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  2010 

过渡金属催化的1,n-烯炔类化合物的不对称环异构化反应

, PP. 1341-1352

Keywords: 过渡金属催化,环异构化,烯炔化合物,不对称反应

Full-Text   Cite this paper   Add to My Lib

Abstract:

过渡金属催化的不对称环异构化反应催化活性高、选择性好,被认为是一条符合“原子经济性”的合成途径。近年来,该领域取得了长足的进步,成为构建高官能团活性的手性碳环与杂环化合物的最有效手段之一。本文比较全面地综述了20年来过渡金属催化的1,n-烯炔类化合物的不对称环异构化反应,并简单介绍了该反应在天然产物的合成过程中的应用。

References

[1]  [3 ] Lautens M,Klute W,Tam W. Chem. Rev. ,1996,96: 49—92
[2]  [4 ] Negishi E I,Coperet C,Ma S,et al. Chem. Rev. ,1996,96:
[3]  365—393
[4]  813—834
[5]  2180—2184
[6]  [9 ] Trost B M. Angew. Chem. Int. Ed. ,1995,34: 259—281
[7]  Trost B M. Acc. Chem. Res. ,1990,23: 34—42
[8]  96: 635—662
[9]  Fruehauf H W. Chem. Rev. ,1997,97: 523—596
[10]  Trost B M,Krische M J. Synlett,1998,1—16
[11]  Nakamura I,Yamamoto Y. Chem. Rev. ,2004,104: 2127—
[12]  2198
[13]  Anorbe L,Dominguez G,Perez-Castells J. Chem. Eur. J. ,
[14]  2004,10: 4938—4943
[15]  Trost B M,Lee D C,Rise F. Tetrahedron Lett. ,1989,30:
[16]  651—654
[17]  2001,40: 249—253
[18]  Hatano M, Mikami K. J. Am. Chem. Soc. , 2003, 125:
[19]  2003,2552—2555
[20]  Imase H,Suda T,Shibata Y,et al. Org. Lett. ,2009,11:
[21]  Jolly R S,Luedtke G,Sheehan D,et al. J. Am. Chem. Soc. ,
[22]  1990,112: 4965—4966
[23]  Wender P A,Takahashi H,Witulski B. J. Am. Chem. Soc. ,
[24]  1995,117: 4720—4721
[25]  Wender P A,Husfeld C O,Langkopf E,et al. J. Am. Chem.
[26]  Soc. ,1998,120: 1940—1941
[27]  Fairlie D P,Bosnich B. Organometallics,1988,7: 936—945
[28]  Tani K,Yamagata T,Akutagawa S,et al. J. Am. Chem. Soc. ,
[29]  Crabtree R. Acc. Chem. Res. ,1979,12: 331—337
[30]  207—257
[31]  Halpern J. Asymmetric Synth. ,1985,5: 41—69
[32]  Cao P,Wang B,Zhang X M. J. Am. Chem. Soc. ,2000,122:
[33]  Lei A W,He M,Wu S,et al. Angew. Chem. Int. Ed. ,2002,
[34]  41: 3457—3460
[35]  Lei A W,He M,Zhang X M. J. Am. Chem. Soc. ,2002,
[36]  124: 8198—8199
[37]  Liu F,Liu Q,He M,et al. Org. Biomol. Chem. ,2007,5:
[38]  3531—3534
[39]  He M,Lei A W,Zhang X M. Tetrahedron Lett. ,2005,46:
[40]  1823—1826
[41]  2003,345: 1237—1241
[42]  2004,346: 421—424
[43]  Mikami K,Kataoka S,Yusa Y,et al. Org. Lett. ,2004,6:
[44]  3699—3701
[45]  Gilbertson S R,Hoge G S,Genov D G. J. Org. Chem. ,1998,
[46]  Mamane V,Gress T,Krause H,et al. J. Am. Chem. Soc. ,
[47]  Brissy D,Skander M,Jullien H,et al. Org. Lett. ,2009,11:
[48]  Watson I D G,Ritter S,Toste F D. J. Am. Chem. Soc. ,
[49]  2009,131: 2056—2057
[50]  Worthen D M, Zimmerman T J, Wind C A. Invest.
[51]  Ophthalmol. ,1974,13: 296—299
[52]  358—361
[53]  Singh S B,Jayasuriya H,Ondeyka J G,et al. J. Am. Chem.
[54]  Ed. ,2007,46: 3942—3945
[55]  Porta A,Vidari G,Zanoni G. J. Org. Chem. ,2005,70:
[56]  De Azevedo M B M,Greene A E. J. Org. Chem. ,1995,60:
[57]  4940—4942
[58]  Vidari G, Lanfranchi G, Sartori P, et al. Tetrahedron:
[59]  3664—3666
[60]  Trost B M,Corte J R,Gudiksen M S. Angew. Chem. Int. Ed. ,
[61]  Trost B M,Czeskis B A. Tetrahedron Lett. ,1994,35: 211—
[62]  214
[63]  Goeke A,Sawamura M,Kuwano R,Ito Y. Angew. Chem. Int.
[64]  Ed. Engl. ,1996,35: 662—663
[65]  Zhang Q,Lu X Y. J. Am. Chem. Soc. ,2000,122: 7604—
[66]  7605
[67]  Zhang Q,Lu X Y,Han X. J. Org. Chem. ,2001,66: 7676—
