Issue 25, 2013
From the journal:

RSC Advances

The Baylis–Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes†

Deevi Basavaiah,*a   Katta Santosh Kumar,a   Kunche Aravindua  and  Balthu Lingaiaha  

* Corresponding authors

a School of Chemistry, University of Hyderabad, Hyderabad, India
E-mail: dbsc@uohyd.ernet.in
Fax: +91 40-23012460

Abstract

A general synthetic protocol for obtaining functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes containing 13-, 14-, 15-, 16- and 20-membered rings has been developed using Baylis–Hillman (BH) acetates as starting materials and ring closing metathesis as a key step.

Graphical abstract: The Baylis–Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes

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Article information

DOI
https://doi.org/10.1039/C3RA40926K
Article type
Communication
Submitted
22 Feb 2013
Accepted
23 Apr 2013
First published
23 Apr 2013

RSC Adv., 2013,3, 9629-9632

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The Baylis–Hillman acetates in organic synthesis: development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes

D. Basavaiah, K. S. Kumar, K. Aravindu and B. Lingaiah, RSC Adv., 2013, 3, 9629 DOI: 10.1039/C3RA40926K

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