Diastereoselective Pictet–Spengler condensation of tryptophan with α-amino aldehydes as chiral carbonyl components-Reference-Cited by-同舟云学术

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Diastereoselective Pictet–Spengler condensation of tryptophan with α-amino aldehydes as chiral carbonyl components

Published:2008-02 Issue:7 Volume:64 Page:1506-1514
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Pulka Karolina,Kulis Piotr,Tymecka Dagmara,Frankiewicz Lukasz,Wilczek Marcin,Kozminski Wiktor,Misicka Aleksandra

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. Über die Bildung von Isochinolin‐derivaten durch Einwirkung von Methylal auf Phenyl‐äthylamin, Phenyl‐alanin und Tyrosin

2. Conformational restriction of Tyr and Phe side chains in opioid peptides: Information about preferred and bioactive side‐chain topology

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

4. Towards control of χ-space: Conformationally constrained analogues of Phe, Tyr, Trp and His

5. Conformational and Topographical Considerations in Designing Agonist Peptidomimetics from Peptide Leads

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2. The stereospecific and enantiospecific synthesis of indole alkaloids which culminated in the ambidextrous Pictet–Spengler reaction for the C-19 methyl–substituted sarpagine family;Progress in Heterocyclic Chemistry;2021

3. Natural Product-Derived Chiral Pyrrolidine-2,5-diones, Their Molecular Structures and Conversion to Pharmacologically Important Skeletons;Journal of Natural Products;2020-06-25

4. Questioning the γ-gauche effect: stereoassignment of 1,3-disubstituted-tetrahydro-β-carbolines using 1H–1H coupling constants;Organic & Biomolecular Chemistry;2019

5. Unprecedented Stereocontrol in the Synthesis of 1,2,3-Trisubstituted Tetrahydro-β-carbolines through an Asymmetric Pictet-Spengler Reaction towards Sarpagine-Type Indole Alkaloids;European Journal of Organic Chemistry;2018-06-21

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