@article{8fb970d3effa40559cbf230d515401de,
title = "2-(2,3-Dihydro-1H-indol-3-yl)ethanol: synthesis, separation of enantiomers, and assignment of absolute stereochemistry by X-ray structure analysis",
abstract = "The first direct resolution of racemic 2-(2,3-dihydro-lH-indol-3-yl)ethanol-prepared by catalytic hydrogenation of 2-(lH-indol-3-yl)ethanol-has been accomplished by chiral simulated moving bed (SMB) chromatography. The single enantiomers were isolated as their dihydrogen phosphate salts. Single-crystal X-ray analyses were successful, revealing that the (+)-enantiomer of 2-(2,3-dihydro-lH-indol-3-yl)ethanol has the (S) configuration. Chirality 16:126-130, 2004.",
keywords = "Chromatography, High Pressure Liquid, Crystallography, X-Ray, Ethanol, Hydrogen, Indoles, Ligands, Models, Molecular, Molecular Conformation, Molecular Structure, Phosphates, Receptors, Dopamine D2, Receptors, Dopamine D4, Stereoisomerism",
author = "Frydenvang, {Karla Andrea} and Sommer, {Michael Bech} and Dieter Heckmann and Ole Nielsen and Benny Bang-Andersen",
note = "Copyright 2004 Wiley-Liss, Inc.",
year = "2004",
doi = "10.1002/chir.10313",
language = "English",
volume = "16",
pages = "126--30",
journal = "Chirality",
issn = "0899-0042",
publisher = "Wiley",
number = "2",
}