2004
DOI: 10.1016/j.tet.2003.11.056
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Stereoselective synthesis of heterosubstituted aziridines and their functionalization

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Cited by 38 publications
(25 citation statements)
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“…Imines were prepared starting from the corresponding carbonyl compounds and amines. [46] The allylic halides 10f, 10i and 10l were prepared starting from commercially available 1-butene, 2-hexene and 1-hexene, respectively, by bromination with N-bromosuccinimide. Petroleum ether refers to the fraction boiling in the range 40Ϫ60°C.…”
Section: Methodsmentioning
confidence: 99%
“…Imines were prepared starting from the corresponding carbonyl compounds and amines. [46] The allylic halides 10f, 10i and 10l were prepared starting from commercially available 1-butene, 2-hexene and 1-hexene, respectively, by bromination with N-bromosuccinimide. Petroleum ether refers to the fraction boiling in the range 40Ϫ60°C.…”
Section: Methodsmentioning
confidence: 99%
“…Based on data reported in the literature for trifluoromethyl aziridines 97 and bidiaziridines, 98 the absolute configuration of the obtained compounds was deduced from 2D-NOESY correlations performed on purified (R,S,S)-140 and (R,R,R)-140'. While no NOE interaction was observed in the minor isomer, a significant NOE interaction between (CH 3 ) 3 −C and H bound to trifluoromethyl substituted carbon was detected in the major isomer, suggesting a 2S,3S absolute configuration for the diaziridine ring of the latter.…”
Section: Scheme 64 Synthesis Of Trifluoromethyl Diaziridinesmentioning
confidence: 99%
“…d¼À72.5 (d, 3 d¼0.99 (s, 9H, major), 1.00 (s, 9H, minor), 1.07 (d, 3 J¼6. 9 Hz, 3H, minor), 1.21 (d, 3 J¼6. 4 Hz, 3H, major), 1.87e1.98 (m, 2H), 4.09 (q, 3 J HeF ¼3.…”
Section: General Procedures For the Synthesis Of 2-alkyl-3-(trifluorommentioning
confidence: 99%