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Volumn 44, Issue 6, 2003, Pages 1235-1238

Efficient synthesis of optically active α-substituted glutamate analogs possessing α-hydroxymethyl and α-alkoxymethyl groups

Author keywords

substituted glutamate analogs; Asymmetric Strecker synthesis; Etherification; mGluRs agonist; Protection; Sterically hindered amine

Indexed keywords

ALPHA (HYDROXYMETHYL)GLUTAMATE; ALPHA BENZYLOXYMETHYL DERIVATIVE; ALPHA HYDROXYMETHYL DERIVATIVE; GLUTAMATE RECEPTOR; GLUTAMIC ACID DERIVATIVE; METABOTROPIC RECEPTOR AGONIST; UNCLASSIFIED DRUG;

EID: 0037415466     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)02810-1     Document Type: Article
Times cited : (20)

References (27)
  • 1
    • 0024829451 scopus 로고
    • Parthasarathy
    • Collingridge G.L., Lester R.A. Pharmacol. Rev. 40:1989;143-210 Parthasarathy, H. S., Ed. Neurological disorders. Nature 1999, 399 (Suppl.), A1-A47.
    • (1989) Pharmacol. Rev. , vol.40 , pp. 143-210
    • Collingridge, G.L.1    Lester, R.A.2
  • 18
    • 0012827397 scopus 로고    scopus 로고
    • L-Valine was a superior acyloxy group to other amino acids in the present substrate. The use of L-phenylalanine gave a 10:1 mixture of (5S)- and (5R)-α-amino nitrile in 60% yield.
    • L-Valine was a superior acyloxy group to other amino acids in the present substrate. The use of L-phenylalanine gave a 10:1 mixture of (5S)- and (5R)-α-amino nitrile in 60% yield.
  • 19
    • 0012880420 scopus 로고    scopus 로고
    • An intermediary cyclic imine was isolated in a small amount, presumably, because of elimination of HCN from the products.
    • An intermediary cyclic imine was isolated in a small amount, presumably, because of elimination of HCN from the products.
  • 21
    • 0012779429 scopus 로고    scopus 로고
    • 8
    • 8.
  • 23
    • 0012767889 scopus 로고    scopus 로고
    • 4NOH for the Boc protection of sterically hindered amines will be reported, separately.
    • 4NOH for the Boc protection of sterically hindered amines will be reported, separately.
  • 27
    • 0012780898 scopus 로고    scopus 로고
    • note
    • 2O): δ 181.4, 174.6, 162.1, 138.2, 129.2, 74.1, 72.9, 65.5, 32.4, 29.6.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.