References
1 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.
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
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].
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