7507-86-0Relevant articles and documents
Elaboration of the isochromane system of stephaoxocanes employing an Oxa-Pictet Spengler type cyclization
Kaufman, Teodoro S.,Bernardi, Carmem R.,Cipulli, Marcos,Silveira, Claudio C.
, p. 493 - 494 (2000)
An approach to the synthesis of the isochromane moiety embodying the AC-ring system of the stephaoxocanes, by the use of an Oxa-Pictet Spengler type cyclization strategy, is reported.
COMPOUNDS AND COMPOSITIONS FOR USE IN TREATING SKIN DISORDERS
-
Paragraph 0592; 0620-0622, (2021/08/06)
Provided herein is a compound of formula (XXXII) or a pharmaceutically acceptable salt, solvate, hydrate, stereoisomer thereof or a physiologically functional derivative thereof, wherein R1, R2, R3, G, A, E, n, p, and q are defined herein. Also provided herein are compositions comprising a compound of formula (XXXII), and methods of using a compound of formula (XXXII), e.g., in the treatment or prevention of skin disorders.
A novel donor-π-acceptor anthracene monomer: Towards faster and milder reversible dimerization
Van Damme, Jonas,van den Berg, Otto,Brancart, Joost,Van Assche, Guy,Du Prez, Filip
, p. 912 - 920 (2019/01/16)
A novel functional 2,6-substituted donor-acceptor anthracene derivative, bearing a long alkyl spacer and a polymerizable end-group, is synthesized from readily available compounds. This monomer possesses conjugated electron donor and acceptor moieties to achieve UV absorption and anthracene dimerization at higher wavelengths and under milder conditions, than anthracene and other reported anthracene derivatives. The compound was shown to absorb at higher wavelengths and dimerize much faster compared to most 9-substituted anthracenes. The fast photochemical and relatively slow thermal scission of the dimers were studied and related to the chemical structure, i.e. the 2,6-substitution.