[68]  7684
[69]  Hatano M,Terada M,Mikami K. Angew. Chem. Int. Ed. ,
[70]  4704—4705
[71]  Hatano M,Mikami K. J. Mol. Catal. A: Chem. ,2003,196:
[72]  165—169
[73]  Hatano M,Mikami K. Org. Biomol. Chem. ,2003,1: 3871—
[74]  3873
[75]  Hatano M,Yamanaka M,Mikami K. Eur. J. Org. Chem. ,
[76]  1805—1808
[77]  Koga Y,Kobayashi T,Narasaka K. Chem. Lett. ,1998,249—
[78]  250
[79]  1984,106: 5208—5217
[80]  Park J H,Chang K M,Chung Y K. Coord. Chem. Rev. ,
[81]  2009,253: 2461—2480
[82]  Perez-Castells J. Topics in Organometallic Chemistry,2006,19:
[83]  Gibson S E,Stevenazzi A. Angew. Chem. Int. Ed. ,2003,42:
[84]  1800—1810
[85]  Chi Y, Tang W, Zhang X M. Modern Rhodium-Catalyzed
[86]  Organic Reactions ( Ed. Evans P A) . Weinheim: Wiley-VCH,
[87]  2005. 1—31
[88]  Nass A R,Briel O. Chimica Oggi,2003,21: 58—61
[89]  6490—6491
[90]  Cao P, Zhang X M. Angew. Chem. Int. Ed. ,2000,39:
[91]  4104—4106
[92]  Lei A W,Waldkirch J P,He M,et al. Angew. Chem. Int.
[93]  Ed. ,2002,41: 4526—4529
[94]  Lei A W,He M,Zhang X M. J. Am. Chem. Soc. ,2003,
[95]  125: 11472—11473
[96]  Hashmi A S K,Haufe P,Nass A R. Adv. Synth. Catal. ,
[97]  Hashmi A S K,Haufe P,Nass A R,et al. Adv. Synth. Catal. ,
[98]  Mikami K,Yusa Y,Hatano M,et al. Chem. Commun. ,2004,98—99
[99]  Nicolaou K C,Li A,Ellery S P,et al. Angew. Chem. Int.
[100]  Ed. ,2009,48: 6293—6295
[101]  63: 10077—10080
[102]  2004,126: 8654—8655
[103]  Shibata T,Kobayashi Y,Maekawa S,et al. Tetrahedron,2005,
[104]  61: 9018—9024
[105]  2137—2139
[106]  Wang J,Soisson S M,Young K,et al. Nature,2006,441:
[107]  Soc. ,2006,128: 11916—11920
[108]  Nicolaou K C,Li A,Edmonds D J. Angew. Chem. Int. Ed. ,
[109]  2006,45: 7086—7090
[110]  Nicolaou K C,Edmonds D J,Li A,et al. Angew. Chem. Int.
[111]  4876—4878
[112]  Asymmetry,1995,6: 2977—2990
[113]  Trost B M,Corte J R. Angew. Chem. Int. Ed. ,1999,38:
[114]  1999,38: 3662—3664
[115]  Allbutt A D,Ayer W A,Brodie H J,et al. Can. J. Microbiol. ,
[116]  1971,17: 1401—1407
[117]  Ayer W A,Lee S P. Can. J. Chem. ,1979,57: 3332—3337
[118]  Trost B M,Dong L,Schroeder G M. J. Am. Chem. Soc. ,
[119]  2005,127: 2844—2845
[120]  Trost B M,Dong L,Schroeder G M. J. Am. Chem. Soc. ,
[121]  2005,127: 10259—10268
[122]  [1 ] Hudlicky T,Price J D. Chem. Rev. ,1989,89: 1467—1486
[123]  [2 ] Trost B M. Chem. Soc. Rev. ,1982,11: 141—170
[124]  [5 ] Aubert C,Buisine O,Malacria M. Chem. Rev. ,2002,102:
[125]  [6 ] Tenaglia A,Heumann A. Angew. Chem. Int. Ed. ,1999,38:
[126]  [7 ] Dounay A B,Overman L E. Chem. Rev. ,2003,103: 2945—
[127]  2963
[128]  [8 ] Montgomery J. Angew. Chem. Int. Ed. ,2004,43: 3890—
[129]  3908
[130]  Trost B M. Science,1991,254: 1471—1477
[131]  Trost B M,Lautens M. J. Am. Chem. Soc. , 1985, 107:
[132]  1781—1783
[133]  Ojima I,Tzamarioudaki M,Li Z,et al. Chem. Rev. ,1996,
[134]  Echavarren A M,Nevado C. Chem. Soc. Rev. ,2004,33:
[135]  431—436
[136]  Bruneau C. Angew. Chem. Int. Ed. ,2005,44: 2328—2334
[137]  Zhang L,Sun J,Kozmin S A. Adv. Synth. Catal. ,2006,348:
[138]  2271—2296
[139]  Fairlamb I J S. Angew. Chem. Int. Ed. ,2004,43: 1048—
[140]  1052

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133