OALib Journal期刊
ISSN: 2333-9721
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银催化羧化偶联反应及钌催化交叉复分解反应串联合成官能团炔酸酯
DOI: 10.1016/S1872-2067(12)60527-0, PP. 1179-1186
Keywords: 二氧化碳,羧化偶联反应,银催化剂,交叉复分解反应,Grubbs-Hoveyda催化剂,均相催化
Abstract:
?通过将Ag催化的羧化偶联反应与Ru催化的交叉复分解反应串联,用端炔、二氧化碳、端烯基取代的溴代物和甲基丙烯酸甲酯高效高产率地合成了一系列官能团化的炔酸酯.
References
[1] | Donohoe T J, Bower J F, Chan L K M. Org Biomol Chem, 2012, 10: 1322
|
[2] | Gessler S, Randl S, Blechert S. Tetrahedron Lett, 2000, 41: 9973
|
[3] | Chatterjee A K, Choi T L, Sanders D P, Grubbs R H. J Am Chem Soc, 2003, 125: 11360
|
[4] | Ornelas C, Mery D, Cloutet E, Aranzaes J R, Astruc D. J Am Chem Soc, 2008, 130: 1495
|
[5] | McDougal N T, Virgil S C, Stoltz B M. Synlett, 2010, 1712
|
[6] | Voigtritter K, Ghorai S, Lipshutz B H. J Org Chem, 2011, 76: 4697
|
[7] | Miao X, Malacea R, Fischmeister C, Bruneau C, Dixneuf P H. Green Chem, 2011, 13: 2911
|
[8] | Ma S, Lu X. J Org Chem, 1993, 58: 1245
|
[9] | Rayabarapu D K, Tunge J A. J Am Chem Soc, 2005, 127: 13510
|
[10] | Yin G, Liu G. Angew Chem, Int Ed 2008, 47: 5442
|
[11] | Luo T, Schreiber S L. J Am Chem Soc, 2009, 131: 5667
|
[12] | Sakakura T, Choi J C, Yasuda H. Chem Rev, 2007, 107: 2365
|
[13] | Riduan S N, Zhang Y G. Dalton Trans, 2010, 39: 3347
|
[14] | Huang K, Sun C L, Shi Z J. Chem Soc Rev, 2011, 40: 2435
|
[15] | Cokoja M, Bruckmeier C, Rieger B, Herrmann W A, Kuhn F. E. Angew Chem, Int Ed, 2011, 50: 8510
|
[16] | Lü X B, Darensbourg D J. Chem Soc Rev, 2012, 41: 1462
|
[17] | Zhang W Z, Lü X B. Chin J Catal (张文珍, 吕小兵. 催化学报), 2012, 33: 745
|
[18] | Tsuji Y, Fujihara T. Chem Commun, 2012, 48: 9956
|
[19] | Shi M, Nicholas K M. J Am Chem Soc, 1997, 119: 5057
|
[20] | Yeung C S, Dong V M. J Am Chem Soc, 2008, 130: 7826
|
[21] | Ukai K, Aoki M, Takaya J, Iwasawa N. J Am Chem Soc, 2006, 128: 8706
|
[22] | Ohishi T, Nishiura M, Hou Z M. Angew Chem, Int Ed, 2008, 47: 5792
|
[23] | Zhang X, Zhang W Z, Shi L L, Guo C X, Zhang L L, Lu X B. Chem Commun, 2012, 48: 6292
|
[24] | Boogaerts I I F, Nolan S P. J Am Chem Soc, 2010, 132: 8858
|
[25] | Zhang L, Cheng J, Ohishi T, Hou Z. Angew Chem, Int Ed, 2010, 49: 8670
|
[26] | Mizuno H, Takaya J, Iwasawa N. J Am Chem Soc, 2011, 133: 1251
|
[27] | Correa A, Martin R. J Am Chem Soc, 2009, 131: 15974
|
[28] | Fujihara T, Nogi K, Xu T, Terao J, Tsuji Y. J Am Chem Soc, 2012, 134: 9106
|
