Asymmetric Synthesis of Cα‐Substituted Prolines through Curtin–Hammett‐Controlled Diastereoselective N‐Alkylation-Reference-Cited by-同舟云学术

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Asymmetric Synthesis of Cα‐Substituted Prolines through Curtin–Hammett‐Controlled Diastereoselective N‐Alkylation

Published:2019-01-21 Issue:10 Volume:25 Page:2447-2451
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Cho Hyunkyung¹,Jeon Hongjun¹,Shin Jae Eui¹,Lee Seokwoo¹,Park Soojun¹,Kim Sanghee¹^ORCID

Affiliation:

1. College of PharmacySeoul National University 1 Gwanak-ro Gwanak-gu Seoul 08826 Korea

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201804965

Reference55 articles.

1.

2. Enantio- and diastereoselective syntheses of cyclic Cα-tetrasubstituted α-amino acids and their use to induce stable conformations in short peptides

3. Proline: The Distribution, Frequency, Positioning, and Common Functional Roles of Proline and Polyproline Sequences in the Human Proteome

4.

5. Influence of proline residues on protein conformation

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