reference/33446749

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/33446749

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issn	1520-6904 0022-3263
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pageRange	1448-1452
publicationName	The Journal of Organic Chemistry
startingPage	1448
bibliographicCitation	Liu D, Gao Y, Wang X, Kelley JA, Burke TR. Enantioselective Synthesis of N^α-Fmoc Protected (2S,3R)-3-Phenylpipecolic Acid. A Constrained Phenylalanine Analogue Suitably Protected for Solid-Phase Peptide Synthesis. J. Org. Chem. 2002 Feb 08;67(5):1448–52. doi: 10.1021/jo010124+.
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date	2002-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/11871872 https://doi.org/10.1021/jo010124%2B
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Enantioselective Synthesis of Nα-Fmoc Protected (2S,3R)-3-Phenylpipecolic Acid. A Constrained Phenylalanine Analogue Suitably Protected for Solid-Phase Peptide Synthesis
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Total number of triples: 56.