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Volumn 75, Issue 4, 2010, Pages 1293-1296

Synthesis of the conformationally constrained tyrosine analogues, (R)- and (S)-5-hydroxy-2-aminoindan-2-carboxylic acids

(3) Murigi, Francis N a Nichol, Gary S a Mash, Eugene A a

a University of Arizona (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABSOLUTE CONFIGURATION; CHEMICAL EQUATIONS; CHROMATOGRAPHIC SEPARATIONS; DIASTEREOMERIC; DIPEPTIDE DERIVATIVES; L-PHENYLALANINE; TYROSINE ANALOGUES; X-RAY CRYSTALLOGRAPHIC ANALYSIS;

CARBOXYLIC ACIDS; CHEMICAL REACTIONS; LIQUID CHROMATOGRAPHY; ORGANIC ACIDS; PHOSPHATASES;

AMINO ACIDS;

AMINE; CARBOXYLIC ACID DERIVATIVE; DIPEPTIDE DERIVATIVE; HYDROXYL GROUP; INDAN DERIVATIVE; PHENYLALANINE DERIVATIVE; TYROSINE DERIVATIVE;

ARTICLE; COLUMN CHROMATOGRAPHY; CONFORMATION; DIASTEREOISOMER; QUANTUM YIELD; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

CHROMATOGRAPHY, GEL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CRYSTALLOGRAPHY, X-RAY; DIPEPTIDES; INDANS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR CONFORMATION; MOLECULAR STRUCTURE; PHENYLALANINE; STEREOISOMERISM; TYROSINE;

EID: 77249126422 PISSN: 00223263 EISSN: 15206904 Source Type: Journal
DOI: 10.1021/jo902438s Document Type: Article

Times cited : (9)

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- Crystal data for (R,S)-8: C29H 30BrN3O4S; M, 596.53 g mol -1, T, 100(2) K, Cu Kα, thin colorless plates, orthorhombic, P212121, a, 10.2029(2, b, 10.3818(2, c, 25.7025(4) Å, α, 90°, β, 90°, γ, 90°, V=2722.52(9)A ° 3,Z=4, 5021 reflections,Rint 0.0567,GOFon F2=1.196, R1, 0.0433 and wR2, 0.1011, F2 > 2σ, R1, 0.0463 and wR2, 0.1024 all data
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- Hydrogenolysis of bromide 9 affords a convenient method for introduction of an isotopic label into the resolved amino acid.

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