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Induction of novel agonist selectivity for the ADP-activated P2Y1 receptor versus the ADP-activated P2Y12 and P2Y13 receptors by conformational constraint of an ADP analog

The Journal of pharmacology and experimental therapeutics, 2004-12, Vol.311 (3), p.1038

2004

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Unprecedented Acceleration of Zirconium(IV)-Assisted Peptide Hydrolysis at Neutral pH

Inorganic chemistry, 2004-10, Vol.43 (20), p.6130-6132

2004

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Methanocarba Modification of Uracil and Adenine Nucleotides: High Potency of Northern Ring Conformation at P2Y1, P2Y2, P2Y4, and P2Y11 but Not P2Y6 Receptors

Journal of medicinal chemistry, 2002-01, Vol.45 (1), p.208-218

2002

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Methanocarba Analogues of Purine Nucleosides as Potent and Selective Adenosine Receptor Agonists

Journal of medicinal chemistry, 2000-06, Vol.43 (11), p.2196-2203

2000

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Adenine Nucleotide Analogues Locked in a Northern Methanocarba Conformation: Enhanced Stability and Potency as P2Y1 Receptor Agonists

Journal of medicinal chemistry, 2002-05, Vol.45 (10), p.2090-2100

2002

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2‐Chloro N6‐methyl‐(N)‐methanocarba‐2′‐deoxyadenosine‐3′,5′‐bisphosphate is a selective high affinity P2Y1 receptor antagonist

British journal of pharmacology, 2002-04, Vol.135 (8), p.2004-2010

2002

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Potent P2X7 receptor antagonists: Tyrosyl derivatives synthesized using a sequential parallel synthetic approach

Drug development research, 2001-10, Vol.54 (2), p.75-87

2001

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Potent P2X 7 Receptor Antagonists: Tyrosyl Derivatives Synthesized Using a Sequential Parallel Synthetic Approach

Drug development research, 2001-10, Vol.54 (2), p.75-87

2001

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2‐Chloro N 6 ‐methyl‐(N)‐methanocarba‐2′‐deoxyadenosine‐3′,5′‐bisphosphate is a selective high affinity P2Y 1 receptor antagonist

British journal of pharmacology, 2009-02, Vol.135 (8), p.2004-2010

2009

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Adenine nucleotide analogues locked in a Northern methanocarba conformation: enhanced stability and potency as P2Y(1) receptor agonists

Journal of medicinal chemistry, 2002-05, Vol.45 (10), p.2090-2100

2002

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Functionalized Congeners of Tyrosine-Based P2X7 Receptor Antagonists: Probing Multiple Sites for Linking and Dimerization

Bioconjugate chemistry, 2002-09, Vol.13 (5), p.1100-1111

2002

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Asymmetric Allylation and Reduction on an Ephedrine-Derived Template: Stereoselective Synthesis of α-Hydroxy Acids and Derivatives

Journal of organic chemistry, 1998-06, Vol.63 (12), p.4120-4124

1998

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Asymmetric reactions of α-ketoacid-derived hemiacetals: Stereoselective synthesis of α-hydroxy acids

Tetrahedron, 1998-11, Vol.54 (48), p.14549-14564

1998

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Functionalized congeners of tyrosine-based P2X(7) receptor antagonists: probing multiple sites for linking and dimerization

Bioconjugate chemistry, 2002-09, Vol.13 (5), p.1100

2002

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Functionalized Congeners of Tyrosine-Based P2X 7 Receptor Antagonists: Probing Multiple Sites for Linking and Dimerization

Bioconjugate chemistry, 2002-09, Vol.13 (5), p.1100-1111

2002

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2-Chloro N(6)-methyl-(N)-methanocarba-2'-deoxyadenosine-3',5'-bisphosphate is a selective high affinity P2Y(1) receptor antagonist

British journal of pharmacology, 2002-04, Vol.135 (8), p.2004

2002

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Adenine Nucleotide Analogues Locked in a Northern Methanocarba Conformation: Enhanced Stability and Potency as P2Y 1 Receptor Agonists

Journal of medicinal chemistry, 2002-05, Vol.45 (10), p.2090-2100

2002

Volltextzugriff (PDF)

Methanocarba Modification of Uracil and Adenine Nucleotides: High Potency of Northern Ring Conformation at P2Y 1 , P2Y 2 , P2Y 4 , and P2Y 11 but Not P2Y 6 Receptors

Journal of medicinal chemistry, 2002-01, Vol.45 (1), p.208-218

2002

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Stereodivergent Approach to α-Hydroxy Acids Involving Substrate Directed Reduction of α-Keto Amides

Tetrahedron letters, 1995-08, Vol.36 (33), p.5959-5962

Pansare, S

1995

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Asymmetric synthesis of α-alkyl-α-hydroxy-γ-butyrolactones

