Hydrogenation of Esters

作者: Lionel A. Saudan

DOI: 10.1002/9781118354520.CH02

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摘要:

参考文章(71)
Anthony A. Birkbeck, Challenges in the Synthesis of Natural and Non‐Natural Volatiles John Wiley & Sons, Ltd. pp. 173- 202 ,(2010) , 10.1002/9780470669532.CH7
Herman T. Teunissen, Cornelis J. Elsevier, Ruthenium catalysed hydrogenation of dimethyl oxalate to ethylene glycol Chemical Communications. pp. 667- 668 ,(1997) , 10.1039/A700862G
Kamaluddin Abdur-Rashid, Rongwei Guo, Alan?J. Lough, Robert?H. Morris, Datong Song, Synthesis of Ruthenium Hydride Complexes Containing beta-Aminophosphine Ligands Derived from Amino Acids and their use in the H2-Hydrogenation of Ketones and Imines Advanced Synthesis & Catalysis. ,vol. 347, pp. 571- 579 ,(2005) , 10.1002/ADSC.200404274
Pieter D. de Koning, Mark Jackson, Ian C. Lennon, Use of Achiral (Diphosphine)RuCl2(Diamine) Precatalysts as a Practical Alternative to Sodium Borohydride for Ketone Reduction Organic Process Research & Development. ,vol. 10, pp. 1054- 1058 ,(2006) , 10.1021/OP060063N
Takeshi Ohkuma, Masatoshi Koizumi, Kilian Muñiz, Gerhard Hilt, Chizuko Kabuto, Ryoji Noyori, trans-RuH(η1-BH4)(binap)(1,2-diamine): A Catalyst for Asymmetric Hydrogenation of Simple Ketones under Base-Free Conditions Journal of the American Chemical Society. ,vol. 124, pp. 6508- 6509 ,(2002) , 10.1021/JA026136+
Brian A. Keay, Synthesis of multi-substituted furan rings: the role of silicon Chemical Society Reviews. ,vol. 28, pp. 209- 215 ,(1999) , 10.1039/A809439J
Tse-Lok Ho, Kwang-Yuan Lee, A new synthesis of (−)-furodysin Tetrahedron Letters. ,vol. 36, pp. 947- 948 ,(1995) , 10.1016/0040-4039(94)02464-M
Frédéric Naud, Felix Spindler, Carsten J. Rueggeberg, Andreas T. Schmidt, Hans-Ulrich Blaser, Enantioselective Ketone Hydrogenation: From R&D to Pilot Scale with Industrially Viable Ru/Phosphine−Oxazoline Complexes Organic Process Research & Development. ,vol. 11, pp. 519- 523 ,(2007) , 10.1021/OP0601619
Herman T. Teunissen, Homogeneous ruthenium catalyzed hydrogenation of esters to alcohols Chemical Communications. pp. 1367- 1368 ,(1998) , 10.1039/A801807C