Lanthanide formamidinates as improved catalysts for the Tishchenko reaction

The tris(formamidinato)lanthanum(III) complexes [La(o-TolForm)3(thf)2] [1; o-TolForm = N,N′-bis(o-tolyl)formamidinate], [La(XylForm)3(thf)] [2; XylForm = N,N′-bis(2,6-dimethylphenyl)formamidinate], and [La(EtForm)3] [3, EtForm = N,N′-bis(2,6-diethylphenyl)formamidinate] are a new class of precatalysts for the Tishchenko reaction. Their catalytic activity is a result of their high Lewis acidity and the ease with which the ligand spheres can be interchanged. For the dimerization of benzaldehyde to give benzyl benzoate, which is a benchmark reaction, compound 1 is, to the best of our knowledge, the most active catalyst ever reported. On a preparative scale, the reaction can be performed in the absence of solvent. A range of aromatic, heteroaromatic, and aliphatic aldehydes was rapidly converted into the corresponding esters by using catalysts 1–3.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

[1]  G. Deacon,et al.  Steric modulation of coordination number and reactivity in the synthesis of lanthanoid(III) formamidinates. , 2007, Chemistry.

[2]  A. Barrett,et al.  Heavier alkaline Earth amides as catalysts for the Tischenko reaction. , 2007, Organic letters.

[3]  J. Młynarski Direct Asymmetric Aldol‐Tishchenko Reaction , 2006 .

[4]  J. Frelek,et al.  Chiral ytterbium complex-catalyzed direct asymmetric aldol-Tishchenko reaction: synthesis of anti-1,3-diols. , 2006, Chemistry.

[5]  P. Tuchinda,et al.  Samarium dienolate mediated stereoselective synthesis of anti-1,3-diol monoesters via aldol-Tishchenko reaction , 2006 .

[6]  M. Onaka,et al.  The Tishchenko Reaction: A Classic and Practical Tool for Ester Synthesis , 2006 .

[7]  M. Shibasaki,et al.  Dynamic structural change of the self-assembled lanthanum complex induced by lithium triflate for direct catalytic asymmetric aldol-Tishchenko reaction. , 2005, Chemistry.

[8]  Zhenyu Zhu,et al.  Modification of mesoporous silicate SBA-15 with tris[bis(trimethylsilyl)amido]samarium and its utility in Tishchenko reaction , 2005 .

[9]  T. Katoh,et al.  Tishchenko Reaction Using an Iridium-Ligand Bifunctional Catalyst , 2005 .

[10]  Masakatsu Shibasaki,et al.  Direct catalytic asymmetric aldol-Tishchenko reaction. , 2004, Journal of the American Chemical Society.

[11]  R. Mahrwald The Aldol-Tishchenko Reaction: A Tool in Stereoselective Synthesis , 2003 .

[12]  K. Maruoka,et al.  Isopropoxyaluminum 1,1′-biphenyl-2-oxy-2′-perfluorooctanesulfonamide as a catalyst for Tishchenko reaction , 2003 .

[13]  G. Molander,et al.  Lanthanocene catalysts in selective organic synthesis. , 2002, Chemical reviews.

[14]  V. Nevalainen,et al.  Symmetric esters by Tischtschenko reaction of aldehydes catalyzed by bi- and tridentate catalysts derived from catechol or gallol, trimethylaluminum and isopropanol , 2001 .

[15]  P. Roesky,et al.  Homoleptic lanthanide amides as homogeneous catalysts for alkyne hydroamination and the Tishchenko reaction. , 2001, Chemistry.

[16]  G. Deacon,et al.  Simple syntheses, structural diversity, and Tishchenko reaction catalysis of neutral homoleptic rare earth(II or III) 3,5-di-tert-butylpyrazolates--the structures of. , 2001, Chemistry.

[17]  C. Schneider,et al.  Zr(OtBu)4-catalysed synthesis ofacetone aldol adducts and domino aldol-Tishchenko reactions with diacetonealcohol as enol equivalent , 2001 .

[18]  C. Moïse,et al.  A Combination of Allyltitanation and Tandem Aldol-Tischtschenko Reactions Using Tetraisopropoxytitanium , 2000 .

[19]  O. Blacque,et al.  Study of a tandem aldol–Tischtschenko reaction between chiral enolsilanes and aldehydes catalyzed by titanium(IV) isopropoxide , 2000 .

[20]  S. Kobayashi Lanthanide Triflate-Catalyzed Carbon-Carbon Bond-Forming Reactions in Organic Synthesis , 1999 .

[21]  K. Maruoka,et al.  Catalytic, high-speed tishchenko reaction using (2,7-dimethyl-1,8-biphenylenedioxy)bis(diisopropoxyaluminum) as a powerful bidentate catalyst , 1999 .

[22]  Jim-Min Fang,et al.  Samarium Ion-Promoted Cross-Aldol Reactions and Tandem Aldol/Evans-Tishchenko Reactions. , 1999, The Journal of organic chemistry.

[23]  C. Bolm,et al.  Transition Metals for Organic Synthesis , 1998 .

[24]  P. Roesky,et al.  Homoleptische Lanthanoidamide als Homogenkatalysatoren für die Tischtschenko-Reaktion , 1998 .

[25]  K. Woerpel,et al.  Tandem Aldol−Tishchenko Reactions of Lithium Enolates: A Highly Stereoselective Method for Diol and Triol Synthesis , 1997 .

