References
- Graul , A. and Castaner , J. 1997 . Atorvastatin. Drugs Fut. , 22 : 956 – 968 .
- Brower , P.L. , Butler , D.E. , Deering , C.F. , Le Tung , V. , Millar , A. , Nanninga , T.N. and Roth , B.D. 1992 . The synthesis of (4R-cis)-1, 1-dimethylethyl-6-cyanomethyl-2, 2-dimethyl-1, 3-dioxane-4-acetate, a key intermediate for the preparation of CI-981, a highly potent, tissue selective inhibitor of HMG-CoA reductase . Tetrahedron Lett. , 33 ( 17 ) : 2279 – 2282 .
- Baumann , K.L , Butler , D.E. , Deering , C.F. , Mennen , K.E. , Millar , A. , Nanninga , T.N. , Palmer , C.W. and Roth , B.D. 1992 . The convergent synthesis of CI-981, an optically active, highly potent, tissue selective inhibitor of HMG-CoA reductase . Tetrahedron Lett. , 33 ( 17 ) : 2283 – 2284 .
- Butler , D.E. and Millar , A. Process for the Synthesis of (4R-cis)-1, 1-Dimethylethyl 6-cyanomethyl-2, 2-dimethyl-1, 3-dioxane-4-acetate . US Patent 5,103,024 . April 07, 1992 . (Warner-Lambert Co.)
- Butler , D.E. , Le Tung , V. , Millar , A. and Nanninga , T.N. Process for the Synthesis of (5R)-1, 1-Dimethylethyl 6-cyano-5-hydroxy-3-oxo-hexanoate . US Patent 5,155,251 . October 13, 1992 . (Warner-Lambert Co.)
- Mitsuda , M , Miyazaki , M. and Inoue , K. Process for producing 6-cyanomethyl-2-dimethyl-1, 3-dioxane-4-acetic acid derivatives . EP Appl. 1,077, 212 A1 . April 28, 1999 . (Kaneka Co.)
- Wess , G. , Kesseler , K. , Baader , E. , Bartmann , W. , Beck , G. , Bergmann , A. , Jendralla , H. , Bock , K. , Holzstein , G. , Kleine , H. and Schneirer , M. 1990 . Stereoselective synthesis of HR 780, a new highly potent HMG-CoA reductase inhibitor . Tetrahedron Lett. , 31 ( 18 ) : 2545 – 2548 .
- Beck , G. , Jendralla , H. and Kesseler , K. 1995 . Practical large scale synthesis of tert-butyl (3R,5S)-6-hydroxy-3,5-O-isopropylidene-3,5-dihydroxyhexanoate: essential building block for HMG-CoA reductase inhibitors . Synthesis , 8 : 1014 – 1018 .
- Nishiyama , A. , Horikawa , M. , Yasohara , Y. , Ueyama , N. and Inoue , K. Process for preparing optically active 2-[6-(hydroxymethyl)-1,3-dioxan-4-yl]acetic acid derivatives . WO 01/94,337 . December 13, 2001 . (Kaneka Co)
- Masamune , S. , Ma , P. , Okumoto , H , Ellingboe , J.W. and Ito , Y. 1984 . Synthesis of amphotericin B. 1. fragment A of the aglycon . J. Org. Chem. , 49 ( 15 ) : 2834 – 2837 .
- de Raadt , A. , Griengl , H. and Klempier , N. 1993 . A mild and simple enzymatic conversion of aldono- and aldurononitriles into the corresponding amides and/or carboxylic acids . J. Org. Chem. , 58 ( 11 ) : 3179 – 3184 .
- Hiyama , T. , Minami , T. and Takahashi , K. 1995 . Synthesis of artificial HMG-CoA reductase inhibitors based on the olefination strategy . Bull. Soc. Chem. Jpn. , 68 ( 1 ) : 364 – 372 .
- Mancuso , A.J. and Swern , D. 1981 . Activated dimethyl sulfoxide: useful reagents for synthesis . Synthesis , : 165 – 185 .
- Mancuso , A.J. , Huang , S.-L. and Swern , D. 1978 . Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide activated by oxalyl chloride . J. Org. Chem. , 43 ( 12 ) : 2480 – 2482 .
- Cheng , Y.S. , Liu , W.-L. and Chen , S.H. 1980 . Pyridinium chlorochromate adsorbed on alumina as a selective oxidant for primary and secondary alcohols . Synthesis , 3 : 223 – 224 .
- Kozikowski , A.P. and Li , C.-S. 1985 . A nitrile oxide based entry to 2,3-dihydropyran-4-ones. Synthesis of a protected version of “compactin lactone” in racemic and optically active forms . J. Org. Chem. , 50 ( 6 ) : 778 – 785 .
- Kozikowski , A.P. , Kitagawa , Y. and Springer , J.P. 1983 . An examination of the extent of diastereofacial selection in the reactions of a chiral nitrile oxide with achiral alkenes: a route to β-hydroxy carboxylic acids . J. Chem. Soc., Chem. Commun. , 23 : 1460 – 1462 .
- Wollenberg , R.H. and Miller , S.J. 1978 . Nitroalkane synthesis. A convenient method for aldehyde reductive nitromethylation . Tetrahedron Lett. , 19 : 3219 – 3222 .
- Schechter , H. , Ley , D.L. and Robertson , E.B. 1956 . Nitroalkanes from conjugated nitroalkenes by reduction with complex hydrides . J. Am. Chem. Soc. , 78 : 4984 – 4991 .