全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
化学进展  2014 

非官能化烯烃的不对称催化环氧化反应

DOI: 10.7536/PC140732, PP. 1942-1961

Keywords: 非官能化烯烃,不对称催化环氧化,酶催化剂,金属卟啉,金属Salen配合物,有机催化剂,催化机理

Full-Text   Cite this paper   Add to My Lib

Abstract:

手性环氧化合物是有机合成的重要中间体,由于三元杂环的张力使其很容易与各种亲核试剂作用,通过官能团转化反应,可以从环氧化物制备一系列不同结构的手性化合物.烯烃的不对称环氧化反应可以使潜手性的烯烃转化为带有手性碳的环氧化合物,在医药、农药、香料等精细化学品的合成上具有非常重要的意义.非官能化烯烃经手性催化剂诱导的不对称环氧化反应是获得光学纯手性化合物的有效方法.这些手性催化剂包括生物酶、金属卟啉、金属Salen配合物以及有机小分子催化剂.本文综述了这几种催化剂催化的非官能化烯烃不对称催化环氧化反应近几年的研究进展,介绍了催化剂的催化机理,并就其发展趋势提出了构想.

References

[1]  Kubo T, Peters M W, Meinhold P, Amold F H. Chemistry, 2006, 12: 1216.
[2]  吴襟(Wu J), 孙万儒(Sun W R). 生物工程进展(Progress in Biotechnology), 2001, 21(4): 234.
[3]  Poulos T L, Raag R. Faseb. J., 1992, 6: 674.
[4]  Raag R, Poulos T L. Biochemistry, 1991, 30: 2674.
[5]  李亚非(Li Y F), 王繁业(Wang F Y). 化学工业与工程技术(Journal of Chemical Industry & Engineering), 2007, 27(6):44.
[6]  Bernasconi S, Orsini F, Sello G, Colmegna A, Galli E, Bestetti G. Tetrahedron Lett., 2000, 41: 9157.
[7]  Panke S, Wubbolts M. G, Schmid A, Witholt B. Biotechnol. Bioeng., 2000, 69: 91.
[8]  Bernasconi S, Orsini F, Sello G, Di Gennaro P. Tetrahedron: Asymmetry, 2004, 15: 1603.
[9]  Park S M, Bae J W, Han J H, Lee E Y, Lee S G, Park S J. Microbiol. Biotechnol., 2006, 16: 1041.
[10]  Kuhn D, Kholiq M A, Heinzle E, Buhler B. Schmid A. Green Chem., 2010, 12: 815.
[11]  Panke S, Held M, Wubbolts M G, Witholt B, Schmid A. Biotechnol. Bioeng., 2002, 80: 33.
[12]  Hofstetter K, Lutz J, Lang I, Witholt B, Schmid A. Angew. Chem. Int. Ed., 2004, 43: 2163.
[13]  Hollmann F, Hofstetter K, Habicher T, Hauer B, Schmid A. J. Am. Chem. Soc., 2005, 127: 6540.
[14]  Lin H, Liu Y, Wu Z L. Chem. Commun., 2011, 47: 2610.
[15]  Zhang R, Yu W Y, Wong K Y, Che C M. J. Org. Chem., 2001, 66: 8145.
[16]  Niwa T, Nakada M. J. Am. Chem. Soc., 2012, 134: 13538.
[17]  Dai W, Li J, Li G S, Yang H, Wang L Y, Gao S. Org. Lett., 2013, 15: 4138.
[18]  Irie R, Noda K, Ito Y, Katsuki T. Tetrahedron Lett., 1990, 31: 7345.
[19]  Lee N H, Muci A R, Jacobsen E N. Tetrahedron Lett., 1991, 32: 5055.
[20]  Deng L, Jacobsen E N J. Org. Chem., 1992, 57: 4320.
[21]  Chang S, Lee N H, Jacobsen E N. J. Org. Chem., 1993, 58: 6939.
