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Rapidly diastereoselective assembly of ten-membered N-heterocycles between two 1,3-dipoles and their diversity to access fused N-heterocycles
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作者 Yan Luo Yan-Jiao Lu +6 位作者 Mei-Mei Pan Yu-Feng Liang Wei-Min Shi Chun-Hua Chen Cui Liang gui-fa su Dong-Liang Mo 《Chinese Chemical Letters》 2025年第5期211-217,共7页
The development of general and practical strategies toward the construction of medium-sized rings is still challenging in organic synthesis,especially for the multiple stereocenters control of substituted groups on th... The development of general and practical strategies toward the construction of medium-sized rings is still challenging in organic synthesis,especially for the multiple stereocenters control of substituted groups on the ring owing to the long distance between groups.Thus,stereoselective synthesis of multi-substituted ten-membered rings is attractive.Herein,a rapid assembly of various highly substituted ten-membered nitrogen heterocycles between two 1,3-dipoles through a tandem[3+3]cycloaddition/aza-Claisen rearrangement of N-vinyl-α,β-unsaturated nitrones and aza-oxyallyl or oxyallyl cations are disclosed.Products containing two or multiple stereocenters could be obtained in up to 96%yield with high regioselectivity and diastereoselectivity.Selective N-O bond cleavages of ten-membered nitrogen heterocycles lead to various novel 5,6,6-perifused benzofurans,bicyclo[4.4.0]or bicyclo[5.3.0]skeletons containing three or multiple continuous stereocenters in good yields and high diastereoselectivity.Biological tests show that the obtained ten-membered N-heterocycles and bicyclo[4.4.0]skeletons inhibited nitric oxide generation in LPS-stimulated RAW264.7 cells and might serve as good anti-inflammatory agents. 展开更多
关键词 1 3-Dipole Ten-membered N-heterocycles Aza-Claisen rearrangement [3+3]Cycloaddition NITRONE Anti-inflammatory
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