A new strategy for the synthesis of mevinic acid analogues

[1]  H. L. Goering,et al.  Alkylation of allylic derivatives. XIV: Relationship of double-bond configuration between reactant and product for cross-coupling reactions of Z-allylic carboxylates with organocopper reagents , 1989 .

[2]  R. Hungate,et al.  The total synthesis of avermectin A1a , 1989 .

[3]  J. Jacquesy,et al.  Mevinic acids and analogs : a novel efficient route to chiral synthons from 1,6-anhydro-D-glucose , 1989 .

[4]  C. Hadley,et al.  Synthesis and biological evaluation of a monocyclic, fully functional analogue of compactin. , 1989, Journal of medicinal chemistry.

[5]  B. Roth,et al.  Synthesis of a chiral synthon for the lactone portion of compactin and mevinolin , 1988 .

[6]  David R. Williams,et al.  Bromine as an oxidant for direct conversion of aldehydes to esters , 1988 .

[7]  C. Hadley,et al.  Total synthesis and biological evaluation of structural analogues of compactin and dihydromevinolin. , 1987, Journal of medicinal chemistry.

[8]  R. Frenette,et al.  Stereoselective synthesis of endo-1,3 dimethyl-2,9 dioxabicyclo[3-3.1] nonane , 1987 .

[9]  S. Valverde,et al.  A straightforward synthesis of L-lactones from D-glucose. A simple entry into L-sugars , 1987 .

[10]  A. Deana,et al.  Synthesis and utilization of the chiral synthon methyl 3-O-benzyl-2,4,6-trideoxy-6-iodo-.alpha.-D-erythro-hexopyranoside in the synthesis of a potent HMG-CoA reductase inhibitor , 1986 .

[11]  W. F. Hoffman,et al.  3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 3. 7-(3,5-Disubstituted [1,1'-biphenyl]-2-yl)-3,5-dihydroxy-6-heptenoic acids and their lactone derivatives. , 1986, Journal of Medicinal Chemistry.

[12]  B. E. Evans,et al.  3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors. 1. Structural modification of 5-substituted 3,5-dihydroxypentanoic acids and their lactone derivatives. , 1985, Journal of Medicinal Chemistry.

[13]  C. Heathcock,et al.  The synthesis of mevinic acids , 1986 .

[14]  Y. Chapleur,et al.  Stereospecific formation of carbon-carbon bonds in ethyl 4,6-di-O-acetyl-2,3-dideoxy-α-d-ribo-hex-3-enopyranoside , 1985 .

[15]  C. Nakamura,et al.  Mode of interaction of beta-hydroxy-beta-methylglutaryl coenzyme A reductase with strong binding inhibitors: compactin and related compounds. , 1985, Biochemistry.

[16]  M. Taschner,et al.  Synthetic and biological studies of compactin and related compounds. II: Synthesis of the lactone moiety of compactin , 1984 .

[17]  R. Wilhelm,et al.  The chemistry of higher order organocuprates , 1984 .

[18]  E. Erdik.  Tetrahedron Report Number 159 , 1984 .

[19]  S. Hanessian,et al.  Oxidation of Alcohols with N-Halosuccinimides-New and Efficient Variants , 1981 .

[20]  O. Mitsunobu.  The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products , 1981 .

[21]  R Monaghan,et al.  Mevinolin: a highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agent. , 1980, Proceedings of the National Academy of Sciences of the United States of America.

[22]  J. Levisalles,et al.  Chimie organometallique VIII. Reaction des organocuprates avec les acetates allyliques. Existence probable de complexes π-allyliques du cuivre , 1977 .

[23]  Y. Tsujita,et al.  ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium. , 1976, The Journal of antibiotics.

[24]  A. Brown,et al.  Crystal and molecular structure of compactin, a new antifungal metabolite from Penicillium brevicompactum. , 1976, Journal of the Chemical Society. Perkin transactions 1.

[25]  A. C. Richardson.  The synthesis of N-benzoyl-D-daunosamine , 1967 .

[26]  Prins Da.  Reduction of sugar epoxides to desoxysugars. , 1948 .