[22]  Chang S, Galvin J M, Jacobsen E N. J. Am. Chem. Soc., 1994, 116: 6937.
[23]  Brandes B D, Jacobsen E N. J. Org. Chem., 1994, 59: 4378.
[24]  Palucki M, Pospisil P J, Zhang W, Jacobsen E N. J. Am. Chem. Soc., 1994, 116: 9333.
[25]  Brandes B D, Jacobsen E N. Tetrahedron Lett., 1995, 36: 5123.
[26]  Liao S H, List B. Angew. Chem. Int. Ed., 2010, 49: 628.
[27]  林晓倩(Lin X Q), 卢楠(Lu N), 山东化工(Shandong Chemical Industry), 2011, 40(1):34.
[28]  Yang D. Acc. Chem. Rev., 2004, 37: 497.
[29]  Ma S M. Topics in Organometallic Chemistry. Berlin Heidelberg: Springer-Verlag, 2011. 123.
[30]  [161 Wong O A, Shi Y. Chem. Rev., 2008, 108: 3958.
[31]  Bohe L, Hanquet G, Lusinchi M, Lusinchi X. Tetrahedron Lett., 1993, 34:7271.
[32]  Bohe L, Lusinchi M, Lusinchi X. Tetrahedron, 1999, 55: 141.
[33]  Page P C B, Buckley B R, Heaney H, Blacker A J, Org. Lett., 2005, 7: 375.
[34]  Farahb M M, Bulman Page P C, Buckley B R, Blacker A J, Elsegood M R J. Tetrahedron, 2013, 69: 758. ?
[35]  Collins A N, Sheldrake G N, Crosby J. Chirality in Industry. NY: Wiley, 1992. 303.
[36]  Vries de E J, Janssen D B. Curr. Opin. Biotechnol., 2003, 14: 414.
[37]  Kasai N, Suzuki T, Furukawa Y. J. Mol. Catal. B: Enzyme, 1998, 4: 237.
[38]  王积涛(Wang J T), 陈蓉(Chen R), 冯霄(feng X), 李月明(Li Y M).有机化学(Chin. J. Org. Chem.), 1998, 18(2): 97.
[39]  王歆燕(Wang X Y), 石鸿昌(Shi H C), 徐寿颐(Xu S Y). 有机化学(Chin. J. Org. Chem.), 2001, 21(12): 1102.
[40]  周智明(Zhou Z M), 李连友(Li L Y), 徐巧(Xu Q), 徐从煊(Xu C X).有机化学(Chin. J. Org. Chem.), 2005,25(4):347.
[41]  罗云飞(Luo Y F), 邹晓川(Zou X C), 傅相锴(Fu X K), 贾紫永(Jia Z Y), 黄雪梅(Huang X M).中国科学:化学(Scientia Sinica Chimica), 2011, 41(3): 433.
[42]  张治国(Zhang Z G), 王歆燕(Wang X Y),孙川(Sun C),石鸿昌(Shi H C). 有机化学(Chin. J. Org. Chem.), 2004, 24(1): 7.
[43]  郑炎松(Zhen Y S),田振锋(Tian Z F). 化学通报(Chemistry), 2002, 65(4): 261.
[44]  王春(Wang C), 高勇军(Gao Y J), 张英群(Zhang Y Q), 王志(Wang Z), 马晶军(Ma J J). 化学进展(Progress in Chemistry), 2006, 18(6), 761.
[45]  Lee E Y, Shuler M L. Biotechnol. Bioeng., 2007, 98: 318.
[46]  Archelas A, Furstoss R. Curr. Opin. Chem. Biol., 2001, 5: 112.
[47]  Steinreiber A, Faber K. Curr. Opin. Biotechnol., 2001, 12: 552.
[48]  张玲玲(Zhang L L), 巴丽娜(Ba L N), 林章凛(Lin Z L), 朱玉山(Zhu Y S). 计算机与应用化学(Computers and Applied Chemistry), 2010, 1: 025.
