386211-68-3Relevant articles and documents
Concise enantioselective syntheses of quinolactacins A and B through alternative winterfeldt oxidation
Zhang, Xuqing,Jiang, Weiqin,Sui, Zhihua
, p. 4523 - 4526 (2003)
Enantioselective total syntheses of (+)-quinolactacin B and (+)-quinolactacin A2 through asymmetric Pictet-Spengler cyclization and KO2 oxidation-an alternative Winterfeldt condition-are described.
Engineered Biosynthesis of Fungal 4-Quinolone Natural Products
Liu, Mengting,Ohashi, Masao,Tang, Yi
supporting information, p. 6637 - 6641 (2020/09/02)
Quinolone-containing natural products are widely found in bacteria, fungi, and plants. The fungal quinolactacins, which are N-methyl-4-quinolones, display a wide spectrum of biological activities. Here we uncovered a concise nonribosomal peptide synthetase pathway involved in quinolactacin A biosynthesis from Penicillium by using heterologous reconstitution and in vitro enzymatic synthesis. The N-desmethyl analog of quinolactacin A was accessed through the construction of a hybrid bacterial and fungi pathway in the heterologous host.