Stereoselective synthesis of stable isotope-labeled L-α-amino acids: ELectrophilic amination of Oppolzer's acyl sultams in the synthesis of L-[15N]alanine, L-[15N]valine, L-[15N]leucine, L-[15N]phenylalanine and L-[1-13C, 15N]valine

Journal of Labelled Compounds and Radiopharmaceuticals

Volumn 38, Issue 3, 1996, Pages 238-248

  Lodwig, Siegfried N ^b   Unkefer, Clifford J ^a  

^a LOS ALAMOS NATIONAL LABORATORY   (United States)

^b Centralia College   (United States)

Author keywords

1 chloro 1 15n nitrosocyclohexane; Bornane 10,2 sultam; Camphor 10 2 sultam; L 15n alanine; L 15n leucine; L 15n phenylalanine l 1 13c,15n valine; L 15n valine

Indexed keywords

AMINES; II-VI SEMICONDUCTORS; ISOTOPES; STEREOSELECTIVITY; ZINC OXIDE;

1-CHLORO-1-[15N]NITROSOCYCLOHEXANE; AMINO-ACIDS; BORNANE-10,2-SULTAM; CAMPHOR-10-2-SULTAM; L-[15N]ALANINE; L-[15N]LEUCINE; L-[15N]PHENYLALANINE L-[1-13C,15N]VALINE; L-[15N]VALINE; SULTAMS;

AMINO ACIDS;

DRYOBALANOPS;

ALANINE; AMINO ACID; CARBON 13; LEUCINE; NITROGEN 15; PHENYLALANINE; VALINE;

AMINO ACID SYNTHESIS; ARTICLE; CONTROLLED STUDY; ISOTOPE LABELING;

EID: 0029997388     PISSN: 03624803     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1099-1344(199603)38:3<239::aid-jlcr831>3.0.co;2-e     Document Type: Article

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