eprintid: 19981
rev_number: 22
userid: 1419
dir: disk0/00/01/99/81
datestamp: 2013-11-12 17:17:27
lastmod: 2021-06-12 22:55:54
status_changed: 2013-11-12 17:17:27
type: article
metadata_visibility: show
item_issues_count: 0
eprint_status: archive
creators_name: Moss, RA
creators_name: Fu, X
creators_name: Tian, J
creators_name: Sauers, R
creators_name: Wipf, P
creators_email:
creators_email:
creators_email:
creators_email:
creators_email: pwipf@pitt.edu
creators_id:
creators_id:
creators_id:
creators_id:
creators_id: PWIPF
title: Stereochemistry of oxachlorocarbene SNi reactions
ispublished: pub
divisions: sch_as_chemistry
full_text_status: public
abstract: (Chemical Equation Presented) 3-Nortricyclyloxychlorocarbene and trans-4-methylcyclohexyloxychlorocarbene both fragment in hydrocarbon solvents with extensive loss of stereochemical integrity to the corresponding chlorides via competitive and nearly isoenergetic SNi-like transition states. © 2005 American Chemical Society.
date: 2005-03-31
date_type: published
publication: Organic Letters
volume: 7
number: 7
pagerange: 1371 - 1374
refereed: TRUE
issn: 1523-7060
id_number: 10.1021/ol050185k
pmid: 15787509
citation: Moss, RA and Fu, X and Tian, J and Sauers, R and Wipf, P (2005) Stereochemistry of oxachlorocarbene SNi reactions. Organic Letters, 7 (7). 1371 - 1374. ISSN 1523-7060
document_url: http://d-scholarship-dev.library.pitt.edu/19981/1/licence.txt