Diastereoface differentiation in addition of lithium enolates to chiral α,β-epoxyaldehydes

[1]  K. Beresford,et al.  Asymmetric synthesis via nucleophilic addition to α,β-epoxyimines , 1992 .

[2]  G. P. Howe,et al.  Stereoselective reactions of α,β-epoxy-aldehydes; the formation of “chelation controlled” products , 1992 .

[3]  M. Baltas,et al.  Diastereoselection in the addition of enolates to chiral α,β-epoxyaldehydes , 1991 .

[4]  A. Jacot‐Guillarmod,et al.  Synthése enantiospécifique du (-)-(1S,3R,5R)-1,8-diméthyl-3-éthyl-2,9-dioxabicyclo[3.3.1]non-7-éne , 1991 .

[5]  D. Grandjean,et al.  Synthesis of optically pure cis epoxyalcohols via an enzymatic route; an alternative to the sharpless epoxidation. , 1991 .

[6]  M. VanNieuwenhze,et al.  A STEREOCHEMICALLY GENERAL SYNTHESIS OF 2-DEOXYHEXOSES VIA THE ASYMMETRIC ALLYLBORATION OF 2,3-EPOXY ALDEHYDES , 1991 .

[7]  E. Carreira,et al.  Synthesis of 1,3-diol synthons from epoxy aromatic precursors: an approach to the construction of polyacetate-derived natural products , 1991 .

[8]  R. Galarini,et al.  Stereoselective synthesis of 3-(ethoxycarbonyl)-4-hydroxy-5-(1-hydroxyalkyl)-2-isoxazoline 2-oxides by reaction of 2,3-epoxy aldehydes and ethyl nitroacetate on alumina surface , 1990 .

[9]  Anthony W. Czarnik,et al.  Chelation enhanced fluorescence in 9,10-bis[[(2-(dimethylamino)ethyl)methylamino]methyl]anthracene , 1988 .

[10]  S. Danishefsky,et al.  Stereoselective total syntheses of the naturally occurring enantiomers of N-acetylneuraminic acid and 3-deoxy-D-manno-2-octulosonic acid. A new and stereospecific approach to sialo and 3-deoxy-D-manno-2-octulosonic acid conjugates , 1988 .

[11]  K. Sharpless,et al.  Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization , 1987 .

[12]  R. W. Hoffmann Stereoselective Syntheses of Building Blocks with Three Consecutive Stereogenic Centers: Important Precursors of Polyketide Natural Products [New Synthetic Methods (68)] , 1987 .

[13]  J. Chong,et al.  Facile preparation of (2R,3S)- and (2S,3R)-3-[[(4-bromobenzyl)oxy]methyl]oxirane-2-methanol via asymmetric epoxidation , 1987 .

[14]  S. Danishefsky,et al.  Totally Synthetic Routes to the Higher Monosaccharides , 1987 .

[15]  G. P. Howe,et al.  Stereoselective additions to α,β-epoxy-aldehydes; the formation of “non-chelation controlled” products , 1987 .

[16]  Takashi Matsumoto,et al.  Synthesis of optically active .beta.,.gamma.-epoxy alcohols and secondary allylic alcohols via diastereoselective addition of .alpha.-(trimethylsilyl)-.alpha.,.beta.-epoxy aldehydes with organometallic compounds , 1986 .

[17]  K. Sharpless,et al.  Procedure for the catalytic asymmetric epoxidation of allylic alcohols in the presence of molecular sieves , 1986 .

[18]  J. Petersen,et al.  Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis , 1985 .

[19]  M. Reetz Chelation or Non‐Chelation Control in Addition Reactions of Chiral α‐ and β‐ Alkoxy Carbonyl Compounds [New Synthetic Methods (44)] , 1984 .

[20]  K. Prasad,et al.  Asymmetric synthesis of (3R-trans)-and (3S-cis)-hydroxy-5-pentanolides , 1984 .

[21]  W. Roush,et al.  Total synthesis of carbohydrates. 2. Regiochemical control of nucleophilic ring opening of acylated 2,3-epoxy alcohols , 1983 .

[22]  J. Dunitz,et al.  Stereochemistry of reaction paths at carbonyl centres , 1974 .

[23]  W. Doering,et al.  Sulfur trioxide in the oxidation of alcohols by dimethyl sulfoxide , 1967 .