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Enantiospecific Stereodivergent Synthesis of trans- and cis-N(2),3-Dimethyl-4-phenyl-1,2,3,4-tetrahydroisoquinolines

Chemistry, an Asian journal, 2010-03, Vol.5 (3), p.589-604

2010

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Deprotonation-electrophile trapping of terminal epoxides

Organic & biomolecular chemistry, 2005-05, Vol.3 (10), p.1893-1904

2005

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Synthesis and C-Alkylation of Hindered Aldehyde Enamines

Journal of organic chemistry, 2009-02, Vol.74 (3), p.1019-1028

2009

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Substituted Epoxides by Lithiation of Terminal Epoxides

Organic letters, 2004-11, Vol.6 (23), p.4187-4189

2004

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Enantioselective synthesis of succinic acids and γ-lactones via palladium catalysed allylic substitution reactions

Tetrahedron: asymmetry, 1995-10, Vol.6 (10), p.2535-2546

1995

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Palladium catalysed allylic substitution reactions of prochiral and racemic allyl acetates

Tetrahedron letters, 1995-01, Vol.36 (3), p.461-462

1995

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Thrombin inhibitors based on [5,5] trans-fused indane lactams

Bioorganic & medicinal chemistry letters, 1999-06, Vol.9 (12), p.1657-1662

1999

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The tandem insertion of trimethylsilylcyanide and alkenes, alkynes, isocyanates or ketones into zirconacyclo-pentanes and -pentenes

Tetrahedron letters, 1995-06, Vol.36 (23), p.4113-4116

1995

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3-substituted-1,2,4-oxadiazolin-5-one; A useful amidine precursor and protecting group

Tetrahedron letters, 1995-06, Vol.36 (25), p.4471-4474

1995

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Synthesis of trans-fused [5,5] bicyclic lactones/lactams as templates for serine protease inhibition

Tetrahedron letters, 1998-09, Vol.39 (38), p.6979-6982

1998

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Asymmetric palladium catalysed allylic substitution using phosphorus containing oxazoline ligands

Tetrahedron letters, 1993-05, Vol.34 (19), p.3149-3150

1993

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Straightforward synthesis of α,β-epoxysilanes from terminal epoxides by lithium 2,2,6,6-tetramethylpiperidide-mediated deprotonation-in situ silylation

Tetrahedron letters, 2002-10, Vol.43 (44), p.7895-7897

2002

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Tricarbonylchromium(O) promoted stereoselective transformations of ephedrine and pseudoephedrine derivatives

Tetrahedron: asymmetry, 1990, Vol.1 (11), p.817-842

1990

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Preparation of novel Sulfur and phosphorus containing oxazolines as ligands for asymmetric catalysis

Tetrahedron, 1994-01, Vol.50 (3), p.799-808

1994

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Zirconocene-Mediated Synthesis of 3,4-Disubstituted Piperidines and Reduced Isoquinolines

Synthesis (Stuttgart), 1998, Vol.1998 (Sup. 1), p.557-568

Kemp, Mark I.

1998

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Early Transition Metal Induced Intramolecular Cocyclisation/Elaboration Reactions Using a Cleavable Silicon Linker

Synlett, 1997-12, Vol.12 (12), p.1371-1374

1997

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Sulfides tethered to oxazolines: Ligands for enantioselective catalysis

Tetrahedron letters, 1993-11, Vol.34 (48), p.7793-7796

1993

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Synthetic [5,5] trans-fused indane lactones as inhibitors of thrombin

Bioorganic & medicinal chemistry letters, 1999-02, Vol.9 (3), p.431-436

1999

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A Zirconium-Mediated Synthesis of (±)-Tecomanine

Synthesis (Stuttgart), 1998, Vol.1998 (Sup. 1), p.552-556

Kemp, Mark I.

