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A useful route to (R)‐ and (S)‐ tert ‐leucine
Author(s) -
Allenmark Stig,
Lamm Bo
Publication year - 2000
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/1520-636x(2001)13:1<43::aid-chir9>3.0.co;2-g
Subject(s) - chemistry , leucine , chirality (physics) , enantiomer , stereochemistry , resolution (logic) , amino acid , biochemistry , chiral symmetry , artificial intelligence , physics , quantum mechanics , computer science , nambu–jona lasinio model , quark
Resolution of 1‐(2‐furyl)‐2,2‐dimethylpropylamine, an intermediate on a synthetic route to tert ‐leucine, followed by oxidation of the respective enantiomers, constitutes an interesting and useful strategy to (R)‐ and (S)‐ tert ‐leucine. Chirality 13:43–47, 2001. © 2000 Wiley‐Liss, Inc.