Subscribe to RSS
DOI: 10.1055/s-2004-837190
Preparation of Magnesium Enolates of α-Keto Esters and Synthetic Applications
Publication History
Publication Date:
17 December 2004 (online)
Abstract
The reaction between α-chloroglycidic esters 1 and magnesium iodide in the presence of an excess of active magnesium led to magnesium α-ketoester enolates 3. Some synthetic applications of these new reagents are reported.
Key words
pyruvic ester - α-keto esters - magnesium enolate - α-chloroglycidic esters - β-iodo-α-ketoesters
- 2
Stryer L. La Biochimie 2nd ed.: Flammarion Médecine Sciences; Paris: 1985. -
3a
Unger FM. Adv. Carbohydr. Chem. Biochem. 1981, 38: 323 -
3b
Levi DH.Racker EJ. J. Biol. Chem. 1959, 234: 2532 -
4a
Chapter D.Nadano D.Iwasaki M.Endo S.Kitajima K.Inoue Y. J. Biol. Chem. 1986, 261: 11550 -
4b
Sialic Acids, Chemistry Metabolism and Function
Schauer R. Springer-Verlag; New York: 1982. -
5a
Haslam E. In Shikimic Acid Metabolism and Metabolites Wiley; New York: 1993. -
5b DeLeo A. B., Sprinson D. B.; Biochem. Biophys. Res. Commun.; 1968, 32: 873
-
6a
Barton DHR.De Almeida MV.Liu W.Shunada T.Jaszberenyi JC.Dos Santos HF.LeHyaric M. Tetrahedron 2001, 57: 8767 -
6b
Sugisaki CH.Ruland Y.Le Clezio I.Baltas M. Synlett 2001, 1905 -
6c
Warwel M.Fessner WD. Synlett 2000, 865 -
6d
Tsukamoto H.Takahashi T. Tetrahedron Lett. 1997, 6415 -
6e
Barton DHR.Liu W. Tetrahedron Lett. 1997, 367 -
6f
Choi SK.Lee S.Whitesides GM. J. Org. Chem. 1996, 61: 8739 -
6g
Jaszberenyi JC.Liu W.Shinada T. Tetrahedron 1996, 52: 2717 -
6h
Chan TH.Li CJ. J. Org. Chem. 1995, 60: 4228 -
6i
Dondoni A.Marra A.Merino P. J. Am. Chem. Soc. 1994, 116: 3324 -
6j
Kovacs L. Recl. Trav. Chim. Pays-Bas 1993, 112: 471 ; and references cited therein -
6k
Enders D.Dyker H.Raabe G. Angew. Chem., Int. Ed. Engl. 1993, 32: 421 -
6l
Enders D.Dyker H.Raabe G. Angew. Chem., Int. Ed. Engl. 1992, 31: 618 -
6m
Enders D.Dyker H.Raabe G.Runsink J. Synlett 1992, 901 -
7a
Xu X.Wang J.Grison C.Petek S.Coutrot P.Birck M.Woodard RW.Gatti D. Drug Des. Discov. 2003, 18: 1 -
7b
Petek S. Ph.D. Thesis University of Nancy 1; France: 2003. -
7c
Coutrot P.Grison C.Tabyaoui M.Tabyaoui B.Dumarçay S. Synlett 1999, 792 -
7d
Coutrot P.Grison C.Tabyaoui M.Tabyaoui B.Dumarçay S. Bioorg. Med. Chem. Lett. 1999, 9: 949 -
7e
Dumarçay S. Ph.D. Thesis University of Nancy 1; France: 1998. -
7f
Coutrot P.Grison C.Tabyaoui M. Tetrahedron Lett. 1993, 34: 5089 -
8a
Coutrot P.Grison C.Tabyaoui M.Czernecki S.Valery JM. J. Chem. Soc., Chem. Commun. 1988, 1515 -
8b
Coutrot P.Legris C. Synthesis 1975, 118 - 10
Villieras J.Castro B.Ferracutti N. Bull. Soc. Chim. 1970, 1450 - 11
Seneci P.Leger I.Souchet M.Nadler G. Tetrahedron 1997, 53: 17097
References
Present address: Laboratoire de Chimie Biomoléculaire, UMR CNRS - UM II - Mayoly Spindler 5032 - ERT 5, Université Montpellier II, ENSCM, 8 Rue de l"Ecole Normale, 34296 Montpellier, France.
9
Experimental Procedure: In a typical experiment to obtain 5d, Mg (powder 325 mesh, 20.3 mmol) was poured onto anhyd Et2O (65 mL). Iodine (10.15 mmol) was added onto the mixture. After stirring at 35 °C during 3 h in the absence of light, the mixture MgI2-activated Mg was allowed to warm to r.t. and was added dropwise, at -60 °C under stirring, to the α-chloroglycidic ester 1 (10.15 mmol) at the concentration of 0.05 M in Et2O-toluene 4:1.
[10]
The mixture was allowed to warm up to -30 °C. After stirring during 120 min, HMPA (40.60 mmol) and Et3N (30.15 mmol) were added before adding a solution of CH3OCH2Cl (20.30 mmol) in Et2O (10 mL). The resulting mixture was stirred for 6 h at r.t. and H2O (15 mL) was added. The mixture was extracted with Et2O (2 × 15 mL), the combined organic extract was dried with MgSO4, the solvent was removed under reduced pressure, and the residue purified by silica gel column chromatography to afford 5.
Analytical Data of (
Z
)-5d: FTIR (KBr plate): 1721, 1660 cm-1. 1H NMR (250 MHz, CDCl3): δ = 1.26 (d, 3 H, J = 6 Hz), 1.27 (d, 3 H, J = 6 Hz), 1.32, 1.47, 1.66 (3 s, 12 H), 3.47 (s, 3 H), 4.25 (dd, 1 H, J = 7.9 Hz, J = 1.6 Hz), 4.30 (dd, 1 H, J = 4.7 Hz, J = 2.0 Hz), 4.60 (dd, 1 H, J = 2.0 Hz, J = 7.9 Hz), 4.89 (dd, 1 H, J = 1.6 Hz, J = 8.3 Hz), 4.90-5.15 (2 m, 3 H), 5.52 (d, J = 4.7 Hz), 6.27 (d, 1 H, J = 8.3 Hz). 13C NMR (62.9 MHz, CDCl3): δ = 21.4, 24.0, 24.6, 25.6, 57.1, 63.1, 68.7, 70.1, 70.5, 72.5, 96.1, 97.0, 108.3, 109.0, 122.6, 143.9, 162.2. MS (FAB+): m/z = 403 (65) [M + 1].