Asymmetric synthesis of 1,4-dideoxy-1,4-imino-d-ribitol via stereoselective addition of allylphenylsulfone to an aryl N-sulfinylimine |
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| Institution: | 1. Department of Mechanical Engineering, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 32610 Tronoh, Perak, Malaysia;2. Facultatea Stiinta si Ingineria Materialelor, Universitatea Tehnica \"Gheorghe Asachi\" din Iasi, IASI, Romania;3. Center for Energy Studies, Department of Mechanical Engineering, JNTUH College of Engineering, Kukatpally, 500085 Hyderabad, Telangana, India;1. Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi 214122, Jiangsu, China;2. State Key Laboratory of Food Science & Technology, Wuxi 214122, Jiangsu, China;1. Department of Physics, National Dong Hwa University, Hualien 97401, Taiwan;2. Department of Physics, Savitribai Phule Pune University (Formerly University of Pune), Pune 411007, India;3. Institute of Physics, Academia Sinica, Taipei 11529, Taiwan |
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| Abstract: | Asymmetric synthesis of 1,4-dideoxy-1,4-imino-d-ribitol was achieved utilizing the stereoselective addition of allylphenylsulfone to a chiral N-sulfinyl-2-furfuryl imine and ring-closing metathesis reactions as key steps. |
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