[2.2.2.2](2,7)‐1‐Bromonaphthalenophane from a Desymmetrized Building Block Bearing Electrophilic and Masked Nucleophilic Functionalities-Reference-Cited by-同舟云学术

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[2.2.2.2](2,7)‐1‐Bromonaphthalenophane from a Desymmetrized Building Block Bearing Electrophilic and Masked Nucleophilic Functionalities

Published:2019-02-26 Issue:3 Volume:102 Page:e1800242
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Cai Guangke¹,Chatterjee Shreyam²^ORCID,Hisaki Ichiro³^ORCID,Tobe Yoshito¹²⁴^ORCID

Affiliation:

1. Division of Frontier Materials Science, Graduate School of Engineering ScienceOsaka University, Toyonaka 560-8531 Osaka Japan

2. Nanoscience and Nanotechnology Center, The Institute of Scientific and Industrial ResearchOsaka University, Ibaraki 567-0047 Osaka Japan

3. Research Institute for Electronic ScienceHokkaido University Sapporo 001-0020 Japan

4. Department of Applied ChemistryNational Chiao Tung University 1001 Ta Hsueh Road Hsinchu 30010 Taiwan

Funder

JSPS KAKENHI

Nanotechnology Platform at Nara Institute of Science and Technology

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hlca.201800242

Reference32 articles.

1. D. J. Cram ‘Preorganization–From Solvents to Spherands’ Angew. Chem. Int. Ed.1986 25 1039–1057.

2. I. Tabushi K. Yamamura ‘Cyclophanes 1’ in ‘Topics in Current Chemistry’ Vol. 113 Ed. F. Vögtle Springer-Verlag 1983 p. 145.

3. K. Odashima K. Koga in ‘Cyclophanes’ Vol. 2 Eds. P. M. Keehn S. M. Rosenfeld Academic Press New York 1983 p. 483.

4. F. Diederich ‘Complexation of Neutral Molecules by Cyclophane Hosts’ Angew. Chem. Int. Ed.1988 27 362–386.

5. F. Diederich ‘Cyclophanes’ The Royal Society of Chemistry Cambridge 1991.

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1. The Versatile and Strategic O-Carbamate Directed Metalation Group in the Synthesis of Aromatic Molecules: An Update;Chemical Reviews;2024-06-12

2. Directed Ortho and Remote Metalation of Naphthalene 1,8-Diamide: Complementing SEAr Reactivity for the Synthesis of Substituted Naphthalenes;Organic Letters;2021-03-05

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