Rom ,-unsaturated esters has been created. The reaction sequence includes copper-catalyzed aminochlorination, aziridination and S N two nucleophilic ring-opening reaction. This one-pot reaction is operationally handy and may tolerate many different substratesAcknowledgementsWe gratefully acknowledge the financial support in the National Natural Science Foundation of China (No. 21102071)Scheme four: Proposed mechanism.Beilstein J. Org. Chem. 2014, 10, 1802?807.and also the Basic Study Funds for the Central Universities (No. 1107020522 and No. 1082020502). The Jiangsu 333 system (for Pan) and Changzhou Jin-Feng-Huang system (for Han) are also acknowledged.22. Soloshonok, V. A.; Ohkura, H.; Sorochinsky, A.; Voloshin, N.; Markovsky, A.; Belik, M.; Yamazaki, T. Tetrahedron Lett. 2002, 43, 5445?448. doi:ten.1016/S0040-4039(02)01103-6 23. de Figueiredo, R. M. Angew. Chem., Int. Ed. 2009, 48, 1190?193. doi:ten.1002/anie.200804362 24. Du, H.; Zhao, B.; Shi, Y. J. Am. Chem. Soc. 2007, 129, 762?63. doi:ten.1021/ja0680562 25. Mu z, K.; Nieger, M. Chem. Commun. 2005, 2729?731. doi:ten.1039/B502150B 26. Li, G.; Kim, S. H.; Wei, H.-X. Tetrahedron Lett. 2000, 41, 8699?703. doi:ten.1016/S0040-4039(00)01579-3 27. Li, G.; Wei, H.-X.; Kim, S. H.; Carducci, M. D. Angew. Chem., Int. Ed. 2001, 40, 4277?280. doi:10.1002/1521-3773(20011119)40:224277::AID-ANIE42773.0.CO ;2-I 28. Wu, H.; Ji, X.; Sun, H.; An, G.; Han, J.; Li, G.; Pan, Y. Tetrahedron 2010, 66, 4555?559. doi:10.1016/j.tet.2010.04.054 29. Li, G.; Saibabu Kotti, S. R. S.; Timmons, C. Eur. J. Org. Chem. 2007, 2745?758. doi:10.1002/ejoc.200600990 See to get a evaluation on aminohalogenation. 30. Han, J.-L.; Zhi, S.-J.; Wang, L.-Y.; Pan, Y.; Li, G. Eur. J. Org. Chem. 2007, 1332?337. doi:10.1002/ejoc.200600902 31. Mei, H.; Han, J.; Li, G.; Pan, Y. RSC Adv. 2011, 1, 429?33. doi:ten.1039/c1ra00174d 32. Li, G.; Wei, H.-X.; Kim, S. H.; Neighbors, M. Org. Lett. 1999, 1, 395?98. doi:10.1021/ol990059e 33. Chen, D.; Timmons, C.; Guo, L.; Xu, X.; Li, G. Synthesis 2004, 2479?484.849020-87-7 custom synthesis doi:10.1312941-98-2 structure 1055/s-2004-831203 34.PMID:27102143 Mei, H.; Yan, L.; Han, J.; Li, G.; Pan, Y. Chem. Biol. Drug Des. 2010, 76, 392?96. doi:ten.1111/j.1747-0285.2010.01023.x 35. Chen, D.; Guo, L.; Liu, J.; Kirtane, S.; Cannon, J. F.; Li, G. Org. Lett. 2005, 7, 921?24. doi:10.1021/ol050002u 36. Park, N. H.; Teverovskiy, G.; Buchwald, S. L. Org. Lett. 2014, 16, 220?23. doi:ten.1021/ol403209k 37. Boyall, D.; Frantz, D. E.; Carreira, E. M. Org. Lett. 2002, 4, 2605?606. doi:ten.1021/ol026282k 38. Soloshonok, V. A.; Ohkura, H.; Yasumoto, M. J. Fluorine Chem. 2006, 127, 924?29. doi:ten.1016/j.jfluchem.2006.04.003 39. Soloshonok, V. A.; Ohkura, H.; Yasumoto, M. J. Fluorine Chem. 2006, 127, 930?35. doi:10.1016/j.jfluchem.2006.04.
Action potential-independent spontaneous miniature neurotransmitter release has significant physiological functions including regulation of dendritic protein expression and maintenance of spines in glutamatergic synapses1, 2. Although `minis’ take place with out extracellular Ca2+ the majority of spontaneous release under physiological circumstances is Ca2+-dependent (e.g. refs.three, four). Unlike action potential-evoked release, that is triggered by transient activation ofUsers may view, print, copy, and download text and data-mine the content material in such documents, for the purposes of academic study, subject often for the full Situations of use:http://nature/authors/editorial_policies/license.html#terms �Present address: Department of Epileptology, University Clinics Bon.