One-step conversions of a simple corrole into chiral and amphiphilic derivatives

Tetrahedron Letters

Volumn 44, Issue 30, 2003, Pages 5669-5673

  Saltsman, Irena ^a   Goldberg, Israel ^b   Gross, Zeev ^a  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

5,10,15 TRIS(PENTAFLUOROPHENYL)CORROLE; AMPHOPHILE; BENZENE DERIVATIVE; GALLIUM; MACROCYCLIC COMPOUND; PHOSGENE; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CHEMICAL REACTION; CHIRALITY; CRYSTAL STRUCTURE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; X RAY CRYSTALLOGRAPHY;

EID: 0038505303     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01356-X     Document Type: Article

References (53)

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47. -.
48. 14.
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50. 3 (near the partly disordered dichloromethane solvent). The N-pyrrole proton was located in residual electron-density maps. CCDC 210816.
51. --COOH].
52. -.
53. 3. The carboxyl proton was located on a difference-Fourier map. The carboxyl group is not involved in H-bonding due to a sterically hindered environment. CCDC 210815.