ChemInform Abstract: An Efficient Approach to Asymmetric Synthesis of Dipeptide β-Turn Mimetics:...

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2001 amino acids, peptides amino acids, peptides U 0400 30 - 193 An Efficient Approach to Asymmetric Synthesis of Dipeptide β- Turn Mimetics: Indolizidinone Amino Acids. — Based on an asymmetric hydrogenation of the key intermediate (II), an efficient approach to enantiopure indolizidinone amino acid esters such as (IV) is developed. — (WANG, WEI; XIONG, CHIYI; HRUBY, VICTOR J.; Tetrahedron Lett. 42 (2001) 18, 3159-3161; Dep. Chem., Univ. Ariz., Tucson, AZ 85721, USA; EN) 1

Transcript of ChemInform Abstract: An Efficient Approach to Asymmetric Synthesis of Dipeptide β-Turn Mimetics:...

Page 1: ChemInform Abstract: An Efficient Approach to Asymmetric Synthesis of Dipeptide β-Turn Mimetics: Indolizidinone Amino Acids.

2001 amino acids, peptides

amino acids, peptidesU 0400

30 - 193An Efficient Approach to Asymmetric Synthesis of Dipeptide β-Turn Mimetics: Indolizidinone Amino Acids. — Based on anasymmetric hydrogenation of the key intermediate (II), an efficient approachto enantiopure indolizidinone amino acid esters such as (IV) is developed.— (WANG, WEI; XIONG, CHIYI; HRUBY, VICTOR J.; Tetrahedron Lett.42 (2001) 18, 3159-3161; Dep. Chem., Univ. Ariz., Tucson, AZ 85721, USA; EN)

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