Efficient synthesis of (2R,3S)-2-amino-3-(benzyloxy)-4,4,4-trifluorobutanoic acid (4,4,4-trifluoro-OBn-d-allothreonine)-Reference-Cited by-同舟云学术

Efficient synthesis of (2R,3S)-2-amino-3-(benzyloxy)-4,4,4-trifluorobutanoic acid (4,4,4-trifluoro-OBn-d-allothreonine)

Published:2010-10 Issue:41 Volume:51 Page:5361-5363
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Zeng Chun-min,Kerrigan Sean A.,Katzenellenbogen John A.,Slocum Connie,Gallacher Kyla,Shomali Maysoun,Lyttle C. Richard,Hattersley Gary,Miller Chris P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. The Many Roles for Fluorine in Medicinal Chemistry

2. Fluorine in Pharmaceuticals: Looking Beyond Intuition

3. Stereocontrolled synthesis of 4,4,4-trifluorothreonine

4. Addition of Chiral Glycine, Methionine, and Vinylglycine Enolate Derivatives to Aldehydes and Ketones in the Preparation of Enantiomerically Pure ?-Amino-?-Hydroxy Acids

5. General method for the synthesis of enantiomerically pure β-hydroxy-α-amino acids, containing fluorine atoms in the side chains. Case of stereochemical distinction between methyl and trifluoromethyl groups. X-Ray crystal and molecular structure of the nickel(II) complex of (2S,3S)-2(trifluoromethyl)threonine

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