Concise Synthesis of All Stereoisomers of b-Methoxytyrosine and Determination of the Absolute Configuration of the Residue in Callipeltin A

Zampella, A.; D'Orsi, R.; Sepe, V.; Casapullo, Agostino; Monti, Maria Chiara; D'Auria, M. V.

doi:10.1021/ol0513600

All stereoisomers of â-methoxytyrosine (â-OMeTyr), a stereo-undefined component of callipeltin A, were synthesized from L- and D-tyrosine. The stereochemistry of â-OMeTyr in callipeltin A was determined to be 2R,3R by an oxidative procedure and Marfey’s analysis.

Titolo:	Concise Synthesis of All Stereoisomers of b-Methoxytyrosine and Determination of the Absolute Configuration of the Residue in Callipeltin A
Autori:	ZAMPELLA A. D'ORSI R. SEPE V. CASAPULLO, Agostino MONTI, Maria Chiara D'AURIA M. V. mostra contributor esterni nascondi contributor esterni
Data di pubblicazione:	2005
Rivista:	ORGANIC LETTERS
Abstract:	All stereoisomers of â-methoxytyrosine (â-OMeTyr), a stereo-undefined component of callipeltin A, were synthesized from L- and D-tyrosine. The stereochemistry of â-OMeTyr in callipeltin A was determined to be 2R,3R by an oxidative procedure and Marfey’s analysis.
Handle:	http://hdl.handle.net/11386/1059048
Appare nelle tipologie:	1.1.2 Articolo su rivista con ISSN

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