(Q58201433)

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Synthesis of a conformationally constrained tyrosine–glycine dipeptide mimetic: design of a potential substrate of Syk kinase

article by Paolo Ruzza et al published May 2002 in Tetrahedron Letters

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Synthesis of a conformationally constrained tyrosine–glycine dipeptide mimetic: design of a potential substrate of Syk kinase (English)

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Andrea Calderan

2

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Paolo Ruzza

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1

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Alessio Osler

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3

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Stefano Elardo

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4

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Gianfranco Borin

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5

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publication date

May 2002

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published in

Tetrahedron Letters

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volume

43

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issue

20

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page(s)

3769-3771

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cites work

Design of peptides, proteins, and peptidomimetics in chi space.

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Conformational restriction of Tyr and Phe side chains in opioid peptides: information about preferred and bioactive side-chain topology

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Synthesis and use of 3-amino-4-phenyl-2-piperidones and 4-amino-2-benzazepin-3-ones as conformationally restricted phenylalanine isosteres in renin inhibitors

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Efficient synthesis of (S)-4-phthalimido-1,3,4,5-tetrahydro-8-(2,6-dichlorobenzyloxy)- 3-oxo-2H-2-benzazepin-2-acetic acid (PHt-Hba(2,6-Cl2-Bn)-Gly-OH).

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Prototype Pictet−Spengler Reactions Catalyzed by Superacids. Involvement of Dicationic Superelectrophiles

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10.1016/S0040-4039(02)00635-4

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(Q58201433)

Synthesis of a conformationally constrained tyrosine–glycine dipeptide mimetic: design of a potential substrate of Syk kinase

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