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

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Kumar, Katta Santosh
dc.contributor.author Aravindu, Kunche
dc.contributor.author Lingaiah, Balthu
dc.date.accessioned 2022-03-27T09:01:08Z
dc.date.available 2022-03-27T09:01:08Z
dc.date.issued 2013-07-07
dc.description.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. © 2013 The Royal Society of Chemistry.
dc.identifier.citation RSC Advances. v.3(25)
dc.identifier.uri 10.1039/c3ra40926k
dc.identifier.uri http://xlink.rsc.org/?DOI=c3ra40926k
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12275
dc.title The Baylis-Hillman acetates in organic synthesis: Development of a facile strategy for synthesis of functionalized unsaturated benzo-fused macrocyclic ethers and [n] metacyclophanes
dc.type Journal. Article
dspace.entity.type
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