Subscribe to RSS
DOI: 10.1055/s-0028-1088001
Catalytic Transformations of Benzylic Carboxylates and Carbonates
Publication History
Publication Date:
06 March 2009 (online)
Abstract
Benzylic carboxylates and carbonates react with various molecules in the presence of homogeneous palladium or cobalt catalysts. The catalytic transformations occur at the benzylic carbons of the substrates, affording benzylic substitution products. This review surveys the catalytic reactions using benzylic carboxylates and carbonates as substrates. Furthermore, the related studies on (η³-benzyl)metal complexes are summarized in order to facilitate the understanding and consideration of the catalytic substitution.
1 Introduction
2 Chemistry of the (η³-Benzyl)metal Complex
2.1 Structure of the (η³-Benzyl)metal Complex
2.2 Reactivity of the (η³-Benzyl)metal Complex
3 Catalytic Transformations of Benzylic Esters
3.1 Nucleophilic Substitution
3.2 Cross-Coupling with Organometallic Compounds
3.3 Miscellaneous Reactions
4 Concluding Remarks
Key words
homogeneous catalysis - palladium - benzylation - cross-coupling - benzyl complexes
- 1
Handbook
of Organopalladium Chemistry for Organic Synthesis
Negishi E.-i.de Meijere A. John Wiley & Sons; Hoboken: 2002. - 2
Tsuji J. Palladium Reagents and Catalysts John Wiley & Sons; Chichester: 2004. - 3
Trost BM.Crawley ML. Chem. Rev. 2003, 103: 2921 - 4
Nicolaou KC.Bulger PG.Sarlah D. Angew. Chem. Int. Ed. 2005, 44: 4442 - 5
Hata G.Takahashi K.Miyake A. J. Chem. Soc., Chem. Commun. 1970, 1392 - 6
Atkins KE.Walker WE.Manyik RM. Tetrahedron Lett. 1970, 11: 3821 - 7
Tsuji J. In Palladium Reagents and Catalysts John Wiley & Sons; Chichester: 2004. p.431 - 8
Guibé F. Tetrahedron 1998, 54: 2967 - 9
Trost BM. Acc. Chem. Res. 1980, 13: 385 - 10
Lin Y.-S.Yamamoto A. In Activation of Unreactive Bonds and Organic SynthesisMurai S. Springer; Berlin: 1999. p.161 - 11
Legros J.-Y.Fiaud J.-C. Tetrahedron Lett. 1992, 33: 2509 - 12
Kuwano R.Kondo Y.Matsuyama Y. J. Am. Chem. Soc. 2003, 125: 12104 - 13
Liégault B.Renaud J.-L.Bruneau C. Chem. Soc. Rev. 2008, 37: 290 - 14
King RB.Fronzaglia A. J. Am. Chem. Soc. 1966, 88: 709 - 15
Cotton FA.LaPrade MD. J. Am. Chem. Soc. 1968, 90: 5418 - 16
Faller JW.Chodosh DF.Katahira D. J. Organomet. Chem. 1980, 187: 227 - 17
Chen J.Lei G.Xu W.Jin X.Shao M.Tang Y. J. Organomet. Chem. 1985, 286: 55 - 18
Chen J.Lei G.Xu W.Pan Z.Zhang S.Zhang Z.Jin X.Shao M.Tang Y. Organometallics 1987, 6: 2461 - 19
Bleeke JR.Burch RR.Coulman CL.Schardt BC. Inorg. Chem. 1981, 20: 1316 - 20
Stühler H.-O.Pickardt J. Z. Naturforsch., B 1981, 36: 315 - 21
Burch RR.Muetterties EL.Day VW. Organometallics 1982, 1: 188 - 22
Chappell SD.Cole-Hamilton DJ.Galas AMR.Hursthouse MB.Walker NPC. Polyhedron 1985, 4: 121 - 23
