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Building a small polypropionate library. Synthesis of all possible stereotetrads (building blocks for polyketide
O Arjona1, R Menchaca, J Plumet
1Departamento de Química Orgánica I, Facultad de Química, Universidad Complutense 28040-Madrid, Spain. plumety@eucmax.sim.ucm.es
The Journal of Organic Chemistry
|April 3, 2001
Abstract:
The all diastereomeric stereotetrads (polypropionate fragments) were synthesized in a stereodivergent fashion, starting from the Diels-Alder adducts of furan with acrylic acid and (-)-2-camphanoxyacrylonitrile, respectively. The key intermediates of these sequences were the oxanorbornenic sulfones 7, (-)-53 and (+)-54. Regio- and stereocontrolled alkylative ring opening of these intermediates afforded the cyclohexenyl sulfones 14, (+)-55 and (-)-58 which were transformed into the desired stereotetrads 30, 31, 40, 41, (+)-62, (+)-63, (-)-66, and (+)-69.