Invertomers at nitrogen in aziridine carboxylates by multinuclear (H-1, C-13, O-17 and N-15) NMR study

被引：0
|
作者：
Forni, A
Moretti, I
Mucci, A
Prati, F
Schenetti, L
机构：
来源：
KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII | 1995年 / 09期
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中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A configurational and conformational study of N-unsubstituted. N-acetyl- and N-sulfonylaziridine carboxylates has been performed by H-1, C-13, O-17 and N-15 NMR spectroscopy. The presence of acetyl and sulfonyl groups on the ring nitrogen atom seems to reduce greatly the configurational stability at nitrogen.
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页码：1226 / 1234
页数：9
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