Expedient Synthesis of C3-Symmetric Hexasubstituted Benzenes via Nicholas Reaction/[2 + 2 + 2] Cycloaddition. New Platforms for Molecular Recognition-Reference-Cited by-同舟云学术

Expedient Synthesis of C3-Symmetric Hexasubstituted Benzenes via Nicholas Reaction/[2 + 2 + 2] Cycloaddition. New Platforms for Molecular Recognition

Published:2013-12-23 Issue:2 Volume:16 Page:552-555
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Carrillo Romen¹,Martín Tomás²¹,López-Rodríguez Matías¹,Pinacho Crisóstomo Fernando²

Affiliation:

1. Instituto Universitario de Bio-Orgánica “Antonio González”, Universidad de La Laguna (ULL), Avda. Francisco Sánchez 2, 38206 La Laguna, Tenerife, Spain

2. Instituto de Productos Naturales y Agrobiología, Consejo Superior de Investigaciones Científicas (CSIC), Avda. Francisco Sánchez 3, 38206 La Laguna, Tenerife, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol403428p

Reference22 articles.

1. Inherently chiral concave molecules—from synthesis to applications

2. Benzocyclotrimers: From the Mills−Nixon Effect to Gas Hosting

3. Gas Hosting in Enantiopure Self-Assembled Oximes

4. A NovelC3-Symmetric Triol as Chiral Receptor for Ammonium Ions

5. Rational Design and Gas-Phase Characterization of Molecular Capsules by Self-Assembly of a Symmetric Hexasubstituted Benzene with Seven-Membered Lactams

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