Fryzuk MD.McConville DH.Rettig SJ. J. Organomet. Chem. 1993, 445: 245 - 24
Carmona E.Marin JM.Paneque M.Poveda ML. Organometallics 1987, 6: 1757 - 25
Ascenso JR.Carrondo MAAFdCT.Dias AR.Gomes PT.Fátima M.Piedade M.Romao CC.Revillon A.Tkatchenko I. Polyhedron 1989, 8: 2449 - 26
Crascall LE.Litster SA.Redhouse AD.Spencer JL. J. Organomet. Chem. 1990, 394: C35 - 27
Sonoda A.Bailey PM.Maitlis PM. J. Chem. Soc., Dalton Trans. 1979, 346 - 28
Johns AM.Utsunomiya M.Incarvito CD.Hartwig JF. J. Am. Chem. Soc. 2006, 128: 1828 - 29
Nettekoven U.Hartwig JF. J. Am. Chem. Soc. 2002, 124: 1166 - 30
Gatti G.López JA.Mealli C.Musco A. J. Organomet. Chem. 1994, 483: 77 - 31
Rix FC.Brookhart M.White PS. J. Am. Chem. Soc. 1996, 118: 2436 - 32
Crascall LE.Spencer JL. J. Chem. Soc., Dalton Trans. 1992, 3445 - 33
Su SCH.Wojcicki A. Organometallics 1983, 2: 1296 - 34
Roberts JS.Klabunde KJ. J. Am. Chem. Soc. 1977, 99: 2509 - 35
Johns AM.Tye JW.Hartwig JF. J. Am. Chem. Soc. 2006, 128: 16010 - 36
Legros J.-Y.Toffano M.Fiaud J.-C. Tetrahedron 1995, 51: 3235 - 37
Legros J.-Y.Primault G.Toffano M.Rivière M.-A.Fiaud J.-C. Org. Lett. 2000, 2: 433 - 38
Toffano M.Legros J.-Y.Fiaud J.-C. Tetrahedron Lett. 1997, 38: 77 - 39
Boutros A.Legros J.-Y.Fiaud J.-C. Tetrahedron Lett. 1999, 40: 7297 - 40
Boutros A.Legros J.-Y.Fiaud J.-C. Tetrahedron 2000, 56: 2239 - 41
Lau KSY.Wong PK.Stille JK. J. Am. Chem. Soc. 1976, 98: 5832 - 42
Legros J.-Y.Toffano M.Fiaud J.-C. Tetrahedron: Asymmetry 1995, 6: 1899 - 43
Assié M.Legros J.-Y.Fiaud J.-C. Tetrahedron: Asymmetry 2005, 16: 1183 - 44
Kuwano R.Kondo Y. Org. Lett. 2004, 6: 3545 - 45
Kuwano R.Kusano H. Org. Lett. 2008, 10: 1979 - 46
Kuwano R.Kondo Y.Shirahama T. Org. Lett. 2005, 7: 2973 - 47
Kuwano R.Kusano H. Chem. Lett. 2007, 36: 528 - 48
Yokogi M.Kuwano R. Tetrahedron Lett. 2007, 48: 6109 - 49
Kuwano R.Yokogi M. Org. Lett. 2005, 7: 945 - 50
Kuwano R.Yu J.-Y. Heterocycles 2007, 74: 233 - 51
Kuwano R.Yokogi M. Chem. Commun. 2005, 5899 - 52
McLaughlin M. Org. Lett. 2005, 7: 4875 - 53
Yu J.-Y.Kuwano R. Org. Lett. 2008, 10: 973 - 54
Molander GA.Elia MD. J. Org. Chem. 2006, 71: 9198 - 55
Nakao Y.Ebata S.Chen J.Imanaka H.Hiyama T. Chem. Lett. 2007, 36: 606 - 56
Ohsumi M.Kuwano R. Chem. Lett. 2008, 37: 796 - 57
Lindsey CC.O’Boyle BM.Mercede SJ.Pettus TRR. Tetrahedron Lett. 2004, 45: 867 - 58
Baird JM.Kern JR.Lee GR.Morgans DJ.Sparacino ML. J. Org. Chem. 1991, 56: 1928 - 59
Chatani N.Sano T.Ohe K.Kawasaki Y.Murai S. J. Org. Chem. 1990, 55: 5923 - 60
Narahashi H.Yamamoto A.Shimizu I. Chem. Lett. 2004, 33: 348 - 61
Narahashi H.Shimizu I.Yamamoto A. J. Organomet. Chem. 2008, 693: 283 - 62
Nagayama K.Shimizu I.Yamamoto A. Bull. Chem. Soc. Jpn. 1999, 72: 799 - 63
Kuwano R.Shige T. J. Am. Chem. Soc. 2007, 129: 3802