Oxidative ring transformation of 2-furylcarbinols in natural product syntheses
作者： Toshio Honda
DOI: 10.1016/S1572-5995(96)80013-5
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摘要: Summary The stereoselective synthesis of variuos types natural poducts including steroids, alkaloids, and antibiotics, was successfully achieved in optically active forms by utilization the oxidative ring transformation 2-furylcarbinols to corresponding pyranones as key step. strategy for also reviewed.
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