[49]  Ortiz de Montellano P R, Fruetel J A, Collins J R, Camper D L, Loew G H. J. Am. Chem. Soc., 1991, 113: 3195.
[50]  Ruettinger R T, Fulco A J. J. Biol. Chem., 1981, 256: 5728.
[51]  Wistuba D, Nowotny H P, Trager O, Schurig V. Chirality, 1989, 1: 127.
[52]  Martinez C A, Stewart J D. Curr. Org. Chem., 2000, 4: 263.
[53]  van Deurzen M P J, van Rantwijk F, Sheldon R A. Tetrahedron, 1997, 53: 13183.
[54]  Colonna S, Gaggero N, Riehelmi C, Pasta P. Trends. Biotechnol., 1999, 17: 163.
[55]  Adam W, Lzarus M, Saha-Moller C R, Weiehold O, Hoch U, Haring D, Schreier P. Adv. Biochem. Eng. Biotechnol., 1999, 63: 73.
[56]  van Rantwijk F, Sheldon R A. Curr. Opin. Biotechnol., 2000, 11: 554.
[57]  智丽飞(Zhi L F), 蒋育澄(Jiang Y C), 胡满成(Hu M C), 李淑妮(Li S N). 化学进展(Progress in Chemistry), 2006, 18(9): 1150.
[58]  吴金跃(Wu J Y), 蒋育澄(Jiang Y C), 胡满成(Hu M C), 李淑妮(Li S N), 翟全国(Zhai Q G). 中国科学:化学(Scientia Sinica Chimica), 2010, 40(8): 1018.
[59]  Hager L P, Lakner F J. J. Mol. Catal. B: Enzym., 1998, 5: 95.
[60]  Hu S, Hager L P. Tetrahedron Lett., 1999, 40: 1641.
[61]  Hwang S, Choi C Y, Lee E Y. J. Ind. Eng. Chem., 2010, 16: 1.
[62]  方唯硕(Fang W S), 程克棣(Cheng K D). 有机化学(Chin. J. Org. Chem.), 2002, 22(10): 710.
[63]  Allain E J, Hager L P, Deng L, Jacobsen E N. J. Am. Chem. Soc., 1993, 115: 4415.
[64]  Dembitsky V M. Tetrahedron, 2003, 59: 4701.
[65]  Yi L, Steven M. Book of Abstracts, 219th ACS National Meeting, 2000.
[66]  Kazlauskas R J, Okrasa K. Chem. Eur. J., 2006, 12: 1587.
[67]  Keyhani J, Keyhani E, Zarchipour S, Tayefi-Nasrabadi H, Einollahi N. Biochem. Biophys. Acta, 2005, 1711: 312.
[68]  Zou P, Schrempf H. Eur. J. Biochem., 2000, 267: 2840.
[69]  刘雪英(Liu X Y), 刘军涛(Liu J T), 冯爱青(Feng A Q), 欧军(Ou J), 陈亿新(Chen Y X). 广州化工(Guangzhou Chemical Industry), 2006, 34(1): 16.
[70]  Guemgerich F P, Macdonald T L. Acc. Chem. Res. 1984, 17: 9.
[71]  周贤太(Zhou X T), 纪红兵(Ji H B), 裴丽霞(Pei L X), 佘远斌(She Y B), 徐建昌(Xu J C), 王乐夫(Wang Y F). 有机化学(Chin. J. Org. Chem.), 2007, 27(9): 1039.
[72]  王树军(Wang S J), 彭玉苓(Peng Y L). 化学进展(Progress in Chemistry), 2009, 21(7/8): 1515.
[73]  Gorves J T, Nemo T E. J. Am. Chem. Soc., 1983, 105: 5786.
[74]  Collman J P, Lee V J, Zhang X, Ibers J A, Brauman J I. J. Am. Chem. Soc., 1993, 115: 3834.
