eprintid: 19542
rev_number: 16
userid: 1418
dir: disk0/00/01/95/42
datestamp: 2013-08-07 15:09:07
lastmod: 2019-02-02 15:58:26
status_changed: 2013-08-07 15:09:07
type: article
metadata_visibility: show
item_issues_count: 0
eprint_status: archive
creators_name: González-López De Turiso, F
creators_name: Curran, DP
creators_email: 
creators_email: curran@pitt.edu
creators_id: 
creators_id: CURRAN
title: Radical cyclization approach to spirocyclohexadienones
ispublished: pub
divisions: sch_as_chemistry
full_text_status: public
abstract: (Chemical Equation Presented) Cyclization of an aryl radical at the ipso position of a p-O-aryl-substituted acetamide or benzamide generates oxindoles or quinolones bearing spirocyclohexadienone rings. This versatile reaction is applied to formal syntheses of the vasopressin inhibitor SR121463A and aza-galanthamine.
date: 2005-01-06
date_type: published
publication: Organic Letters
volume: 7
number: 1
pagerange: 151 - 154
refereed: TRUE
issn: 1523-7060
id_number: 10.1021/ol0477226
pmid: 15625000
mesh_headings: Cyclization
mesh_headings: Cyclohexanes--chemistry
mesh_headings: Cyclohexenes
mesh_headings: Spiro Compounds--chemistry
chemical_names: Cyclohexanes
chemical_names: Cyclohexenes
chemical_names: Spiro Compounds
chemical_names: cyclohexadienone
citation:   González-López De Turiso, F and Curran, DP  (2005) Radical cyclization approach to spirocyclohexadienones.  Organic Letters, 7 (1).  151 - 154.  ISSN 1523-7060     
document_url: http://d-scholarship-dev.library.pitt.edu/19542/1/licence.txt