Chemoselective hydrogenation method catalyzed by Pd/C using diphenylsulfide as a reasonable catalyst poison
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Y. Monguchi | H. Sajiki | T. Maegawa | Akinori Mori | Tomoteru Mizusaki | Eri Ohashi | Yumi Miyakawa | T. Haga
[1] H. Sajiki,et al. Pd/C-catalyzed chemoselective hydrogenation in the presence of diphenylsulfide. , 2006, Organic letters.
[2] X. Bao,et al. Ag/SiO2: a novel catalyst with high activity and selectivity for hydrogenation of chloronitrobenzenes. , 2005, Chemical communications.
[3] H. Sajiki,et al. Highly chemoselective hydrogenation method using novel finely dispersed palladium catalyst on silk-fibroin: its preparation and activity , 2005 .
[4] H. Sajiki,et al. Solvent-modulated Pd/C-catalyzed deprotection of silyl ethers and chemoselective hydrogenation , 2004 .
[5] R. V. Chaudhari,et al. Chemoselective hydrogenation of substituted nitroaromatics using novel water-soluble iron complex catalysts. , 2004, The Journal of organic chemistry.
[6] H. Sajiki,et al. Markedly chemoselective hydrogenation with retention of benzyl ester and N-Cbz functions using a heterogeneous Pd-fibroin catalyst , 2003 .
[7] T. Kan,et al. Stereocontrolled total synthesis of (-)-ephedradine A (orantine). , 2003, Journal of the American Chemical Society.
[8] H. Sajiki,et al. Pd/C-catalyzed chemoselective hydrogenation in the presence of a phenolic MPM protective group using pyridine as a catalyst poison. , 2003, Chemical & pharmaceutical bulletin.
[9] H. Sajiki,et al. A remarkable solvent effect toward the Pd/C-catalyzed cleavage of silyl ethers. , 2003, Chemical communications.
[10] H. Sajiki,et al. Preparation of silk fibroin-supported Pd(0) catalyst for chemoselective hydrogenation: reduction of palladium(II) acetate by methanol on the protein , 2003 .
[11] H. Sajiki,et al. Chemoselective control of hydrogenation among aromatic carbonyl and benzyl alcohol derivatives using Pd/C(en) catalyst , 2001 .
[12] H. Sajiki,et al. Undesirable deprotection of O-TBDMS groups by Pd/D-catalyzed hydrogenation and chemoselective hydrogenation Using a Pd/C(en) catalyst. , 2001 .
[13] H. Sajiki,et al. Formation of Pd/C-ethylenediamine Complexes [Pd/C (en)] and It's Application to Selective Hydrogenations , 2001 .
[14] S. Nishimura. Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis , 2001 .
[15] H. Sajiki. [Development of a novel type of Pd/C-catalyzed chemoselective hydrogenation using a nitrogen catalyst poison]. , 2000, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.
[16] H. Sajiki,et al. Pd/C(en)-Catalyzed Chemoselective Hydrogenation with Retention of the N-Cbz Protective Group and its Scope and Limitations , 2000 .
[17] H. Sajiki,et al. The undesirable lability of tert-butyldimethylsilyl ethers under Pd/C-catalyzed hydrogenation conditions and solution of the problem by using a Pd/C(en) catalyst , 2000 .
[18] Hirota,et al. Highly chemoselective hydrogenation with retention of the epoxide function using a heterogeneous Pd/C-ethylenediamine catalyst and THF , 2000, Chemistry.
[19] Y. Cho,et al. Chemoselective reduction of nitroaromatics to anilines using decaborane in methanol , 2000 .
[20] M. Reetz,et al. Chemoselective Reduction of Halo-Nitro Aromatic Compounds by β-Cyclodextrin-Modified Transition Metal Catalysts in a Biphasic System , 1999 .
[21] G. Zappia,et al. Selective Catalytic Hydrogenation of γ-Amino α,β-Unsaturated Esters in the Presence of Hydrogenable Protecting Groups , 1999 .
[22] H. Sajiki,et al. Pd/C(en)-catalyzed regioselective hydrogenolysis of terminal epoxides to secondary alcohols , 1999 .
[23] Hirota,et al. Easy and Partial Hydrogenation of Aromatic Carbonyls to Benzyl Alcohols Using Pd/C(en)-Catalyst. , 1999 .
[24] H. Sajiki,et al. A novel type of hydrogenation using a catalyst poison: Chemoselective inhibition of the hydrogenolysis for O-benzyl protective group by the addition of a nitrogen-containing base , 1998 .
[25] H. Sajiki,et al. The Formation of a Novel Pd/C-Ethylenediamine Complex Catalyst : Chemoselective Hydrogenation without Deprotection of the O-Benzyl and N-Cbz Groups. , 1998 .
[26] H. Sajiki,et al. Suppression effect of the Pd/C-catalyzed hydrogenolysis of a phenolic benzyl protective group by the addition of nitrogen-containing bases , 1998 .
[27] H. Sajiki,et al. Chemoselective Inhibition of the Hydrogenolysis of the MPM Protective Group for Phenolic Hydroxy Functions Using a Pd/C-Pyridine Catalyst. , 1997 .
[28] H. Sajiki. Selective Inhibition of Benzyl Ether Hydrogenolysis with Pd/C Due to the Presence of Ammonia, Pyridine or Ammonium Acetate. , 1995 .
[29] H. Sakurai,et al. Hypervalent Iodine-Induced Nucleophilic Substitution of para-Substituted Phenol Ethers. Generation of Cation Radicals as Reactive Intermediates , 1994 .
[30] R. Larock. Comprehensive Organic Transformations , 1989 .
[31] M. Hudlický. Reductions in organic chemistry , 1984 .
[32] P. Hodge,et al. Protective groups in organic synthesis , 1981 .
[33] H. Greenfield,et al. Platinum Metal Sulfides as Heterogeneous Hydrogenation Catalysts , 1965 .
[34] H. Oelschläger. Über die Spaltung der Kohlenstoff‐Sauerstoff‐Bindung bei der Hydrierung von N‐allylierten N‐[γ‐(4‐Phenoxymethylphenyl)‐propyl]‐aminen , 1960 .
[35] K. Rosenmund,et al. Über Katalysator‐Beeinflussung und spezifisch wirkende Katalysatoren , 1921 .
[36] K. Rosenmund. Über eine neue Methode zur Darstellung von Aldehyden. 1. Mitteilung , 1918 .