87402-50-4Relevant academic research and scientific papers
Highly diastereoselective tandem photoenolization-hetero-Diels-Alder cycloaddition reactions of o-tolualdehydes in the solid state
Moorthy, Jarugu Narasimha,Mal, Prasenjit,Singhal, Nidhi,Venkatakrishnan, Parthasarathi,Malik, Ravish,Venugopalan, Paloth
, p. 8459 - 8466 (2007/10/03)
The (E)-photoenols generated in situ by photolysis of o-tolualdehydes 1-5 in the solid state react with the precursor aldehydes as dienophiles in a hetero-Diels-Alder cycloaddition fashion to afford trans-3-arylisochromanols in excellent yields and in a h
Electron Donor-Acceptor Compounds, XXX. Electron Donor-Acceptor Paracyclophanes with N,N,N',N'-Tetramethyl-p-phenylenediamine (TMPD) as Donor Unit
Staab, Heinz A.,Reimann-Haas, Renate,Ulrich, Peter,Krieger, Claus
, p. 2808 - 2826 (2007/10/02)
The donor-acceptor paracyclophanes 1 and 2 which contain N,N,N',N'-tetramethyl-p-phenylenediamine (TMPD) as donor component were synthesized: starting from the paracyclophanes 5 and 6 via 7, 9, 11 and 8, 10, 12, resp., the two diastereomeric TMP
