102210-03-7Relevant articles and documents
Solvent-controlled asymmetric strecker reaction: Stereoselective synthesis of α-trifluoromethylated α-amino acids
Wang, Hua,Zhao, Xiaoming,Li, Youhua,Lu, Long
, p. 1379 - 1381 (2007/10/03)
Stereoselective approaches to α-trifluoromethylated α-amino acids (α-Tim AAs) have been developed. The stereoconfigurations of the resulting α-Tfm AA precursors were well controlled by using different solvents. The optically active (S)-2-amino-2-phenyl-1,
Synthesis of nonracemic α-trifluoromethyl α-amino acids from sulfinimines of trifluoropyruvate
Asensio, Amparo,Bravo, Pierfrancesco,Crucianelli, Marcello,Farina, Alessandra,Fustero, Santos,Soler, Juan García,Meille, Stefano V.,Panzeri, Walter,Viani, Fiorenza,Volonterio, Alessandro,Zanda, Matteo
, p. 1449 - 1458 (2007/10/03)
We describe a novel and useful method for the synthesis of nonracemic α-trifluoromethyl α-amino acids (α-Tfm-AAs). Key building blocks are the sulfinimines (S)-1a and (S)-1b, prepared by Staudinger reaction from trifluoropyruvate esters and the chiral N-sulfinyl iminophosphorane (S)-8, which were treated with benzyl, allyl, and alkylmagnesium halides. The resulting diastereomeric N-sulfinyl α-Tfm α-amino esters, 12 and 13, were produced with moderate to good stereoselectivity and yields. When alkyl Grignard reagents were used, stereocontrol became progressively higher with increasing steric bulk, while reversed, though poor, stereocontrol was achieved with benzyl/allyl Grignard reagents. An explanation for the observed stereochemical outcome is proposed, on the basis of the exclusive E geometry (N-sulfinyl and CF3 trans about the C=N bond) of the chiral sulfinimines 1. This assignment is the product of structural correlation and is supported by ab initio calculations and NOE experiments. Sulfinamides 12 and 13 were transformed into a series of nonracemic α-Tfm-AAs 16-22. The sulfinyl auxiliary can be regenerated and recycled.
Sulfinimines of trifluoropyruvate: Novel intermediates for chiral non racemic α-trifluoromethyl α-amino acids
Bravo, Pierfrancesco,Crucianelli, Marcello,Vergani, Barbara,Zanda, Matteo
, p. 7771 - 7774 (2007/10/03)
A new and preparatively useful method for the synthesis of non racemic α-trifluoromethyl (Tfm)α-amino acids (AAs) is presented. Key-building blocks are the sulfinimines (S)-1a,b, prepared via Staudinger reaction from trifluoropyruvic esters and the chiral N-sulfinyl iminophosphorane (S)-5, which were reacted with benzyl and alkylmagnesium halides. The resulting N- sulfinyl α-Tfm α-amino esters 6a,b and 6c-g, respectively, were produced with opposite stereoselectivity. The stereocontrol with alkyl Grignard reagents was progressively higher with increasing steric bulk. Some of the adducts 6 were transformed into a-Tfm-phenylalanine (R)-8 (with regeneration and recycling the chiral auxiliary), αTfm-leucine (S)-11c, α-Tfm-butyrine (S)-11f and α-Tfm-alanine (8),11g in two steps in one-pot.
