eprintid: 19879
rev_number: 12
userid: 1418
dir: disk0/00/01/98/79
datestamp: 2013-10-18 17:33:41
lastmod: 2017-10-13 20:56:27
status_changed: 2013-10-18 17:33:41
type: article
metadata_visibility: show
item_issues_count: 0
eprint_status: archive
creators_name: Shin, Y
creators_name: Fournier, JH
creators_name: Fukui, Y
creators_name: Brückner, AM
creators_name: Curran, DP
creators_email: 
creators_email: 
creators_email: 
creators_email: 
creators_email: curran@pitt.edu
creators_id: 
creators_id: 
creators_id: 
creators_id: 
creators_id: CURRAN
title: Total synthesis of (-)-dictyostatin: Confirmation of relative and absolute configurations
ispublished: pub
divisions: sch_as_chemistry
full_text_status: public
abstract: Will the real dictyostatin please stand up? There were five finalists as stereostructures for the potent anticancer agent dictyostatin; ten, if one were to include enantiomers. A total synthesis of (-)-dictyostatin (1) has ended the decade-old masquerade and identified the winner as a structure recently proposed by Paterson and Wright.
date: 2004-09-06
date_type: published
publication: Angewandte Chemie - International Edition
volume: 43
number: 35
pagerange: 4634 - 4637
refereed: TRUE
issn: 1433-7851
id_number: 10.1002/anie.200460593
pmid: 15316999
mesh_headings: Macrolides--chemical synthesis
mesh_headings: Macrolides--chemistry
mesh_headings: Molecular Conformation
chemical_names: Macrolides
chemical_names: dictyostatin
citation:   Shin, Y and Fournier, JH and Fukui, Y and Brückner, AM and Curran, DP  (2004) Total synthesis of (-)-dictyostatin: Confirmation of relative and absolute configurations.  Angewandte Chemie - International Edition, 43 (35).  4634 - 4637.  ISSN 1433-7851     
document_url: http://d-scholarship-dev.library.pitt.edu/19879/1/licence.txt