[75]  Collman J P, Zhang X, Lee V J, Brauman J L. J. Chem. Soc. Chem. Commun., 1992, 1647.
[76]  Che C M, Yu W Y. Pure Appl. Chem., 1999, 71: 281.
[77]  Collman J P, Wang Z, Straumanis A, Quelquejeu M, Rose E. J. Am. Chem. Soc., 1999, 121: 460.
[78]  任奇志(Ren Q Z), Rose E, Andrioletti B, 阎陶(Yan T). 化学学报(Acta Chimica Sinica), 2006, 64(24): 2447.
[79]  Ren Q Z, Hou Z S, Zhang H, Wang A Q, Liu S G. J. Porphyrins Phthalocyanines, 2009, 13: 1214.
[80]  Meunier B. Chem. Rev. 1992, 92: 1411.
[81]  Collman J P, Zhang X, Lee V J, Uffelman E S, Brauman J I. Science, 1993,261: 1404.
[82]  Oyama S T. Mechanisms in Homogeneous and Heterogeneous Epoxidation Catalysis. UK: Elsevier Science, 2008.
[83]  Garrison J M, Bruice T C. J. Am. Chem. Soc., 1989, 111:191.
[84]  Curet-Arana M C, Emberger G A, Broadbelt L J, Snurr R Q. J. Mol. Catal. A: Chem., 2008, 285: 120.
[85]  刘均洪(Liu J H), 梁辉(Liang H). 化学工业与工程技术(Journal of Chemical Industry & Engineering), 2007, 28(1): 6.
[86]  Zhang W, Loebach J L,Wilson S R, Jacobsen E N. J. Am. Chem. Soc., 1990, 112: 2801.
[87]  Huang X M, Fu X K, Wu X J, Jia Z Y. Tetrahedron Lett., 2013, 54: 4041.
[88]  Huang X M, Fu X K, Jia Z Y, Miao Q, Wang G M. Sci. China. Chem., 2013, 56: 604.
[89]  Suresh P, Srimurugan S, Dere T R, Venkat Ragavan R, Gopinath S V. Tetrahedron: Asymmetry, 2013, 24: 669.
[90]  Wang X, Miao C X, Wang S F, Xia C G, Sun W. ChemCatChem, 2013, 5: 2489.
[91]  Chen L H, Cheng F X, Jia L, Zhang A J, Wu J C, Tang N. Chirality, 2011, 23: 69.
[92]  Luo R C, Tan R, Peng Z G, Zheng W G, Kong Y, Yin D H. J. Catal., 2012, 287: 170.
[93]  Kuzniarska-Biernacka I, Silva A R, Carvalho A P, Pires J, Freire C. J. Mol. Catal. A: Chem., 2007, 278: 82.
[94]  Serrano D P, Vargas J A. Appl. Catal. A: Gen., 2008, 335: 172.
[95]  Sliva A R, Budarin V, Clark J H, Freire C, de Castro B. Carbon, 2007, 45: 1951.
[96]  屈育龙(Qu Y L), 胡道道(Hu D D). 高分子通报(Polymer Bulletin), 2005, 1: 31.
[97]  De B B, Lohray B B, Sivaram S, Dhal P. Tetrahedron: Asymmetry, 1995, 6: 2105.
[98]  Canali L, Cowan E, Deleuze H, Gibson C L, Sherrington D C. Chem. Commun., 1998, 2561.
[99]  Reger T S, Janda K D. J. Am. Chem. Soc., 2000, 122: 6929.
[100]  Beigi M, Haag R, Liese A. Adv. Synth. Catal., 2008, 350: 919.
[101]  Davis M E. Nature, 2002, 417: 813.
[102]  Mcmorn P, Huthings G J. Chem. Soc. Rev., 2004, 33: 108.
[103]  Frunza L, Kosslick H, Landmesser H, Hoft E, Fricke R. J. Mol. Catal. A: Chem., 1997, 123: 179.
