116757-66-5Relevant articles and documents
Substituted heterocyclic compounds, method for preparing and compositions containing same
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, (2008/06/13)
The invention relates to compounds of formula (I): wherein: R1, R2and R3are as defined in the description, X is as defined in the description, Y represents an oxygen atom, a sulphur atom, a C(H)qgroup, SO or SO2, n is equal to from 0 to 5, A represents a NR5R6group, and medicinal products containing the same which are useful in treating or in preventing melatoninergic disorders.
Syntheses of 2-Substituted 6/7-Methoxy-1,4-benzodioxan-7/6-carbaldehydes
Taniguchi, Eiji,Yamauchi, Satoshi,Nagata, Shyuichirou,Ohnishi, Takeshi
, p. 630 - 635 (2007/10/02)
Five 2-substituted 6/7-methoxy-1,4-benzodioxan-7/6-carbaldehydes and 6-methoxy-1,4-benzodioxan-7-carbaldehyde available for the syntheses of insecticidal neolignan analogs were prepared from 4/3-benzyloxy-3/4-hydroxybenzaldehydes and 1,4-benzodioxan-6-carbaldehyde, respectively.
Synthese et proprietes biologiques photoinduites de dioxinnocoumarines lineaires
Guillaumet, Gerald,Hretani, Mohamed,Coudert, Gerard,Averbeck, Dietrich,Averbeck, Simone
, p. 45 - 51 (2007/10/02)
Synthesis and photoinduced biological properties of linear dioxinocoumarins.Several dioxinocoumarins with a substituted or unsubstituted coumarin moiety were synthesized from commercially available 6-amino-1,4-benzodioxan.Qualitative assays on the photoinduced inhibition of growth in the yeast Saccharomyces cerevisiae indicate that two dioxinocoumarins are photobiologically active. The 5H- benzopyranobenzodioxin-5-one 1d is more active than angelicin but less active than 8-MOP.The 9-methyl-7H-pyranobenzodioxin-7-one 1c is slightly less active than angelicin.
SYNTHESE D'UN ANALOGUE DIOXINIQUE DU PSORALENE
Guillaumet, G.,Hretani, M.,Coudert, G.
, p. 2665 - 2666 (2007/10/02)
The synthesis of a new analog of psoralen built on a benzodioxinic moiety have been efficiently achieved using as a key intermediate the 6-hydroxy 7-formyl 1,4-benzodioxan.