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Synlett

Volumn , Issue 16, 2008, Pages 2437-2442

Synthesis and reactivity of novel α,α,β- and α,α,δ-trichlorinated imines

(3) D'Hooghe, Matthias a De Meulenaer, Bruno a De Kimpe, Norbert a

a GHENT UNIVERSITY (Belgium)

Author keywords

2 (chloromethyl) aziridines; Hydride reagents; Trichlorinated imines; Trichloroamines

Indexed keywords

AZIRIDINE DERIVATIVE; IMINE; METHANOL; NITRILE; NITROGEN; OXYGEN; SULFUR;

ADDITION REACTION; ARTICLE; CHEMICAL STRUCTURE; CHLORINATION; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS;

EID: 54149107257 PISSN: 09365214 EISSN: None Source Type: Journal
DOI: 10.1055/s-2008-1078171 Document Type: Article

Times cited : (10)

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46
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47
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58
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- 3N: C, 35.23; H, 5.91; N, 6.85. Found: C, 35.11; H, 6.09; N, 6.74; for chlorine isotopes, the reported relative intensity (%) represents the largest peak.
- 3N: C, 35.23; H, 5.91; N, 6.85. Found: C, 35.11; H, 6.09; N, 6.74; for chlorine isotopes, the reported relative intensity (%) represents the largest peak.

59
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60
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- +], 57 (100), 56 (3); for chlorine isotopes, the reported relative intensity (%) represents the largest peak.
- +], 57 (100), 56 (3); for chlorine isotopes, the reported relative intensity (%) represents the largest peak.

61
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64
- 54149113087
- 3N: C, 41.31; H, 6.93; N, 6.02. Found: C, 41.47; H, 7.13; N, 5.92; for chlorine isotopes, the reported relative intensity (%) represents the largest peak.
- 3N: C, 41.31; H, 6.93; N, 6.02. Found: C, 41.47; H, 7.13; N, 5.92; for chlorine isotopes, the reported relative intensity (%) represents the largest peak.

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