Parvulescu, Luminitza,Banciu, Anca,Pop, Mircea,Marton, George,Ciuculescu, Diana,Banciu, Mircea D.
, p. 725 - 731 (2007/10/03)
The flow-vacuum pyrolysis of 10,11-dihydro-12//-dibenzo[a,d]cycloocten-5-ol between 500-900°C and 1 mm Hg was investigated using GC/MS. Between 500°C and 700°C the unique reaction product is 10,11-dihydro-12H- dibenzo[a,d] cycloocten-5-one. At elevated te
The Effects of Stereochemistry of the Bridging Atoms in o-Substituted Arylbenzoic Acids on Root Antigravitropism
Teitei, Tsutomu
, p. 1461 - 1466 (2007/10/02)
Compounds in which an aryl or heteroaryl ring is linked to the ortho position of a benzoic acid moiety by a bridging group of up to four atoms are shown to inhibit the gravitropic response of cress seedling roots between 1E-5 and 1E-8 M.No significant difference in inhibitory activity is observed between compounds containing up to four saturated or two partially unsaturated bridging atoms, although analogues containing three or four partially unsaturated bridging atoms are one to two orders of magnitude more active.Compounds in which the aryl nuclei are fused together are shown to be inactive at the highest concentration tested.The results have been interpreted in terms of the aryl groups in the molecule interacting with a hypothetical receptor site, with the bridging atoms acting as a more or less flexible coupling to facilitate such interaction.
