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Convenient Synthesis of N ‐Terminal Tfm‐Dipeptides from Unprotected Enantiopure α‐Tfm‐Proline and α‐Tfm‐Alanine (Eur. J. Org. Chem. 33/2009)
Author(s) -
Chaume Grégory,
Lensen Nathalie,
Caupène Caroline,
Brigaud Thierry
Publication year - 2009
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.200990093
Subject(s) - enantiopure drug , chemistry , alanine , proline , dipeptide , stereochemistry , amino acid , organic chemistry , enantioselective synthesis , biochemistry , catalysis
The cover picture shows that enantiopure fluorinated amino acids and peptides are conveniently obtained from ethyl trifluoropyruvate and trifluoroacetone. Details are discussed in the article by T. Brigaud et. al. on p. 5717 ff. The background is a picture of the Zen garden of the Tôfuku‐ji temple in Kyoto.