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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 (Stuttgart), 1995-08, Vol.1995 (8), p.1014-1018

1995

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Asymmetric Hydrogenation of 2-Benzylidenesuccinic Acid 4-[(4-BOC-amino)-1-piperidide] Monoamide: Key Step in a Process for Large Scale Preparation of a Renin Inhibitor

Synthesis (Stuttgart), 1994, Vol.1994 (5), p.494-498

Jendralla, Heiner

1994

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Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor

Tetrahedron letters, 1990, Vol.31 (18), p.2545-2548

1990

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Synthesis and biological activity of new HMG-CoA reductase inhibitors. 2. Derivatives of 7-(1H-pyrrol-3-yl)-substituted-3,5-dihydroxyhept-6(E)-enoic (-heptanoic) acids

Journal of medicinal chemistry, 1990-01, Vol.33 (1), p.61-70

1990

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Synthesis and biological activity of new HMG-CoA reductase inhibitors. 1. Lactones of pyridine- and pyrimidine-substituted 3,5-dihydroxy-6-heptenoic (-heptanoic) acids

Journal of medicinal chemistry, 1990-01, Vol.33 (1), p.52-60

1990

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Synthesis and biological activity of new HMG-CoA reductase inhibitors. 3. Lactones of 6-phenoxy-3,5-dihydroxyhexanoic acids

Journal of medicinal chemistry, 1991-10, Vol.34 (10), p.2962-2983

1991

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The influence of endocyclic oxygen atoms on the cycloaddition reactivity of trans-cyclo-octene

Tetrahedron, 1983, Vol.39 (8), p.1359-1363

Jendralla, H.

1983

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Carbocyclic Three- and Four Membered Ring Compounds

4th Edition.

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Carbocyclic Three- and Four-Membered Ring Compounds

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Vanadium(II)- and Niobium(III)-Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to C2-Symmetrical HIV-Protease Inhibitors

Angewandte Chemie (International ed.), 1994-03, Vol.33 (6), p.685-687

1994

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Asymmetric hydrogenation of itaconic acids with rhodium(I)-phenyl-capp complex a correction

Tetrahedron letters, 1991-07, Vol.32 (30), p.3671-3672

Jendralla, Heiner

1991

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Asymmetric CC - hydrogenation of a substrate with sulfur functionality. Influence of solvent and substrate configuration on enantioselectivity

Tetrahedron: asymmetry, 1994-07, Vol.5 (7), p.1183-1186

Jendralla, Heiner

1994

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Syntheses of 4(R)-silyloxy-6(S)-iodomethyl-tetrahydropyran-2-one and its enantiomer, building blocks for HMG-COA reductase inhibitors

Tetrahedron letters, 1988, Vol.29 (21), p.2563-2565

1988

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Enantioselective synthesis of a new fluoro-substituted HMG-COA reductase inhibitor

Tetrahedron letters, 1989, Vol.30 (38), p.5115-5118

1989

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Efficient synthesis of ( R)- and ( S)-(6,6′-difluorobiphenyl-2,2′-diyl) bis(diphenylphosphine); electron-poor biphenyl-type ligands for transition metal catalysts

Tetrahedron: asymmetry, 1994-07, Vol.5 (7), p.1297-1320

1994

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Vanadium( II )‐ and Niobium( III )‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to Give a C 2 ‐Symmetrical HIV Protease Inhibitor

Chemistry : a European journal, 1996-03, Vol.2 (3), p.307-315

1996

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Synthesis of a novel HMG-COA reductase inhibitor

Tetrahedron letters, 1988, Vol.29 (8), p.929-930

1988

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Effects of Leukotrienes on Gastric Acid and Alkaline Secretions

Gastroenterology (New York, N.Y. 1943), 1987-05, Vol.92 (5), p.1209-1214

1987

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Convenient two-step stereospecific hydroxy-substitution with retention in β-hydroxy-δ-lactones. 4 ( [formula omitted])-heterosubstituted mevinolin and -analogs

Tetrahedron letters, 1986, Vol.27 (39), p.4709-4712

1986

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Effects of leukotriene C4 on pancreatic secretion and circulation in dogs

American journal of physiology: Gastrointestinal and liver physiology, 1988-06, Vol.254 (6 Pt 1), p.G849-G855

1988

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Efficient kg-scale synthesis of Thrombin Inhibitor CRC 220

Tetrahedron, 1995-10, Vol.51 (44), p.12047-12068

1995

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Stereoselective synthesis of 2( S)-(1,1-dimethylethylsulfonylmethyl)-3-(1-naphthyl)-propionic acid, building block for protease inhibitors via asymmetric hydrogenation