[104]  Piaggio P, Langham C,ns: Oxidation). 北京:化学工业出版社(Beijing: Chemical Industry Press), 2008. 129.
[105]  Engelhardt U, Linker T. Chem. Commun., 2005, 1152.
[106]  Fu H, Look G C, Zhang W, Jacobsen E N, Wang C -H, J. Org. Chem., 1991, 56: 6497.
[107]  Norrby P -O, Linde C, ?kermark B. J. Am. Chem. Chem. Soc.,1995, 117: 11035.
[108]  B?ckvall J E, Bokman F, Blomberg M R A. J. Am. Chem. Chem. Soc., 1992, 114: 534
[109]  Adam W, Mock-Knoblauch C, Saha-M?ller C R, Herderich M. J. Am. Chem. Soc., 2000, 122: 9685.
[110]  [151 Adam W, Roschmann K J, Saha-M?ller C R, Seebach D J. Am. Chem. Soc., 2002, 124: 5068.
[111]  Bommarius A S, Riebel B R. Biocatalysis: Fundamentals and Applications. Wiley-VCH, 2004. 159.
[112]  Nnoyori R. Asymmetric Catalysis in Organic Synthesis. NY: Wiley, 1994. 137.
[113]  Dalko P I, Moisan L. Angew. Chem. Int. Ed., 2001, 40: 3726.
[114]  List B. Synlett., 2001, 1675.
[115]  Jarvo E R, Miller S J. Tetrahedron, 2002, 58: 2481.
[116]  张治国(Zhang Z G), 王歆燕(Wang X Y), 孙川(Sun C), 石鸿昌(Shi H C). 有机化学(Chin. J. Org. Chem.), 2004, 24(1):7.
[117]  Curci R, Fiorentino M, Serio M R. J. Chem. Soc., Chem. Commun., 1984 :155.
[118]  Curci R, Dinoi A, Rubino M F. Pure Appl. Chem., 1995, 67: 811.
[119]  Yang D, Yip Y C, Wang M K, Zheng J H. J. Am. Chem. Soc., 1996, 118: 491.
[120]  TuY, Wang Z, Shi Y. J. Am. Chem. Soc., 1996, 118: 9806.
[121]  Wang Z X, Tu Y, Frohn M, Zhang J R , Shi Y. J. Org. Chem., 1997, 62: 2328.
[122]  Frohn M, Shi Y. Synthesis, 2000, 1997.
[123]  Frohn M, Shi Y. Org. Synth., 2003, 80: 1.
[124]  Wong O A, Wang B, Zhao M X, Shi Y. J. Org. Chem., 2009, 74: 6335.
[125]  Denmark S E, Matsuhashi H. J. Org. Chem., 2002, 67: 3479.
[126]  [171 Vega-Pérez J M, Holm M V, Martínez M L, Blanco E, Iglesias-Guerra F. Eur. J. Org. Chem., 2009, 2009: 6009.
[127]  Aggarwal V K, Wang M F J. Chem. Soc., Chem. Commun., 1996, 191.
[128]  Page P C B, Rassias G A, Barros D, Ardakani A, Buckley B, Bethell D, SmithT A D, Slawin A M Z. J. Org. Chem., 2001, 66: 6926.
[129]  Page P C B, Buckley B R, Blacker A J. Org. Lett., 2004, 6: 1543.
[130]  Vachon J, Perollier C, Monchaud D, Marsol C, Ditrich K, Lacour J. J. Org. Chem.,2005, 70, 5903.
[131]  Page P C B, Buckley B R, Farah M M, Blacker A J, Eur. J. Org. Chem., 2009, 2009 : 3413.
[132]  Page P C B, Bartlett C J, Chan Y, Day D, Parker P, Buckley B R, Rassias G A, Slawin A M Z, Allin S M, Lacour J, Pinto A. J. Org. Chem., 2012, 77: 6128.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133