Enantioselective and Protecting Group-Free Synthesis of 1-Deoxythionojirimycin, 1-Deoxythiomannojirimycin, and 1-Deoxythiotalonojirimycin
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https://figshare.com/articles/dataset/Enantioselective_and_Protecting_Group_Free_Synthesis_of_1_Deoxythionojirimycin_1_Deoxythiomannojirimycin_and_1_Deoxythiotalonojirimycin/2725465
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资源简介：
1-Deoxythioglyconojirimycins were synthesized by using a protecting group-free strategy, starting from readily available carbohydrates, in good overall yield. Use of benzyltriethylammonium tetrathiomolybdate, [BnEt3N]2MoS4, as a sulfur transfer reagent and borohydride exchange resin (BER) reduction of a lactone enabled the efficient synthesis of the title compounds.
创建时间：
2010-10-01
