期刊
Organic Chemistry Frontiers
卷 1, 期 8, 页码 974-982出版社
CHINESE CHEMICAL SOC
DOI: 10.1039/c4qo00142g
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资金
- Natural Sciences and Engineering Research Council of Canada (NSERC)
- Fonds Quebecois de la Recherche sur la Nature et les Technologies (FQRNT)
Reported herein is the synthesis of all possible stereotriad propionates derived from L-lactic acid and L-alanine. The approach is based on a stereocontrolled Mukaiyama aldol reaction followed by a free radical-mediated hydrogen transfer, for which the choice of Lewis acid (monodentate or bidentate) dictates the stereochemical outcome in each reaction. The sequential process has been applied iteratively for the synthesis of eight stereopentad motifs derived from beta,gamma-alkoxyaldehydes. New experimental data and DFT calculations (BHandHLYP/TZVP) of the transition states involved in the radical reduction of aluminate intermediates support the proposed model of the endocyclic effect leading to high 2,3-syn selectivities for the synthesis of propionates and subunits thereof.
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