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Volumn 39, Issue 3, 2009, Pages 523-530

Efficient large-scale synthesis of Boc-L-azatyrosine

Author keywords

Hydroxy deboronation; Large scale; Negishi cross coupling

Indexed keywords

METHYL 3 (5 HYDROXYPYRIDIN 2 YL) 2 [(2 METHYLPROPAN 2 YL)OXYCARBONYLAMINO]PROPANOATE; TERT BUTYLOXYCARBONYLAZATYROSINE; TYROSINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 61649108409     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910802406695     Document Type: Article
Times cited : (3)

References (11)
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  • 5
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    • Enantioselective synthesis of (2-pyridyl)alanines via catalytic hydrogenation and application to the synthesis of L-azatyrosine
    • Adamczyk, M.; Akireddy, S. R.; Reddy, R. E. Enantioselective synthesis of (2-pyridyl)alanines via catalytic hydrogenation and application to the synthesis of L-azatyrosine. Org. Lett. 2001, 20, 3157-3159.
    • (2001) Org. Lett , vol.20 , pp. 3157-3159
    • Adamczyk, M.1    Akireddy, S.R.2    Reddy, R.E.3
  • 6
    • 0010527612 scopus 로고    scopus 로고
    • Preparation of Nα-Boc 4-O-diethylphospho-L-azatyrosine, a reagent potentially useful for the synthesis of signal transduction related peptides
    • Ye, B.; Otaka, B.; Burke Jr., T. R. Preparation of Nα-Boc 4-O-diethylphospho-L-azatyrosine, a reagent potentially useful for the synthesis of signal transduction related peptides. Synlett 1996, 459-460.
    • (1996) Synlett , pp. 459-460
    • Ye, B.1    Otaka, B.2    Burke Jr., T.R.3
  • 7
    • 36849051865 scopus 로고    scopus 로고
    • For a recent review covering all the recent advances in the area of catalytic α amino acid synthesis, see Nàjera, C, Sansano, J. M. Catalytic asymmetric synthesis of α-amino acids. Chem. Rev. 2007, 117, 4584-4671
    • For a recent review covering all the recent advances in the area of catalytic α amino acid synthesis, see Nàjera, C.; Sansano, J. M. Catalytic asymmetric synthesis of α-amino acids. Chem. Rev. 2007, 117, 4584-4671.
  • 8
    • 0026708781 scopus 로고
    • Preparation of enantiomerically pure protected 4-oxo α-amino acids and 3-aryl α-amino acids from serine
    • Jackson, R. F. W.; Wishart, N.; Wood, A.; James, K.; Wythes, M. J. Preparation of enantiomerically pure protected 4-oxo α-amino acids and 3-aryl α-amino acids from serine. J. Org. Chem. 1992, 57, 3397-3404.
    • (1992) J. Org. Chem , vol.57 , pp. 3397-3404
    • Jackson, R.F.W.1    Wishart, N.2    Wood, A.3    James, K.4    Wythes, M.J.5
  • 9
    • 0348252422 scopus 로고    scopus 로고
    • Preparation of enantiomerically pure pyridyl amino acids from serine
    • Tabanella, S.; Valancogne, I.; Jackson, R. F. W. Preparation of enantiomerically pure pyridyl amino acids from serine. Org. Biomol. Chem. 2003, 1, 4254-4261.
    • (2003) Org. Biomol. Chem , vol.1 , pp. 4254-4261
    • Tabanella, S.1    Valancogne, I.2    Jackson, R.F.W.3
  • 10
    • 12344249722 scopus 로고    scopus 로고
    • Efficient synthesis of halohydroxypyridines by hydroxydeboronation
    • Voisin, A. S.; Bouillon, A.; Lancelot, J. C.; Rault, S. Efficient synthesis of halohydroxypyridines by hydroxydeboronation. Tetrahedron 2005, 61, 1417-1421.
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  • 11
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    • Boc-β-iodo-Ala-OMe can be readily obtained as a stable white solid from Boc-Ser-OMe in just one-step following the procedure described by Trost, B. M, Rudd, M. T. Chemoselectivity of the ruthenium-catalyzed hydrative diyne cyclization: Total synthesis of, -cylindricine C, D, and E. Org. Lett. 2003, 5, 4599-4602
    • Boc-β-iodo-Ala-OMe can be readily obtained as a stable white solid from Boc-Ser-OMe in just one-step following the procedure described by Trost, B. M.; Rudd, M. T. Chemoselectivity of the ruthenium-catalyzed hydrative diyne cyclization: Total synthesis of (+)-cylindricine C, D, and E. Org. Lett. 2003, 5, 4599-4602.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.