Synthesis of Azaylide‐Based Amphiphiles by the Staudinger Reaction-Reference-Cited by-同舟云学术

Synthesis of Azaylide‐Based Amphiphiles by the Staudinger Reaction

Published:2021-07 Issue:33 Volume:60 Page:17915-17919
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Yamashina Masahiro¹^ORCID,Suzuki Hayate¹,Kishida Natsuki²,Yoshizawa Michito²^ORCID,Toyota Shinji¹^ORCID

Affiliation:

1. Department of Chemistry School of Science Tokyo Institute of Technology 2-12-1 Ookayama, Meguro-ku Tokyo 152–8551 Japan

2. Laboratory for Chemistry and Life Science, Institute of Innovative Research Tokyo Institute of Technology 4259 Nagatsuta, Midori-ku Yokohama 226-8503 Japan

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202105094

Reference45 articles.

1. Micelles

2. Micelles

3. Covalently cross-linked amphiphilic block copolymer micelles

4. Power struggles in peptide-amphiphile nanostructures

5. Aromatic Micelles as a New Class of Aqueous Molecular Flasks

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ag₂₀ Nanoclusters with Surface Azides as an Easily Functionalized Platform for Diverse Chemical Applications;Small;2024-08-07

2. Efficient and Sustainable Electrosynthesis of N-Sulfonyl Iminophosphoranes by the Dehydrogenative P–N Coupling Reaction;JACS Au;2024-04-18

3. Phosphazenes;Organophosphorus Chemistry;2024-02-21

4. Azaylide-based gemini amphiphiles displaying unique self-assembling behavior via an even–odd effect of alkyl linker chain length;Soft Matter;2024

5. Click assembly through selective azaylide formation;Chemical Communications;2024