Tetrahedron, 1994-04, Vol.50 (16), p.4691-4698

1994

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Synthesis of substituted phenyl-, biphenyl-, and terphenylcarbaldehydes by coupling of arylpalladium complexes with alkyl- and aryl-grignard reagents

Liebigs Annalen der Chemie, 1991-03, Vol.1991 (3), p.295-297

Jendralla, Heiner

1991

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ChemInform Abstract: DEAMINATION OF N‐(2‐OXABICYCLO(4.1.0)HEPT‐7‐EXO‐YL)‐N‐NITROSOUREA. ATTEMPTED GENERATION OF A HETEROCYCLIC TRANS‐CYCLOHEPTENE DERIVATIVE

Chemischer Informationsdienst, 1981-02, Vol.12 (6)

JENDRALLA, H.

1981

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Synthesis of 1,2,3,4,5,6-Hexahydropyrrolo[3,4-c]pyrrole Dihydrobromide and 1,2,3,5-Tetrahydro-2-[(4-methylphenyl)sulfonyl]pyrrolo[3,4-c]pyrrole

Heterocycles, 1995-06, Vol.41 (6), p.1291

1995

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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

Asymmetric Hydrogenation of 2-Benzylidenesuccinic Acid 4-[(4-BOC-amino)-1-piperidide] Monoamide: Key Step in a Process for Large Scale Preparation of a Renin Inhibitor

Stereoselective synthesis of HR 780 a new highly potent HMG-CoA reductase inhibitor

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 2. Derivatives of 7-(1H-pyrrol-3-yl)-substituted-3,5-dihydroxyhept-6(E)-enoic (-heptanoic) acids

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 1. Lactones of pyridine- and pyrimidine-substituted 3,5-dihydroxy-6-heptenoic (-heptanoic) acids

Synthesis and biological activity of new HMG-CoA reductase inhibitors. 3. Lactones of 6-phenoxy-3,5-dihydroxyhexanoic acids

The influence of endocyclic oxygen atoms on the cycloaddition reactivity of trans-cyclo-octene

Carbocyclic Three- and Four Membered Ring Compounds

Carbocyclic Three- and Four-Membered Ring Compounds

Vanadium(II)- and Niobium(III)-Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to C2-Symmetrical HIV-Protease Inhibitors

Asymmetric hydrogenation of itaconic acids with rhodium(I)-phenyl-capp complex a correction

Asymmetric CC - hydrogenation of a substrate with sulfur functionality. Influence of solvent and substrate configuration on enantioselectivity

Syntheses of 4(R)-silyloxy-6(S)-iodomethyl-tetrahydropyran-2-one and its enantiomer, building blocks for HMG-COA reductase inhibitors

Enantioselective synthesis of a new fluoro-substituted HMG-COA reductase inhibitor

Efficient synthesis of ( R)- and ( S)-(6,6′-difluorobiphenyl-2,2′-diyl) bis(diphenylphosphine); electron-poor biphenyl-type ligands for transition metal catalysts

Vanadium( II )‐ and Niobium( III )‐Induced, Diastereoselective Pinacol Coupling of Peptide Aldehydes to Give a C 2 ‐Symmetrical HIV Protease Inhibitor

Synthesis of a novel HMG-COA reductase inhibitor

Effects of Leukotrienes on Gastric Acid and Alkaline Secretions

Convenient two-step stereospecific hydroxy-substitution with retention in β-hydroxy-δ-lactones. 4 ( [formula omitted])-heterosubstituted mevinolin and -analogs

Effects of leukotriene C4 on pancreatic secretion and circulation in dogs

Efficient kg-scale synthesis of Thrombin Inhibitor CRC 220

Stereoselective synthesis of 2( S)-(1,1-dimethylethylsulfonylmethyl)-3-(1-naphthyl)-propionic acid, building block for protease inhibitors via asymmetric hydrogenation

Synthesis of substituted phenyl-, biphenyl-, and terphenylcarbaldehydes by coupling of arylpalladium complexes with alkyl- and aryl-grignard reagents

ChemInform Abstract: DEAMINATION OF N‐(2‐OXABICYCLO(4.1.0)HEPT‐7‐EXO‐YL)‐N‐NITROSOUREA. ATTEMPTED GENERATION OF A HETEROCYCLIC TRANS‐CYCLOHEPTENE DERIVATIVE

Synthesis of 1,2,3,4,5,6-Hexahydropyrrolo[3,4-c]pyrrole Dihydrobromide and 1,2,3,5-Tetrahydro-2-[(4-methylphenyl)sulfonyl]pyrrolo[3,4-c]pyrrole

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