eprintid: 17269
rev_number: 26
userid: 1418
dir: disk0/00/01/72/69
datestamp: 2013-02-08 20:58:22
lastmod: 2021-09-07 23:55:02
status_changed: 2013-02-08 20:58:22
type: article
metadata_visibility: show
item_issues_count: 0
eprint_status: archive
creators_name: Bruch, A
creators_name: Ambrosius, A
creators_name: Fröhlich, R
creators_name: Studer, A
creators_name: Guthrie, DB
creators_name: Zhang, H
creators_name: Curran, DP
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creators_email: curran@pitt.edu
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creators_id: CURRAN
title: Memory of axial chirality in aryl radical phosphanylations
ispublished: pub
divisions: sch_as_chemistry
full_text_status: public
abstract: The rate constant for phosphanylation of an aryl radical with trimethylstannyl diphenylphosphane (Me3SnPPh2) has been measured as kphos ≈ 9 × 108 M-1 s -1. Aryl radicals derived from several axially chiral o-haloanilides are trapped by Me3SnPPh2 with complete retention of axial chirality as shown by oxidation of the phosphanes to give stable, easily analyzed phosphane oxides or sulfides. Double phosphanylations of o,o′-dihaloanilides followed by treatment with H2O2 or S8 in either order give enantiomers of a mixed diphosphane oxide sulfide. Chemodivergent trapping of diastereomers of an N-(cyclohex-2-enyl) anilide anilide is observed. For one isomer, the cyclization precedes the Me3SnPPh2 trapping, while for the other isomer direct trapping with Me3SnPPh2 supersedes the cyclization. The products are chiral triaryl phosphanes, oxides, and sulfides that are potentially interesting ligands in asymmetric catalysis. © 2010 American Chemical Society.
date: 2010-08-25
date_type: published
publication: Journal of the American Chemical Society
volume: 132
number: 33
pagerange: 11452 - 11454
refereed: TRUE
issn: 0002-7863
id_number: 10.1021/ja105070k
pmid: 20666512
citation:   Bruch, A and Ambrosius, A and Fröhlich, R and Studer, A and Guthrie, DB and Zhang, H and Curran, DP  (2010) Memory of axial chirality in aryl radical phosphanylations.  Journal of the American Chemical Society, 132 (33).  11452 - 11454.  ISSN 0002-7863     
document_url: http://d-scholarship-dev.library.pitt.edu/17269/1/licence.txt