450357-58-1Relevant academic research and scientific papers
Convergent total synthesis of (±) myricanol, a cyclic natural diarylheptanoid
Bochicchio,Schiavo,Chiummiento,Lupattelli,Funicello,Hanquet,Choppin,Colobert
, p. 8859 - 8869 (2018/11/30)
Myricanol 1, a constituent of Myrica species, has been reported to lower the levels of the microtubule-associated protein tau (MAPT), whose accumulation plays an important role in some neurodegenerative diseases, such as Alzheimer's disease (AD). Herein w
Selective Claisen rearrangement and iodination for the synthesis of polyoxygenated allyl phenol derivatives
Bochicchio, Antonella,Cefola, Rossella,Choppin, Sabine,Colobert, Fran?oise,Di Noia, Maria Antonietta,Funicello, Maria,Hanquet, Gilles,Pisano, Isabella,Todisco, Simona,Chiummiento, Lucia
, p. 4053 - 4055 (2016/08/18)
Allyl aryl ethers and allyl phenol derivatives were prepared starting from commercial or synthetized phenols. Either Williamson reaction or Et2AlCl catalyzed Claisen rearrangement was performed to obtain the polyoxygenated molecules. The pivotal allyl phenols were then modified by methylation, iodocyclization or electrophilic aromatic iodination to afford the polyoxygenated derivatives in good to excellent yields. Additionally, their antibacterial properties were also investigated against Gram-positive and Gram-negative bacteria.
Complete π-facial diastereoselectivity in Diels-Alder reactions of dissymmetric 2,4-cyclohexadienones
Hou, Hui-Fang,Peddinti, Rama Krishna,Liao, Chun-Chen
, p. 2477 - 2480 (2007/10/03)
(Matrix presented) R = CH3 (b), CH=CH2 (c), ortho,endo.syn CH2CH=CH2 (d), Ph (e) predominant/major The studies in the Diels-Alder reactions of 5-methoxy-masked o-benzoquinone (1a, R = OMe) and simple dissymmetri
STRUCTURE-ACTIVITY RELATIONSHIPS OF PHENYLPROPANOIDS AS GROWTH INHIBITORS OF THE GREEN ALGA SELENASTRUM CAPRICORNUTUM
Greca, Marina Della,Monaco, Pietro,Pollio, Antonino,Previtera, Lucio
, p. 4119 - 4124 (2007/10/02)
Twenty-seven commercial or synthetic phenylpropanoids have been tested in broth against the unicellular alga Selenastrum capricornutum.The antialgal activity seems to be linked to the number as well as to the position of the methoxyl group in the molecule.A slight effect of the side chain substitution was also observed. Key Word Index - Selenastrum capricornutum; allelochemicals; phenylpropanoids.
