Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/13017
Title: Reactivity of a-Oxophosphonium Ylides: A Contribution to the Mechanistics
Authors: Melo, Teresa M. Pinho e 
Gonsalves, António M. d'A. Rocha 
Carrapato, Sara M. 
Taborda, Ana M. 
Keywords: Phosphorus ylides; Tetrasubstituted alkenes
Issue Date: 1999
Publisher: Molecular Diversity Preservation International
Citation: Molecules. 4:7 (1999) 219-231
Serial title, monograph or event: Molecules
Issue: 4:7
Abstract: Ylides 1f and 1g react with chlorine, with bromine and with N-chlorosuccinimide in the presence of a range of nucleophiles. The 2,3-disubstitutedbutenedioates obtained in this way allow us to gather more information about the mechanism involved. Ylide 1c was also studied showing similar reactivity and leading to the highly selective synthesis of 2,3- disubstituted-3-phenylpropenoates
URI: https://hdl.handle.net/10316/13017
ISSN: 1420-3049
DOI: 10.3390/40700219
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

Files in This Item:
File Description SizeFormat
Reactivity of a-Oxophosphonium Ylides.pdf48.02 kBAdobe PDFView/Open
Show full item record

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.