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
Norbert De Kimpe, Matthias D’hooghe, Study of the ring opening of 2-(alkanoyloxymethyl)aziridinium salts by bromide and fluoride: change in regioselectivity, in Proceedings of The 10th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2006, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-10-01377
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Study of the ring opening of 2-(alkanoyloxymethyl)aziridinium salts by bromide and fluoride: change in regioselectivity

Norbert De Kimpe 1
1. Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium
Abstract
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Keywords
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N,N-Dimethylthiosemicarbazones of Acetylpyrazines: Preparation and Their Hydrophobic Properties
Asymmetric aza-Diels-Alder reaction of Danishefsky’s diene with imines in a chiral reaction medium