[29] | Takaya J, Iwasawa N. J Am Chem Soc, 2008, 130: 15254
|
[30] | Williams C M, Johnson J B, Rovis T. J Am Chem Soc, 2008, 130: 14936
|
[31] | Fujihara T, Xu T H, Semba K, Terao J, Tsuji Y. Angew Chem, Int Ed, 2011, 50: 523
|
[32] | Li S H, Yuan W M, Ma S M. Angew Chem, Int Ed, 2011, 50: 2578
|
[33] | Zhang L, Cheng J H, Carry B, Hou Z M. J Am Chem Soc, 2012, 134: 14314
|
[34] | Manjolinho F, Arndt M, Goossen K, Goossen L J. ACS Catal, 2012, 2: 2014
|
[35] | Fukue Y, Oi S, Inoue Y. J Chem Soc Chem Commun, 1994, 2091
|
[36] | Eghbali N, Eddy J, Anastas P T. J Org Chem, 2008, 73: 6932
|
[37] | Goosen L J, Rodriguez N, Manjolinho F, Lange P P. Adv Synth Catal, 2010, 352: 2913
|
[38] | Yu D Y, Zhang Y G. Proc Natl Acad Sci USA, 2010, 107: 20184
|
[39] | Zhang W Z, Li W J, Zhang X, Zhou H, Lu X B. Org Lett, 2010, 12: 4748
|
[40] | Yu D Y, Zhang Y G. Green Chem, 2011, 13: 1275
|
[41] | Zhang X, Zhang W Z, Ren X, Zhang L L, Lu X B. Org Lett, 2011, 13: 2402
|
[42] | Arndt M, Risto E, Krause T, Goossen L J. ChemCatChem, 2012, 4: 484
|
[43] | Yu D, Tan M X, Zhang Y. Adv Synth Catal, 2012, 354: 969
|
[44] | Inamoto K, Asano N, Kobayashi K, Yonemoto M, Kondo Y. Org Biomol Chem, 2012, 10: 1514
|
[45] | Zhang X, Zhang W Z, Shi L L, Zhu C, Jiang J L, Lu X B. Tetrahedron, 2012, 68: 9085
|
[46] | Chauvin Y. Angew Chem, Int Ed, 2006, 45: 3740
|
[47] | Schrock R R. Angew Chem, Int Ed, 2006, 45: 3748
|
[48] | Grubbs R H. Angew Chem, Int Ed, 2006, 45: 3760
|
[49] | Grubbs R H. Tetrahedron, 2004, 60: 7117
|
[50] | Astruc D. New J Chem, 2005, 29: 42
|
[51] | Nicolaou K C, Bulger P G, Sarlah D. Angew Chem, Int Ed, 2005, 44: 4490
|
[52] | Schrodi Y, Pederson R L. Aldrichim Acta, 2007, 40(2): 45
|
[53] | Connon S J, Blechert S. Angew Chem, Int Ed, 2003, 42: 1900
|
[54] | Prunet J. Curr Top Med Chem, 2005, 5: 1559
|
[55] | Tsujihara T, Takenaka K, Onitsuka K, Hatanaka M, Sasai H. J Am Chem Soc, 2009, 131: 3452
|
[56] | Zhang L L, Zhang W Z, Ren X, Tan X Y, Lü X B. Tetrahedron Lett, 2012, 53: 3389
|
[57] | Scholl M, Ding S, Lee C W, Grubbs R H. Org Lett, 1999, 1: 953
|
[58] | Trnka T M, Morgan J P, Sanford M S, Wilhelm T E, Scholl M, Choi T L, Ding S, Day M W, Grubbs R H. J Am Chem Soc, 2003, 125: 2546
|
[59] | Garber S B, Kingsbury J S, Gray B L, Hoveyda A H. J Am Chem Soc, 2000, 122: 8168
|
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