EventsThe 10th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 10th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2006
Citation
Ewan Boyd, Jason Eames, Alastair Hay, Ray H.V. Jones, Rachel Stenson, Michael J. Suggate, Enantioselective Protonation of Prostereogenic Enol Equivalents, in Proceedings of The 10th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2006, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-10-01388
Share
Email
Facebook
Twitter
LinkedIn

Enantioselective Protonation of Prostereogenic Enol Equivalents

Ewan Boyd 1
Jason Eames 2
Alastair Hay 1
Ray H.V. Jones 1
Rachel Stenson 3
Michael J. Suggate 4
1. Syngenta, Grangemouth Manufacturing Centre, Earls Road, Grangemouth, Scotland, FX3 8XG
2. Department of Chemistry, University of Hull, Kingston upon Hull, HU6 7RX
3. Syngenta, Global Specialist Technology, PO Box A38, Leeds Road, Huddersfield, UK, HD2 1FF
4. Department of Chemistry, Queen Mary, University of London, Mile End Road, London, UK E1 4NS
Abstract
n/a
Keywords
n/a
An Expeditious Synthesis of N-Functionalized Isoindolinones. Application to the Synthesis of Biologically Active Compounds
Synthesis and Reactions of 5-Hydroxy-pyrido[3,2,1-jk]carbazol-4,6-diones