jo8b00728_si_002.cif (747.67 kB)
Evolution of a Strategy for the Enantioselective Total Synthesis of (+)-Psiguadial B
datasetposted on 2018-05-04, 00:00 authored by Lauren M. Chapman, Jordan C. Beck, Caitlin R. Lacker, Linglin Wu, Sarah E. Reisman
(+)-Psiguadial B is a diformyl phloroglucinol meroterpenoid that exhibits antiproliferative activity against the HepG2 human hepatoma cancer cell line. This full account details the evolution of a strategy that culminated in the first enantioselective total synthesis of (+)-psiguadial B. A key feature of the synthesis is the construction of the trans-cyclobutane motif by a Wolff rearrangement with in situ catalytic, asymmetric trapping of the ketene. An investigation of the substrate scope of this method to prepare enantioenriched 8-aminoquinolinamides is disclosed. Three routes toward (+)-psiguadial B were evaluated that featured the following key steps: (1) an ortho-quinone methide hetero-Diels–Alder cycloaddition to prepare the chroman framework, (2) a Prins cyclization to form the bridging bicyclo[4.3.1]decane system, and (3) a modified Norrish–Yang cyclization to generate the chroman. Ultimately, the successful strategy employed a ring-closing metathesis to form the seven-membered ring and an intramolecular O-arylation reaction to complete the polycyclic framework of the natural product.
psiguadialenantioenriched 8- aminoquinolinamidessubstrate scopeNorrishSynthesidiformylexhibits antiproliferative activitypolycyclic frameworkaccount detailsevolutiontranseven-membered ringbicyclointramolecular Oinvestigationmethodhetero-Dielhepatoma cancer cell linemeroketenestrategyring-closingarylation reactionsynthesisconstructionphloroglucinolWolff rearrangementmetaPsiguadialEnantioselectivemotifStrategymethidechroman frameworkPrins cyclizationcycloquinoneorthoHepG 2