[26]  B. Costisella,et al.  Titanium-Mediated Aldol-Tishchenko Reaction: A Stereoselective Synthesis of Differentiated anti 1,3-Diol Monoesters , 1996 .

[27]  T. Sakakura,et al.  Lanthanoid-catalysed Tishchenko reaction of mono- or di-aldehydes , 1996 .

[28]  G. Molander,et al.  Sequencing Reactions with Samarium(II) Iodide. , 1996, Chemical reviews.

[29]  T. Ikariya,et al.  Amino alcohol effects on the ruthenium(II)-catalysed asymmetric transfer hydrogenation of ketones in propan-2-ol , 1996 .

[30]  I. Hachiya,et al.  Repeated Use of the Catalyst in Ln(OTf)3-Catalyzed Aldol and Allylation Reactions , 1994 .

[31]  Shuj Kobayashi,et al.  Lanthanide triflates as water-tolerant Lewis acids. Activation of commercial formaldehyde solution and use in the aldol reaction of silyl enol ethers with aldehydes in aqueous media , 1994 .

[32]  H. Ishitani,et al.  Lanthanide (III)-catalyzed enantioselective Diels-Alder reactions. Stereoselective synthesis of both enantiomers by using a single chiral source and a choice of achiral ligands , 1994 .

[33]  S. Mitamura,et al.  Scandium Trifluoromethanesulfonate. A Novel Catalyst for Friedel- Crafts Acylation. , 1994 .

[34]  S. Kobayashi Rare Earth Metal Trifluoromethanesulfonates as Water-Tolerant Lewis Acid Catalysts in Organic Synthesis , 1994 .

[35]  Y. Ishii,et al.  Selective dimerization of aldehydes to esters catalyzed by zirconocene and hafnocene complexes , 1993 .

[36]  T. Ohishi,et al.  Dimerization of aldehydes to carboxylic esters catalyzed by K2[Fe(CO)4]–crown ether system , 1993 .

[37]  I. Hachiya,et al.  Scandium trifluoromethanesulfonate (Sc(OTf)3). A novel reusable catalyst in the Diels-Alder reaction , 1993 .

[38]  H. Ohno,et al.  Lanthanoid(III) Alkoxides as Novel Catalysts for a Rapid Transhydrocyanation from Acetone Cyanohydrin to Aldehydes and Ketones , 1993 .

[39]  S. Kobayashi,et al.  Lanthanide trifluoromethanesulfonates as reusable catalysts: catalytic Friedel-Crafts acylation , 1993 .

[40]  I. Hachiya,et al.  Lanthanide trifluoromethanesulfonates as reusable catalysts. Michael and Diels-Alder reactions , 1992 .

[41]  G. Molander Application of lanthanide reagents in organic synthesis , 1992 .

[42]  H. Alper,et al.  Homogeneous metal-catalyzed sequential Rosenmund-Tishchenko reactions , 1991 .

[43]  Davidr . Evans,et al.  Samarium-catalyzed intramolecular Tishchenko reduction of .beta.-hydroxy ketones. A stereoselective approach to the synthesis of differentiated anti 1,3-diol monoesters , 1990 .

[44]  R. Bergman,et al.  Synthesis and reactions of nickel and palladium carbon-bound enolate complexes , 1990 .

[45]  M. Ishar,et al.  Regio- and stereo-selectivity in uncatalysed and catalysed Diels–Alder reactions of allenic esters with furan and 2-methylfuran , 1990 .

[46]  T. Okano,et al.  Meerwein-Ponndorf-Verley Reduction of Ketones and Aldehydes Catalyzed by Lanthanide Tri-2-propoxides , 1987 .

[47]  J. Collin,et al.  New preparations of lanthanide alkoxides and their catalytical activity in Meerwein-Ponndorf-Verley-Oppenauer reactions , 1984 .

[48]  S. Danishefsky,et al.  Total synthesis of vineomycin B2 aglycon , 1984 .

[49]  G. Villacorta,et al.  Lithium tungsten dioxide promoted Claisen-Tishchenko condensation of aromatic and aliphatic aldehydes , 1983 .

[50]  Y. Koshiro,et al.  Selective Dimerization of Aldehydes to Esters Catalyzed by Hydridoruthenium Complexes , 1982 .

[51]  K. Chiba,et al.  THE SYNTHESIS OF BENZOLACTONES BY PALLADIUM-CATALYZED CARBONYLATION , 1979 .

[52]  G. Fouquet,et al.  Über die Tischtschenko‐Reaktion von Aldolen , 1979 .

[53]  Yoshihisa Watanabe,et al.  The Reaction of Disodium Tetracarbonylferrate(–II) with Aldehydes , 1976 .

[54]  P. Stapp Boric acid catalyzed Tishchenko reactions , 1973 .

[55]  E. G. Hawkins,et al.  Reaction of 1 : 2 : 3 : 6-tetrahydrobenzaldehyde with alkali , 1955 .

[56]  A. Day,et al.  A Study of the Mixed Tischtschenko Reaction , 1952 .

[57]  F. Nord,et al.  Essential Steps in the Catalytic Condensation of Carbonyl Compounds. III. The Action of Metallic Alkoxides1 , 1947 .

[58]  L. Claisen Ueber die Einwirkung von Natriumalkylaten auf Benzaldehyd , 1887 .