Katalitik assimetrik Diels-Alder reaktsiyalari asosan Lyuis kislotasi katalizatorlari
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Eslatmalar va havolalar 19- sen tab r 20 1 4- yil d a e ÿl o n q i ling a n. M a hid ol u niversite ti t omon ida n 02 .03 .2 01 5 05 :34 :5 8 da yukla ng an . ChemComm Aloqa 1 Enantioselektiv Diels-Alder reaktsiyalarining sharhlari uchun qarang: (a) W. Oppolzer, Comprehensive Organic Synthesis, ed. BM Trost, Pergamon Press, Nyu-York, 1991, jild. 5; (b) R. Noyori, Organik sintezdagi assimetrik katalizatorlar, Wiley, Nyu-York, 1994; (c) H. Yamamoto, Lyuis kislotasi reagentlari, Kimyo. Kommun., 2014, 50, 14113--14116 | 14115 Ushbu jurnal © The Royal Society of Chemistry 2014 Machine Translated by Google Ushbu jurnal © The Royal Society of Chemistry 2014 14116 | Kimyo. Kommun., 2014, 50, 14113--14116 19- sen tab r 20 1 4- yil d a e ÿl o n q i ling a n. M a hid ol u niversite ti t omon ida n 02 .03 .2 01 5 05 :34 :5 8 da yukla ng an . Maqolani onlayn ko'rish 17 CCDC 1000789. 4 RS Singx va T. Xarada, Evr. J. Org. Kimyo., 2005, 3433. ChemComm 18 M. Rueping, BJ Nachtsheim, RM Koenigs va W. Ieawsuwan, Chem. - Yevro. J., 2010, 16, 1311. Oksford universiteti nashriyoti, Oksford, 1999; (d) DA Evans va JS Jonson, keng qamrovli assimetrik katalizda, nashr. EN Jacobsen, A. Pfaltz va X. Yamamoto, Springer, Nyu-York, 1999, jild. 3, p. 1177; (e) S. Reymond va J. Kossi, Chem. Rev., 2008, 108, 5359; ( f ) LC Dias, J. Braz. Kimyo. 5 D. Nakashima va X. Yamamoto, J. Am. Kimyo. Soc., 2006, 128, 9626. 8 (a) M. Rueping, A. Kuenkel va I. Atodiresei, Chem. Soc. Rev., 2011, 40, 4539; (b) M. Rueping, V. Ieawsuwan, AP Antonchick va Soc., 1997, 8, 289; (g) HB Kagan va O. Riant, Chem. Rev., 1992, 92, 1007; (h) X. Jiang va R. Vang, Chem. Rev., 2013, 113, 5515; (i) Y. Ding, C. Chjan va V. Xua, Chin. J. Org. Chem., 2003, 23, 1076. 6 Chiral fosfor kislotasi va fosfat katalizlangan assimetrik Diels-Alder reaktsiyalari uchun qarang: (a) J. Itoh, K. Fuchibe va T. Akiyama, Angew. Chem., Int. Ad., 2006, 45, 4796; (b) T. Akiyama, X. Morita va K. Fuchibe, J. Am. Kimyo. Soc., 2006, 128, 13070; (c) N. Momiyama, X. Tabuse va M. Terada, J. Am. Kimyo. Soc., 2009, 131, 12882; (d) N. Momiyama, T. Konno, Y. Furiya, T. Iwamoto va M. Terada, J. Am. Kimyo. Soc., 2011, 133, 19294; (e) G. Li, T. Liang, L. Voytas va JC Antilla, Anjyu. Chem., Int. Nashr, 2013 yil, 52, 4628; ( f ) X. Tian, N. Xofman va P. Melkior, Anjyu. Chem., Int. Ad., 2014, 53, 2997; (g) M. Rueping va S. Raja, Beylshteyn J. Org. Chem., 2012, 8, 1819; (h) J. Lv, X. Zhong, J.