An enantioselective, stereodivergent approach to anti- and syn-α-hydroxy-β-amino acids from anti-3-amino-1,2-diols. Synthesis of the ready for coupling taxotere® side chain.-Reference-Cited by-同舟云学术

An enantioselective, stereodivergent approach to anti- and syn-α-hydroxy-β-amino acids from anti-3-amino-1,2-diols. Synthesis of the ready for coupling taxotere® side chain.

Published:1996-01 Issue:1 Volume:7 Page:243-262
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Pastó Mireia,Moyano Albert,Pericàs Miquel A.,Riera Antoni

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference59 articles.

1. Tributyltin Cyanide, a Novel Reagent for the Stereoselective Preparation of 3-Amino-2-hydroxy Acids via Cyanohydrin Intermediates

2. Synthesis of .beta.-amino-.alpha.-hydroxy acids via aldol condensation of a chiral glycolate enolate. A synthesis of (-)-bestatin

3. Design and synthesis of an orally potent human renin inhibitor containing a novel amino acid, cyclohexylnorstatine

4. A stereoselective synthesis of cyclohexylnorstatine, the key component of a renin inhibitor

5. Synthesis of the ketodifluoromethylene dipeptide isostere

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