FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes.
Chem Commun (Camb). 2013 Sep 21; 49(73):8051-3.CC

Abstract

Highly substituted indene derivatives were readily prepared in excellent yields with high regioselectivity under very mild reaction conditions by the FeCl3 mediated intramolecular olefin-cationic cyclization of cinnamates.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Dethe DH

Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur 208016, India. ddethe@iitk.ac.in

Murhade GM

No affiliation info available

MeSH

AlkenesCationsCinnamatesCyclizationIndenesMolecular StructureStereoisomerism

Pub Type(s)

Journal Article

Language

eng

PubMed ID

23902996

Citation

Dethe, Dattatraya H., and Ganesh M. Murhade. "FeCl3 Mediated Intramolecular Olefin-cation Cyclization of Cinnamates for the Synthesis of Highly Substituted Indenes." Chemical Communications (Cambridge, England), vol. 49, no. 73, 2013, pp. 8051-3.

Dethe DH, Murhade GM. FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes. Chem Commun (Camb). 2013;49(73):8051-3.

Dethe, D. H., & Murhade, G. M. (2013). FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes. Chemical Communications (Cambridge, England), 49(73), 8051-3. https://doi.org/10.1039/c3cc43159b

Dethe DH, Murhade GM. FeCl3 Mediated Intramolecular Olefin-cation Cyclization of Cinnamates for the Synthesis of Highly Substituted Indenes. Chem Commun (Camb). 2013 Sep 21;49(73):8051-3. PubMed PMID: 23902996.

* Article titles in AMA citation format should be in sentence-case

TY - JOUR T1 - FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes. AU - Dethe,Dattatraya H, AU - Murhade,Ganesh M, Y1 - 2013/08/01/ PY - 2013/8/2/entrez PY - 2013/8/2/pubmed PY - 2014/3/13/medline SP - 8051 EP - 3 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) VL - 49 IS - 73 N2 - Highly substituted indene derivatives were readily prepared in excellent yields with high regioselectivity under very mild reaction conditions by the FeCl3 mediated intramolecular olefin-cationic cyclization of cinnamates. SN - 1364-548X UR - https://www.unboundmedicine.com/medline/citation/23902996/FeCl3_mediated_intramolecular_olefin_cation_cyclization_of_cinnamates_for_the_synthesis_of_highly_substituted_indenes_ L2 - https://doi.org/10.1039/c3cc43159b DB - PRIME DP - Unbound Medicine ER -

Tags

FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes.Chem Commun (Camb). 2013 Sep 21; 49(73):8051-3.CC