Single‐Step, Rapid, and Mild Synthesis of β‐Amino Acid N ‐Carboxy Anhydrides Using Micro‐Flow Technology-Reference-Cited by-同舟云学术

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Single‐Step, Rapid, and Mild Synthesis of β‐Amino Acid N ‐Carboxy Anhydrides Using Micro‐Flow Technology

Published:2019-11-28 Issue:1 Volume:15 Page:79-84
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Sugisawa Naoto¹²,Otake Yuma¹²^ORCID,Nakamura Hiroyuki¹^ORCID,Fuse Shinichiro¹³^ORCID

Affiliation:

1. Laboratory for Chemistry and Life ScienceInstitute of Innovative ResearchTokyo Institute of Technology 4259 Nagatsuta-cho Midori-ku Yokohama 226-8503 Japan

2. School of Life Science and TechnologyTokyo Institute of Technology 4259 Nagatsuta-cho Midori-ku Yokohama 226-8503 Japan

3. Present address: Department of Basic Medical SciencesGraduate School of Pharmaceutical SciencesNagoya University Furo-cho Chikusa-ku Nagoya 464-8601 Japan

Funder

Japan Society for the Promotion of Science

Naito Foundation

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.201901429

Reference58 articles.

1.

2. β-Peptides: From Structure to Function

3. The World ofβ- andγ-Peptides Comprised of Homologated Proteinogenic Amino Acids and Other Components

4. Application of alicyclic β-amino acids in peptide chemistry

5. Antimicrobial peptide mimics for improved therapeutic properties

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4. Continuous‐/Micro‐Flow Reactions Using Highly Electrophilic PCl₃ and POCl₃;ChemPlusChem;2023-06

5. Rapid and column-chromatography-free peptide chain elongation via a one-flow, three-component coupling approach;Chemical Science;2023

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