Tetrahedron: asymmetry, 1999-08, Vol.10 (16), p.3103-3106

1999

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Stereodivergent approach to α-hydroxy acids involving substrate directed reduction of α-keto amides

Tetrahedron letters, 1995-08, Vol.36 (33), p.5959-5962

1995

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Steric and Electronic Effects in Arene Formylations involving Pyrophosphoryl Chloride

Synlett, 1994-10, Vol.1994 (10), p.823-824

1994

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Structurally related nucleotides as selective agonists and antagonists at P2Y1 receptors

Farmaco (Società chimica italiana : 1989), 2001-01, Vol.56 (1-2), p.71-75

2001

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ChemInform Abstract: Asymmetric Reactions of α-Ketoacid-Derived Hemiacetals: Stereoselective Synthesis of α-Hydroxy Acids

ChemInform, 1999-03, Vol.30 (13), p.no-no

1999

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ChemInform Abstract: Asymmetric Synthesis of α-Alkyl-α-hydroxy-γ-butyrolactones

ChemInform, 2000-01, Vol.31 (3), p.no-no

2000

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Induction of novel agonist selectivity for the ADP-activated P2Y1 receptor versus the ADP-activated P2Y12 and P2Y13 receptors by conformational constraint of an ADP analog

Unprecedented Acceleration of Zirconium(IV)-Assisted Peptide Hydrolysis at Neutral pH

Methanocarba Modification of Uracil and Adenine Nucleotides: High Potency of Northern Ring Conformation at P2Y1, P2Y2, P2Y4, and P2Y11 but Not P2Y6 Receptors

Methanocarba Analogues of Purine Nucleosides as Potent and Selective Adenosine Receptor Agonists

Adenine Nucleotide Analogues Locked in a Northern Methanocarba Conformation: Enhanced Stability and Potency as P2Y1 Receptor Agonists

2‐Chloro N6‐methyl‐(N)‐methanocarba‐2′‐deoxyadenosine‐3′,5′‐bisphosphate is a selective high affinity P2Y1 receptor antagonist

Potent P2X7 receptor antagonists: Tyrosyl derivatives synthesized using a sequential parallel synthetic approach

Potent P2X 7 Receptor Antagonists: Tyrosyl Derivatives Synthesized Using a Sequential Parallel Synthetic Approach

2‐Chloro N 6 ‐methyl‐(N)‐methanocarba‐2′‐deoxyadenosine‐3′,5′‐bisphosphate is a selective high affinity P2Y 1 receptor antagonist

Adenine nucleotide analogues locked in a Northern methanocarba conformation: enhanced stability and potency as P2Y(1) receptor agonists

Functionalized Congeners of Tyrosine-Based P2X7 Receptor Antagonists: Probing Multiple Sites for Linking and Dimerization

Asymmetric Allylation and Reduction on an Ephedrine-Derived Template: Stereoselective Synthesis of α-Hydroxy Acids and Derivatives

Asymmetric reactions of α-ketoacid-derived hemiacetals: Stereoselective synthesis of α-hydroxy acids

Functionalized congeners of tyrosine-based P2X(7) receptor antagonists: probing multiple sites for linking and dimerization

Functionalized Congeners of Tyrosine-Based P2X 7 Receptor Antagonists: Probing Multiple Sites for Linking and Dimerization

2-Chloro N(6)-methyl-(N)-methanocarba-2'-deoxyadenosine-3',5'-bisphosphate is a selective high affinity P2Y(1) receptor antagonist

Adenine Nucleotide Analogues Locked in a Northern Methanocarba Conformation: Enhanced Stability and Potency as P2Y 1 Receptor Agonists

Methanocarba Modification of Uracil and Adenine Nucleotides: High Potency of Northern Ring Conformation at P2Y 1 , P2Y 2 , P2Y 4 , and P2Y 11 but Not P2Y 6 Receptors

Stereodivergent Approach to α-Hydroxy Acids Involving Substrate Directed Reduction of α-Keto Amides

Asymmetric synthesis of α-alkyl-α-hydroxy-γ-butyrolactones

Stereodivergent approach to α-hydroxy acids involving substrate directed reduction of α-keto amides

Steric and Electronic Effects in Arene Formylations involving Pyrophosphoryl Chloride

Structurally related nucleotides as selective agonists and antagonists at P2Y1 receptors

ChemInform Abstract: Asymmetric Reactions of α-Ketoacid-Derived Hemiacetals: Stereoselective Synthesis of α-Hydroxy Acids

ChemInform Abstract: Asymmetric Synthesis of α-Alkyl-α-hydroxy-γ-butyrolactones

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