OALib Journal期刊
ISSN: 2333-9721
费用:99美元
|
|
|
铑-ImiFerroPhos配合物对β-取代-α,β-不饱和磷酸酯的不对称氢化
DOI: 10.1016/S1872-2067(12)60742-6, PP. 227-231
Keywords: β-取代-α,β-不饱和磷酸酯,不对称催化氢化,ImiFerroPhos配体,铑(Ⅱ)配合物,手性β-取代烷基磷酸酯
Abstract:
?将手性二茂铁双膦配体ImiFerroPhos应用到β-取代-α,β-不饱和磷酸酯的不对称氢化反应中,在温和的反应条件下,以高收率及较高对映选择性合成了一系列β-取代的手性磷酸酯,最高获得了92%的ee值.
References
[1] | Bellucci C, Gualtieri F, Scapecchi S, Teodori E, Budriesi R, Chiarini A. Farmaco, 1989, 44: 1167
|
[2] | Kafarski P, Lejczak B. Phosphorus Sulfur Silicon Relat Elem, 1991, 63: 193
|
[3] | Jung K W, Janda K D, Sanfilippo P J, Wachter M. Bioorg Med Chem Lett, 1996, 6: 2281
|
[4] | Lo C H L, Wentworth P Jr, Jung K W, Yoon J, Ashley J A, Janda K D. J Am Chem Soc, 1997, 119: 10251
|
[5] | Datta A, Wentworth P Jr, Shaw J P, Simeonov A, Janda K D. J Am Chem Soc, 1999, 121: 10461
|
[6] | Kolodiazhnyi O I. Tetrahedron: Asymmetry, 2005, 16: 3295
|
[7] | Kelly S E. In: Trost B M, Fleming I Eds. Comprehensive Organic Synthesis. Vol. 1. Oxford: Pergamon, 1991. 761
|
[8] | Omelanzcuk J, Sopchik A E, Lee S G, Akutagawa K, Cairns S M, Bentrude W G. J Am Chem Soc, 1988, 110: 6908
|
[9] | Cairns S M, Bentrude W G. Tetrahedron Lett, 1989, 30: 1025
|
[10] | Denmark S E, Chen C T. J Am Chem Soc, 1995, 117: 11879
|
[11] | Kranz M, Denmark S E. J Org Chem, 1995, 60: 5867
|
[12] | Noyori R. Asymmetric Catalysis in Organic Synthesis. New York: Wiley, 1994
|
[13] | Jacobsen E N, Pfaltz A, Yamamoto H. Comprehensive Asymmetric Catalysis. Vol. 1-3. Berlin: Springer, 1999
|
[14] | de Vries J G, Elsevier C J. The Handbook of Homogeneous Hydrogenation. Vol. 1-3. Weinheim: Wiley-VCH, 2007
|
[15] | Sun H J, Pan Y J, Li S H, Zhang Y X, Dong Y Y, Liu S C, Liu Z Y. J Energy Chem, 2013, 22: 710
|
[16] | Hilderbrand R L. The Role of Phosphonates in Living Systems. Boca Raton: CRC Press, 1983
|
[17] | Kafarski P, Lejczak B. Curr Med Chem: Anti-Cancer Agents, 2001, 1: 301
|
[18] | Savignac P, Iorga B. Morden Phosphonate Chemistry. Boca Raton: CRC Press, 2003
|
[19] | Bennani Y L, Hanessian S. Tetrahedron, 1996, 52: 13837
|
[20] | Bhanthumnavin W, Arif A, Bentrude W G. J Org Chem, 1998, 63: 7753
|
[21] | Goulioukina N S, Dolgina T M, Beletskaya I P, Henry J C, Lavergne D, Ratovelomanana-Vidal V, Genet J P. Tetrahedron: Asymmetry, 2001, 12: 319
|
[22] | Goulioukina N S, Dolgina T M, Bondarenko G N, Beletskaya I P, Ilyin M M, Davankov V A, Pfaltz A. Tetrahedron: Asymmetry, 2003, 14: 1397
|
[23] | Hayashi T, Senda T, Takaya Y, Ogasawara M. J Am Chem Soc, 1999, 121: 11591
|
[24] | Duan Z C, Hu X P, Wang D Y, Yu S B, Zheng Z. Tetrahedron Lett, 2009, 50: 6720
|
[25] | Konno T, Shimizu K, Ogata K, Fukuzawa S-i. J Org Chem, 2012, 77: 3318
|
[26] | Ojima I. Catalytic Asymmetric Synthesis. 2nd Ed. New York: Wiley-VCH, 2000
|
[27] | Tang W J, Zhang X M. Chem Rev, 2003, 103: 3029
|
[28] | Minnaard A J, Feringa B L, Lefort L, de Vries J G. Acc Chem Res, 2007, 40: 1267
|
[29] | Chen P R, Chew L M, Kostka A, Xie K P, Muhler M, Xia W. J Energy Chem, 2013, 22: 312
|
[30] | Duan Z C, Hu X P, Wang D Y, Huang J D, Yu S B, Deng J, Zheng Z. Adv Synth Catal, 2008, 350: 1979
|
[31] | Duan Z C, Wang L Z, Song X J, Hu X P, Zheng Z. Tetrahedron: Asymmetry, 2012, 23: 508
|
[32] | Duan Z C, Hu X P, Zhang C, Wang D Y, Yu S B, Zheng Z. J Org Chem, 2009, 74: 9191
|
[33] | Luo L B, Wang D Y, Zhou X M, Zheng Z, Hu X P. Tetrahedron: Asymmetry, 2011, 22: 2117
|
[34] | Wang D Y, Hu X P, Hou C J, Deng J, Yu S B, Duan Z C, Huang J D, Zheng Z. Org Lett, 2009, 11: 3226
|
Full-Text
|
|
Contact Us
service@oalib.com QQ:3279437679 
WhatsApp +8615387084133
|
|