First syntheses of (2S, 3S)- and (2S, 3R)-m-prenyl-β-hydroxytyrosine derivatives: Bioactive amino acid fragment of a substance P antagonist novel cyclic heptapeptide-Reference-Cited by-同舟云学术

First syntheses of (2S, 3S)- and (2S, 3R)-m-prenyl-β-hydroxytyrosine derivatives: Bioactive amino acid fragment of a substance P antagonist novel cyclic heptapeptide

Published:1997-01 Issue:3 Volume:38 Page:473-476
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ravi Kumar Jalluri S.,Datta Apurba

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. Structure, determination, pharmacological evaluation, and structure-activity studies of a new cyclic peptide substance P antagonist containing the new amino acid 3-prenyl-.beta.-hydroxytyrosine isolated from Aspergillus flavipes

2. WIN 66306, a new neuroknin antagonist produced by an Aspergillus species: Fermentation, isolation and physico-chemical properties.

3. DIRECTED RING CLOSURE IN THE SYNTHESIS OF CHROMANS AND COUMARANS FROM o-ALLYLPHENOLS

4. The synthesis and configurational stability of differentially protected .beta.-hydroxy-.alpha.-amino aldehydes

5. An Improved Procedure for the Preparation of the Garner Aldehyde and Its Use for the Synthesis ofN-Protected 1-Halo-2-(R)-amino-3-butenes

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