38156-66-0Relevant articles and documents
Total Synthesis of Aurofusarin: Studies on the Atropisomeric Stability of Bis-Naphthoquinones
Qi, Chao,Wang, Wenyu,Reichl, Kyle D.,McNeely, James,Porco, John A.
supporting information, p. 2101 - 2104 (2018/02/06)
An efficient annulation involving pyrone addition to a quinone and Dieckmann condensation was developed for rapid assembly of a γ-naphthopyrone monomeric precursor to the bis-naphthoquinone natural product aurofusarin. Dimerization was achieved through Pd
Evaluation of some preparations of trialkoxyphthalic acid derivatives
Parker, Kathlyn A.,Spero, Denice M.,Koziski, Kathleen A.
, p. 183 - 188 (2007/10/02)
Several approaches to trialkoxyphthalic acid derivatives, potential intermediates in a fredericamycin synthesis, were tested. Sequences based on a Diels-Alder/retro Diels-Alder reaction, a cyanide addition to a quinone, an Elbe oxidation, and an amide-directed ortho-lithiation are discussed in terms of length, yields, convenience, and the versatility of the product of each.