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Volumn 76, Issue 15, 2011, Pages 6038-6047

Asymmetric strecker synthesis of α-arylglycines

Author keywords

[No Author keywords available]

Indexed keywords

AMINONITRILES; ASYMMETRIC SYNTHESIS; CHIRAL AUXILIARIES; DERIVATIZATIONS; DIASTEREOMERIC; ENANTIOPURE; ETHYLAMINE; METHYL ESTERS; NITRILE GROUPS; NMR SPECTROSCOPIC ANALYSIS; SODIUM CYANIDE; STRECKER REACTIONS; STRECKER SYNTHESIS; THREE-COMPONENT;

EID: 79961064173     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200528s     Document Type: Article
Times cited : (29)

References (114)
  • 10
    • 36849051865 scopus 로고    scopus 로고
    • For a comprehensive review on the asymmetric synthesis of α-amino acids, see:;, and references therein
    • For a comprehensive review on the asymmetric synthesis of α-amino acids, see: Nájera, C.; Sansano, J. M. Chem. Rev. 2007, 107, 4584-4671 and references therein
    • (2007) Chem. Rev. , vol.107 , pp. 4584-4671
    • Nájera, C.1    Sansano, J.M.2
  • 39
  • 53
    • 61349167157 scopus 로고    scopus 로고
    • There are a few examples of the use of acetone cyanohydrin and acetyl cyanide as more experimentally favourable nucleophiles in Strecker reactions to form α-aryl-aminonitriles; see
    • There are a few examples of the use of acetone cyanohydrin and acetyl cyanide as more experimentally favourable nucleophiles in Strecker reactions to form α-aryl-aminonitriles; see: Sipos, S.; Jablonkai, I. Tetrahedron Lett. 2009, 50, 1844-1846
    • (2009) Tetrahedron Lett. , vol.50 , pp. 1844-1846
    • Sipos, S.1    Jablonkai, I.2
  • 56
    • 0033516455 scopus 로고    scopus 로고
    • For a review into the use of 1-phenylethylamine as a chiral auxiliary, see
    • For a review into the use of 1-phenylethylamine as a chiral auxiliary, see: Juaristi, E.; León-Romo, J. L.; Reyes, A.; Escalante, J. Tetrahedron: Asymmetry 1999, 10, 2441-2495
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 2441-2495
    • Juaristi, E.1    León-Romo, J.L.2    Reyes, A.3    Escalante, J.4
  • 70
    • 0035939191 scopus 로고    scopus 로고
    • Warmuth has shown that (S)-1-phenylethylamine can be selectively removed by hydrogenolysis to form α,α-alkyl-aryl-amino acids; see
    • Warmuth has shown that (S)-1-phenylethylamine can be selectively removed by hydrogenolysis to form α,α-alkyl-aryl-amino acids; see: Warmuth, R.; Munsch, T. E.; Stalker, R. A.; Li, B.; Beatty, A. Tetrahedron 2001, 57, 6383-6397
    • (2001) Tetrahedron , vol.57 , pp. 6383-6397
    • Warmuth, R.1    Munsch, T.E.2    Stalker, R.A.3    Li, B.4    Beatty, A.5
  • 85
    • 33646826338 scopus 로고    scopus 로고
    • For our previous methodology on the asymmetric synthesis of α-amino acids, see
    • For our previous methodology on the asymmetric synthesis of α-amino acids, see: Taylor, P. J. M.; Bull, S. D. Tetrahedron: Asymmetry 2006, 17, 1170-1178
    • (2006) Tetrahedron: Asymmetry , vol.17 , pp. 1170-1178
    • Taylor, P.J.M.1    Bull, S.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.