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Bush CE Goldston RJ Scott SD Fredrickson ED McGuire K Schivell J Taylor G Barnes CW Bell MG Boivin RL Bretz N Budny RV Cavallo A Efthimion PC Grek B Hawryluk R Hill K Hulse RA Janos A Johnson DW Kilpatrick S Manos DM Mansfield DK Meade DM Park H Ramsey AT Stratton B Synakowski EJ Towner HH Wieland RM Zarnstorff MC Zweben S 《Physical review letters》1990,65(4):424-427
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Chen D Albuquerque IF Baublis VV Bondar NF Carrigan RA Cooper PS Lisheng D Denisov AS Dobrovolsky AV Dubbs T Endler AM Escobar CO Foucher M Golovtsov VL Goritchev PA Gottschalk H Gouffon P Grachev VT Khanzadeev AV Kubantsev MA Kuropatkin NP Lach J Lang Pengfei Lebedenko VN Li Chengze Li Yunshan Mahon JR McCliment E Morelos A Newsom C Pommot Maia MC Samsonov VM Schegelsky VA Shi Huanzhang Smith VJ Sun CR Tang Fukun Terentyev NK Timm S Tkatch II Uvarov LN Vorobyov AA Yan Jie Zhao Wenheng 《Physical review letters》1992,69(23):3286-3289
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Foucher M Albuquerque IF Bondar NF Carrigan R Chen D Li Chengze Cooper PS Denisov AS Dobrovolsky AV Dubbs T Endler AM Escobar CO Tang Fukun Golovtsov VL Goritchev PA Gottschalk H Gouffon P Grachev VT Shi Huanzhang Yan Jie Khanzadeev AV Kubantsev MA Kuropatkin NP Lach J Luksys M Lebedenko VN Dai Lisheng Mahon JR McCliment E Morelos A Newsom C Lang Pengfei Pommot Maia MC Samsonov VM Zheng Shuchen Smith VJ Terentyev NK Timm S Tkatch II Uvarov LN Vorobyov AA Zhao Wenheng Zhong Yuanyuan 《Physical review letters》1992,68(20):3004-3007
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Robert M. Adlington Jack E. Baldwin William MC Coull Gareth J. Pritchard Christopher J. Schofield Nicholas J. Westwood 《合成通讯》2013,43(21):3803-3813
N-Arylsulfonylation of 2-azetidinones can lead to the diastereoselective formation of oligomerization products. However, a simple increase of arylsulfonyl chloride concentration minimized oligomerization and allowed preparation of 1-arylsulfonyl-2-azetidinones in good yield. 相似文献