A facile and novel method for the synthesis of 2-isoxazolines
β Scribed by Raekyu Chang; Kyongtae Kim
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 247 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Treatment of allylic esters such as allyl benzoate (3a), allyl phenylacetate (4), allyl 3-phenylpropanoate (5), crotyl esters 14, 4-bromo-2-butenyl esters 15, and 1,4-bis(aroyloxy)-2-butenes 16 with NOBF4 in CH3CN at -23Β°C gave alkanoyloxy (or aroyloxy)-2-isoxazolines and 3-substituted 4-alkanoyloxy (or aroyloxy)-2-isoxazolines, depending on the allylic esters.
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A one pot, high yield synthesis of depsipeptides is described involving room temperature condensation of hindered substrates (N-BOC amino acids and benzyl cc-hydroxy esters) in the presence of DCC and a dialkylaminopyridine. lo. 40 5. M. M.
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A simple synthesis of the 3(2H)-furanone ring system is described. The 3(2H)-furanone moeity is a central structural unit in a growing number of natural products including simple compounds such as bullatenone and geiparvarin and more complex compounds such as jatrophone, the eremantholides, and lyc
## Abstract magnified image Triarylpyrylium perchlorates are readily and selectively converted into corresponding 2βisoxazolines in good yield and short reaction time using solventless conditions. J. Heterocyclic Chem., (2009).