Stereoselective synthesis of 3-heteroaromatic-substituted alanines

Tetrahedron Asymmetry

Volumn 11, Issue 12, 2000, Pages 2635-2642

  Croce, Piero Dalla ^a   La Rosa, Concetta ^b   Pizzatti, Enrica ^a  

^a Dipartimento di Chimica Organica e Industriale   (Italy)

^b Facolta di Farmacia   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

2,5 DIHYDRO 3,6 DIMETHOXY 2 ISOPROPYLPYRAZINE; ALANINE DERIVATIVE; HETEROCYCLIC COMPOUND; REAGENT; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; CHEMICAL REACTION; CONTROLLED STUDY; DIASTEREOISOMER; DRUG CONFORMATION; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROLYSIS; MODEL; OPTICAL ROTATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

EID: 0034733612     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)00223-8     Document Type: Article

References (7)

1. Barret, G. C. Chemistry and Biochemistry of the Amino Acids; Chapman and Hall: London, 1985.
2. Coppola, G. M.; Schuster, H. F. Asymmetric Synthesis: Construction of Chiral Molecules using Aminoacids; John Wiley & Sons: New York, 1987.
3. Meiwes, J.; Schudok, M.; Kretzschmar, G. Tetrahedron: Asymmetry 1997, 8, 527-536.
4. Bozell, J. J.; Vogt, C. E.; Gozum, J. J. Org. Chem. 1991, 56, 2584-2587.
5. Döbler, C.; Kreuzfeld, H. J.; Michalik, M.; Krause, H. W. Tetrahedron: Asymmetry 1996, 7, 117-125.
6. Schöllkopf, U. Tetrahedron 1983, 39, 2085-2091.
7. 20=+7.55 (c 1 in EtOH).