Synthèse et réactivité des halogéno-2 sulfonyl-2 aziridines
1979 ◽
Vol 57
(15)
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pp. 1958-1966
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Carbon tetrahalide reacts rapidly with 2-phenylsulfonyl aziridines in the presence of KOH, leading to 2-phenylsulfonyl 2-haloaziridines.Starting with 2-isopropylsulfonyl aziridines, a monochloro and a dichloroaziridine are produced; the Ramberg–Bäcklund reaction is not observed.These halo compounds decompose either thermally or in acidic medium leading to N-substituted α-haloacetamides and α-phenylsulfonylacetamides. 2-Phenylsulfonyl 2-haloaziridines are unreactive toward potassium cyanide or sodium thiophenoxide. Sodium methoxide, sodium ethoxide, or sodium thioethoxide reduce them to 2-phenylsulfonyl aziridines; the reaction depends upon the solvent.
Keyword(s):
1980 ◽
Vol 94
(2)
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pp. 361-367
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Keyword(s):
2014 ◽
Vol 1033-1034
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pp. 76-80
1929 ◽
Vol 48
(6)
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pp. 589-592
2012 ◽
Vol 1009
◽
pp. 42-48
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2011 ◽
Vol 17
(1)
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pp. 91-97
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Keyword(s):
1990 ◽
Vol 48
(3)
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pp. 448-449