Diversity‐oriented Functionalization of Cyclodienes Through Selective Cycloaddition/Ring‐opening/Cross‐metathesis Protocols; Transformation of a “Flatland” into Three‐dimensional Scaffolds With Stereo‐ and Regiocontrol-Reference-Cited by-同舟云学术

Diversity‐oriented Functionalization of Cyclodienes Through Selective Cycloaddition/Ring‐opening/Cross‐metathesis Protocols; Transformation of a “Flatland” into Three‐dimensional Scaffolds With Stereo‐ and Regiocontrol

Published:2020-07-28 Issue:10 Volume:20 Page:1129-1141
ISSN:1527-8999
Container-title:The Chemical Record
language:en
Short-container-title:Chem. Rec.

Author:

Kiss Loránd¹²^ORCID,Benke Zsanett¹²,Remete Attila M.¹²,Fülöp Ferenc¹²³

Affiliation:

1. Institute of Pharmaceutical Chemistry University of Szeged H-6720 Szeged Eötvös u. 6 Hungary

2. University of Szeged, I nterdisciplinary Excellence Centre Institute of Pharmaceutical Chemistry H-6720 Szeged Eötvös u. 6 Hungary

3. MTA-SZTE Stereochemistry Research Group Hungarian Academy of Sciences H-6720 Szeged Eötvös u. 6 Hungary

Funder

Hungarian Research Foundation

GINOP

EU-funded Hungarian grant

Ministry of Human Capacities, Hungary

Publisher

Wiley

Subject

Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/tcr.202000070

Reference86 articles.

2. Highly functionalized cyclic β-amino acid moieties as promising scaffolds in peptide research and drug design

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4. α/β-Chimera peptide synthesis with cyclic β-sugar amino acids: the efficient coupling protocol

5. Design of Peptidic Foldamer Helices: A Stereochemical Patterning Approach

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