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Data · collection · 2015

Efficient Synthesis of 3- R -Boc-amino-4-(2,4,5-trifluorophenyl)butyric Acid

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3- R -Boc-amino-4-(2,4,5-trifluorophenyl)butyric acid ( 9 ) was obtained from L -methionine in six steps with a total yield of 32%.

Description

The α-amino acid segment of L -methionine was transferred to chiral aziridine by amino protection, reduction, hydroxyl derivation, and cyclization. After ring opening of 2,4,5-trifluoro-phenyl magnesium bromide, the methylthiomethyl group was then hydrolyzed to β-amino alcohol and oxidized to the target β-amino acid.

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Provenance · 2 source records, 17 field assertions
SourceKeyLast seenRaw
DataCite10.6084/m9.figshare.c.206078011 d agoJSON v1
DataCite10.6084/m9.figshare.c.2060780.v111 d agoJSON v1
FieldAssertionExtractorEvidence
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concepts[field].local:field:physicsmapping · DataCitevocabulary-mapper@1.0.0keywords['Physics']
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