Improved Synthesis of Larger Resorcinarenes-Reference-Cited by-同舟云学术

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Improved Synthesis of Larger Resorcinarenes

Published:2016-06-17 Issue:13 Volume:81 Page:5726-5731
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Della Sala Paolo¹,Gaeta Carmine¹,Navarra Wanda¹,Talotta Carmen¹,De Rosa Margherita¹,Brancatelli Giovanna²,Geremia Silvano²,Capitelli Francesco³,Neri Placido¹

Affiliation:

1. Dipartimento di Chimica e Biologia, Università di Salerno, Via Giovanni Paolo II 132, I-84084 Fisciano (Salerno), Italy

2. Centro di Eccellenza in Biocristallografia, Dipartimento di scienze Chimiche e Farmaceutiche, Università di Trieste, via L. Giorgieri 1, 34127 Trieste, Italy

3. Istituto di Cristallografia-CNR, Via Salaria Km 29.300, 00015 Monterotondo (Roma), Italy

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b00803

Reference38 articles.

1. Calixarenes and Beyond

2. para-Bridged Symmetrical Pillar[5]arenes: Their Lewis Acid Catalyzed Synthesis and Host–Guest Property

3. Biphen[n]arenes

4. Calixnaphthalenes: Deep, Electron-Rich Naphthalene Ring-Containing Calixarenes. The First Decade.

5. Synthesis, Structure, and[60]Fullerene Complexation Properties of Azacalix[m]arene[n]pyridines

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1. Deep-Cavity Calix[4]naphth[4]arene Macrocycles: Synthesis, Conformational Features, and Solid-State Structures;Molecules;2024-08-31

2. Quinoacridane[4]arenes─Very Large Conformationally Restricted Macrocycles;Organic Letters;2024-07-25

3. Friedel–Crafts Acylation for Accessing Multi‐Bridge‐Functionalized Large Pillar[n]arenes;Angewandte Chemie International Edition;2024-01-08

4. Friedel–Crafts Acylation for Accessing Multi‐Bridge‐Functionalized Large Pillar[n]arenes;Angewandte Chemie;2024-01-08

5. State-of-the-art and recent progress in resorcinarene-based cavitand;Chinese Chemical Letters;2023-10

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