N,N′-transphthaloylation in a monoprotected diamine

Synthesis

Volumn , Issue 6, 2006, Pages 983-988

  McCormick, Joan E ^a   McElhinney, R Stanley ^a   McMurry, T Brian H ^a   O'Brien, John E ^a  

^a TRINITY COLLEGE DUBLIN   (Ireland)

Author keywords

Hindered amines; N phthaloyl protecting groups; NMR spectra; Restricted rotation; Transphthaloylation

Indexed keywords

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ROTATION; THERMAL EFFECTS;

HINDERED AMINES; N-PHTHALOYL PROTECTING GROUPS; NMR SPECTRA; RESTRICTED ROTATION; TRANSPHTHALOYLATION;

AMINES;

3 (2 PHTHALIMIDOETHOXY) 3 (5 FLUOROURACIL 1 YL)PROPYLAMINE; ACID ANHYDRIDE; DIAMINE DERIVATIVE; HYDRAZIDE DERIVATIVE; N [2 [3 AMINO 1 (5 FLUOROURACIL 1 YL)PROPOXY]ETHYL] N',N' DIISOPROPYLPHTHALAMIDE; N [3 [2 (DIISOPROPYLAMIDOCARBONYLBENZAMIDO)ETHOXY] 3 (5 FLUOROURACIL 1 YL)PROPYL]PHTHALIMIDE; N BENZYL N',N' DIISOPROPYLPHTHALAMIDE; N BENZYL O (1 PYRROLIDINYLCARBONYL)BENZAMIDE; PHTHALIMIDE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL BOND; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ROOM TEMPERATURE;

EID: 33645340854     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926362     Document Type: Article

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