Tetrahedron: Asymmetry report number 14Synthetic routes to 2,5-disubstituted tetrahydrofurans
2,5-Disubstituted tetrahydrofurans are structural features commonly encountered in many natural products. The preparation of such valuable synthetic units, because of their implications in biological processes, has attracted particular attention from the organic synthetic chemists. The purpose of this review is to present in a concise format the main preparations of 2,5-disubstituted tetrahydrofurans, and to report the recent progresses in the stereocontrolled routes to such units.
References (90)
Tetrahedron
(1987)- et al.
Tetrahedron
(1965)et al.J. Am. Chem. Soc.
(1979)et al.J. Chem. Soc.
(1979)et al.J. Am. Chem. Soc.
(1981) - et al.
Tetrahedron Lett.
(1980) - et al.
J. Am. Chem. Soc.
(1987) - et al.
J. Am. Chem. Soc.
(1991) - et al.
Tetrahedron Lett.
(1987)et al.Tetrahedron Lett.
(1988)et al.Chemistry Lett.
(1988)et al.Chemistry Lett.
(1988)et al.J. Org. Chem.
(1984) - et al.
J. Am. Chem. Soc.
(1990) - et al.
Tetrahedron Lett.
(1992) - et al.
J. Org. Chem.
(1988)et al.J. Org. Chem.
(1991) - et al.
J. Am. Chem. Soc.
(1981)
Carbohydrate Res.
(1987)
Tetrahedron Lett.
(1985)
Tetrahedron
(1991)
J. Am. Chem. Soc.
(1989)
J. Am. Chem. Soc.
(1992)
J. Am. Chem. Soc.
(1984)
Tetrahedron Lett.
(1992)
J. Org. Chem.
(1989)
Helvetica Chemica Acta
(1991)
J. Org. Chem.
(1981)
J. Chem. Soc., Perkin
(1974)
et al.J. Chem. Soc., Perkin
(1975)
Tetrahedron
(1991)
Chemistry Lett.
(1984)
et al.Carbohydrate Res.
(1987)
J. Org. Chem.
(1988)
Tetrahedron Lett.
(1987)
J. Am. Chem. Soc.
(1988)
et al.Tetrahedron Lett.
(1985)
J. Am. Chem. Soc.
(1987)
Tetrahedron
(1990)
Tetrahedron Lett.
(1988)
Carbohydrate Res.
(1987)
J. Chem. Soc.
(1983)
et al. et al.J. Chem. Soc.
(1984)
et al.J. Org. Chem.
(1985)
et al.Carbohydrate Res.
(1987)
J. Am. Chem. Soc.
(1991)
The total syhthesis of macrocyclic lactones
(1988)
Synthesis of naturally occurring C-nucleosides their analogs, and functionalized C-glycosyl precursors
Advances in carbohydrate chemistry and biochemistry
(1976)
Tetrahedron Lett.
(1992)
Tetrahedron Lett.
(1992)
J. Am. Chem. Soc.
(1975)
J. Am. Chem. Soc.
(1985)
et al.Carbohydrate Res.
(1987)
J. Am. Chem. Soc.
(1991)
et al.J. Am. Chem. Soc.
(1991)
(1982)
Tetrahedron
(1992)
J. Chem. Soc.
(1990)
J. Am. Chem. Soc.
(1987)
et al.J. Org. Chem.
(1990)
J. Am. Chem. Soc.
(1980)
J. Org. Chem.
(1962)
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