DocumentCode
445704
Title
Ring closing metathesis in the synthesis of sultones
Author
Karsch, Sandra ; Metz, Peter
Author_Institution
Institut of Org. Chem., Dresden Univ. of Technol., Germany
Volume
2
fYear
2004
fDate
26 June-3 July 2004
Firstpage
39
Abstract
Unsatured sultones with normal, medium and large ring sizes were efficiently synthesized by ring closing metathesis (RCM) of sulfonates. The resulting α,β-unsaturated sultones act as dienophils in intermolecular Diels-Alder reactions. A first cyclic sulfate formation through RCM has been discovered.
Keywords
catalysis; organic compounds; reaction kinetics; α,β-unsaturated sultones; cyclic sulfate formation; dienophils; intermolecular Diels-Alder reactions; ring closing metathesis; Chemical technology; Chemistry; Nitrogen;
fLanguage
English
Publisher
ieee
Conference_Titel
Science and Technology, 2004. KORUS 2004. Proceedings. The 8th Russian-Korean International Symposium on
Print_ISBN
0-7803-8383-4
Type
conf
DOI
10.1109/KORUS.2004.1555531
Filename
1555531
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