Modification of alkyne-functionalized asymmetric phthalocyanines by CuI-catalyzed azide-alkyne cycloaddition-Reference-Cited by-同舟云学术

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Modification of alkyne-functionalized asymmetric phthalocyanines by CuI-catalyzed azide-alkyne cycloaddition

Published:2015-12 Issue:48 Volume:71 Page:9154-9160
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chen Xiaochun,Lu Chin-Wei,Huang Yiming,McGrath Dominic V.

Funder

National Science Foundation

Center for Interface Science: Solar Electric Materials (CIS:SEM), an Energy Frontier Research Center

U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference71 articles.

1. Phthalocyanines as Active Materials for Optical Limiting

2. Molecular Engineering of Peripherally And Axially Modified Phthalocyanines for Optical Limiting and Nonlinear Optics

3. Axially modified gallium phthalocyanines and naphthalocyanines for optical limiting

4. Role of Structural Factors in the Nonlinear Optical Properties of Phthalocyanines and Related Compounds

5. Porphyrins and phthalocyanines as materials for optical limiting

Cited by 6 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. Copper(I) Iodide Promoted [3+2]-Cycloaddition/Oxidation to Construct Pyrrolo[2,1-a]isoquinolinoquinones from Naphthoquinones and Tetrahydroisoquinolines;Synlett;2022-01-03

2. A3B type unsymmetrical and amphiphilic phthalocyanines: Synthesis, characterization, thermal stability and aggregation studies;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2020-02

3. Dual-directional alkyne-terminated macrocycles: Enroute to non-aggregating molecular platforms;Organic Chemistry Frontiers;2019

4. Arylhydrazone ligands as Cu-protectors and -catalysis promoters in the azide–alkyne cycloaddition reaction;Dalton Transactions;2019

5. Diaminodiacid-based synthesis of macrocyclic peptides using 1,2,3-triazole bridges as disulfide bond mimetics;RSC Advances;2017

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