29445-64-5Relevant academic research and scientific papers
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