1998

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Complementary stereoselective cyclisations of N-(3,4-dimethoxybenzyl)ephedrine and its chromium tricarbonyl complex to trans- and cis-2,3-dimethyl-4-phenyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolines respectively

Journal of the Chemical Society. Chemical communications, 1988 (10), p.648-649

1988

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The Preparation of Functionalised Aryl Phosphines from Aryl Fluorides by Nucleophilic Aromatic Substitution with Potassium Diphenylphosphide

Synlett, 1993, Vol.1993 (7), p.509-510

1993

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Zirconocene-Mediated Synthesis of 3,4-Disubstituted Piperidines and Reduced Isoquinolines

Synlett, 1994, Vol.1994 (6), p.451-453

1994

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Tricarbonylchromium(0) promoted stereoselective cyclisations of the N-3,4-dimethoxyphenethyl derivatives of the 1-phenyl ethanolamines halostachine, ephedrine and pseudoephedrine to 1-phenyl- N-methyl-7,8-dimethoxy-1,2,4,5-tetrahydrobenzazepines

Tetrahedron: asymmetry, 1990, Vol.1 (1), p.33-56

1990

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Enantiospecific synthesis of (+)-(R)-1-phenyl-3-methyl-1,2,4,5-tetrahydrobenz[d]azepine from (+)-(S)-N-methyl-1-phenyl ethanolamine (halostachine) via arene chromium tricarbonyl methodology

Tetrahedron letters, 1989, Vol.30 (27), p.3581-3588

1989

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5-Bromobarbituric Acid : A Mild and Selective Monobrominating Agent Employed in the Synthesis of the Gastrin Antagonist GR174152

Synthetic communications, 1996-11, Vol.26 (22), p.4195-4209

1996

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Enantiospecific Stereodivergent Synthesis of trans- and cis-N(2),3-Dimethyl-4-phenyl-1,2,3,4-tetrahydroisoquinolines

Deprotonation-electrophile trapping of terminal epoxides

Synthesis and C-Alkylation of Hindered Aldehyde Enamines

Substituted Epoxides by Lithiation of Terminal Epoxides

Enantioselective synthesis of succinic acids and γ-lactones via palladium catalysed allylic substitution reactions

Palladium catalysed allylic substitution reactions of prochiral and racemic allyl acetates

Thrombin inhibitors based on [5,5] trans-fused indane lactams

The tandem insertion of trimethylsilylcyanide and alkenes, alkynes, isocyanates or ketones into zirconacyclo-pentanes and -pentenes

3-substituted-1,2,4-oxadiazolin-5-one; A useful amidine precursor and protecting group

Synthesis of trans-fused [5,5] bicyclic lactones/lactams as templates for serine protease inhibition

Asymmetric palladium catalysed allylic substitution using phosphorus containing oxazoline ligands

Straightforward synthesis of α,β-epoxysilanes from terminal epoxides by lithium 2,2,6,6-tetramethylpiperidide-mediated deprotonation-in situ silylation

Tricarbonylchromium(O) promoted stereoselective transformations of ephedrine and pseudoephedrine derivatives

Preparation of novel Sulfur and phosphorus containing oxazolines as ligands for asymmetric catalysis

Zirconocene-Mediated Synthesis of 3,4-Disubstituted Piperidines and Reduced Isoquinolines

Early Transition Metal Induced Intramolecular Cocyclisation/Elaboration Reactions Using a Cleavable Silicon Linker

Sulfides tethered to oxazolines: Ligands for enantioselective catalysis

Synthetic [5,5] trans-fused indane lactones as inhibitors of thrombin

A Zirconium-Mediated Synthesis of (±)-Tecomanine

Complementary stereoselective cyclisations of N-(3,4-dimethoxybenzyl)ephedrine and its chromium tricarbonyl complex to trans- and cis-2,3-dimethyl-4-phenyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolines respectively

The Preparation of Functionalised Aryl Phosphines from Aryl Fluorides by Nucleophilic Aromatic Substitution with Potassium Diphenylphosphide

Zirconocene-Mediated Synthesis of 3,4-Disubstituted Piperidines and Reduced Isoquinolines

Tricarbonylchromium(0) promoted stereoselective cyclisations of the N-3,4-dimethoxyphenethyl derivatives of the 1-phenyl ethanolamines halostachine, ephedrine and pseudoephedrine to 1-phenyl- N-methyl-7,8-dimethoxy-1,2,4,5-tetrahydrobenzazepines

Enantiospecific synthesis of (+)-(R)-1-phenyl-3-methyl-1,2,4,5-tetrahydrobenz[d]azepine from (+)-(S)-N-methyl-1-phenyl ethanolamine (halostachine) via arene chromium tricarbonyl methodology

5-Bromobarbituric Acid : A Mild and Selective Monobrominating Agent Employed in the Synthesis of the Gastrin Antagonist GR174152

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