-P. Cheng va S. Luo, Huaxue Xuebao, 2012, 70, 1518. 7 (a) P. Jiao, D. Nakashima va X. Yamamoto, Angew. Chem., Int. Ad., 2008, 47, 2411; (b) CH Cheon va X. Yamamoto, J. Am. Kimyo. Soc., 2008, 130, 9246; (c) CH Cheon va H. Yamamoto, Org. Lett., 2010, 12, 2476. 2 AB Northrup va DWC MacMillan, J. Am. Kimyo. Soc., 2002, 13 (a) LE Overman va PJ Jessup, J. Am. Kimyo. Soc., 1978, 100, 5179; (b) LE Overman, CB Petty va RJ Doedens, J. Org. Chem., 1979, 44, 4183; (c) LE Overman, RL Freerks, CB Petty, LA Clizbe, RK Ono, CF Taylor va PJ Jessup, J. Am. Kimyo. Soc., 1981, 103, 2816; (d) LE Overman, CB Petty, T. Ban va GT Huang, J. Am. Kimyo. Soc., 1983, 105, 6335. BJ Nachtsheim, Anjyu. Chem., Int. Ad., 2007, 46, 2097; (c) M. Rueping, BJ Nachtsheim, SA Moreth va M. Bolte, Anjew. Chem., Int. Ad., 2008, 47, 593; (d) M. Rueping, T. Theissmann, A. Kuenkel va RM Koenigs, Anjew. Chem., Int. Ad., 2008, 47, 6798; (e) M. Rueping va V. Ieawsuwan, Adv. Sint. Catal., 2009, 351, 78. 9 (a) M. Zeng, Q. Kang, QL He va SL You, Adv. Sint. Katal., 2008, 350, 2169; (b) Z. Feng, QL Xu, LX Dai va SL You, Heterocycles, 2010, 80, 765; (c) Z. Feng, M. Zeng, QL Xu va SL Siz, Chin. Sci. 14 1 mmol EVK va 2 mmol karbamat bitta idishda reaksiyaga kirishdi. Bull., 2010, 55, 1723. 10 (a) I. Cÿoric´ va B. List, Nature, 2012, 483, 315; (b) S. Liao, I. Cÿoric´, Q. Vang va B. List, J. Am. Kimyo. Soc., 2012, 134, 10765; (c) S. Vellalat, I. Cÿoric´ va B. List, Anjyu. Chem., Int. Nashr, 2010, 49, 9749. 5 soat davomida. 11 K. Vu, YJ Jiang, YS Fan, D. Sha va SQ Zhang, Chem. - Yevro. J., 2013, 19, 474. 12 (a) DA Evans, DM Barnes, JS Jonson, T. Lectka, P. von Matt, SJ Miller, JA Murry, RD Norcross, EA Shaughnessy va KR Campos, J. Am. Kimyo. Soc., 1999, 121, 7582; (b) P. Wipf va X. Vang, Tetrahedron Lett., 2000, 41, 8747; (c) Y. Huang, T. Ivama va VH Raval, J. Am. Kimyo. Soc., 2000, 122, 7843; (d) SA Kozmin, Y. Huang, T. Iwama va VH Rawal, J. Am. Kimyo. Soc., 2002, 124, 4628; (e) Y. Xuang, T. Ivama va VH Raval, J. Am. Kimyo. Soc., 2002, 124, 5950. 15 Tafsilotlar uchun ESI† ga qarang. 124, 2458. 16 Y. Huang, T. Iwama va VH Rawal, Org. Lett., 2002, 4, 1163. Aloqa 3 (a) EJ Kori, Anjyu. Chem., Int. Ed., 2009, 48, 2100; (b) DH Ryu, TW Li va EJ Kori, J. Am. Kimyo. Soc., 2002, 124, 9992; (c) DH Ryu va EJ Kori, J. Am. Kimyo. Soc., 2003, 125, 6388; (d) DH Ryu, G. Zhoug va EJ Kori, J. Am. Kimyo. Soc., 2004, 126, 4800; (e) D. Liu, E. Kanales va EJ Kori, J. Am. Kimyo. Soc., 2007, 129, 1498. Machine Translated by Google Download 84.95 Kb. Do'stlaringiz bilan baham: |
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