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Volumn 33, Issue 22, 2003, Pages 3913-3917

Synthesis and Structure Determination of (2S, 2′ S)-3-Phenyl-2-(pyrrolidin-2′-yl)-propionic Acid

Author keywords

2, 3 Homoproline derivative; (2S, 2 S) 3 Phenyl 2 (pyrrolidin 2 yl)propionic acid; (4S, 4aS) 4 Benzyl 4a, 5,6,7 tetrahydro pyrrolo 1,2 c pyrimidine 1,3 dione; Synthesis

Indexed keywords

3 PHENYL 2 (PYRROLIDIN 2' YL)PROPIONIC ACID; 4 BENZYL 4A,5,6,7 TETRAHYDROPYRROLO[1,2 C]PYRIMIDINE 1,3 DIONE; PROLINE; PROPIONIC ACID DERIVATIVE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0344413581     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120026314     Document Type: Article
Times cited : (3)

References (14)
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    • Cheng, R.P.1    Gellman, S.H.2    DeGrado, W.F.3
  • 2
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    • For reviews, see: Cole, D.C. Recent stereoselective synthetic approaches to β-amino acids. Tetrahedron 1994, 50, 9517.
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  • 3
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    • 3-Homoproline: what are the secondary sturctures of β-peptides lacking H-bonds? Helv. Chim. Acta 1999, 82, 1539.
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  • 4
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    • Synthesis of the enantiomeric 2-pyrrolidineacetic acids
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    • Cassal, J.M.1    Fuerst, A.2    Meier, W.3
  • 5
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    • Synthesis of α-L-homoproline and derivatives. Preparation of 7-α-L-homoprolinebradykinin
    • (b) Balaspiri, L.; Penke, B.; Papp, G.; Dombi, G.; Kovacs, K. Synthesis of α-L-homoproline and derivatives. Preparation of 7-α -L-homoprolinebradykinin. Helv. Chim. Acta 1975, 58, 969;
    • (1975) Helv. Chim. Acta , vol.58 , pp. 969
    • Balaspiri, L.1    Penke, B.2    Papp, G.3    Dombi, G.4    Kovacs, K.5
  • 6
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    • Contribution to the asymmetric synthesis of bicyclic compounds catalyzed by optically active amino acids. Synthesis of (S)-2-pyrrolidinepropionic acid and (R)-4-amino-5-phenylvaleric acid
    • (c) Buchschacher, P.; Cassal, J.M.; Fuerst, A.; Meier, W.; Contribution to the asymmetric synthesis of bicyclic compounds catalyzed by optically active amino acids. Synthesis of (S)-2-pyrrolidinepropionic acid and (R)-4-amino-5-phenylvaleric acid. Helv. Chim. Acta 1977, 60, 2747.
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  • 7
    • 0345492501 scopus 로고    scopus 로고
    • note
    • 4: C, 71.37; H, 6.56; N, 3.96. Found: C, 71.19; H, 6.49; N, 4.05. For both two compounds, the existence of rotator is observed in their NMR spectra.
  • 8
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    • note
    • 2: C, 71.21; H, 7.81; N, 6.39. Found: C, 70.87; H, 7.81; N, 6.45.
  • 9
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    • note
    • 2; 244.1212. Found: 244.1212.
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    • note
    • b supported the (4S, 4aS) configuration of 4.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.