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Volumn 64, Issue 7, 1999, Pages 2174-2175

Novel synthesis of α-amino acid derivatives through triethylborane- induced solid-phase radical reactions

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID DERIVATIVE;

EID: 0033515460     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo982466u     Document Type: Article
Times cited : (51)

References (49)
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    • (b) Chem. Rev. 1997, 97(2), 347-510.
    • (1997) Chem. Rev. , vol.97 , Issue.2 , pp. 347-510
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    • (g) Acc. Chem. Res. 1996, 29(3), 112-170.
    • (1996) Acc. Chem. Res. , vol.29 , Issue.3 , pp. 112-170
  • 19
    • 7044286458 scopus 로고    scopus 로고
    • (d) Snider, B. B. Chem. Rev. 1996, 96, 339. For selected examples, see:
    • (1996) Chem. Rev. , vol.96 , pp. 339
    • Snider, B.B.1
  • 32
    • 0032568895 scopus 로고    scopus 로고
    • Oxime ethers are well-known to be excellent radical acceptors because of the extra stabilization of the intermediate aminyl radical provided by the adjacent oxygen atom. See: (a) Miyabe, H.; Torieda, M.; Inoue, K.; Tajiri, K.; Kiguchi, T.; Naito, T. J. Org. Chem. 1998, 63, 4397.
    • (1998) J. Org. Chem. , vol.63 , pp. 4397
    • Miyabe, H.1    Torieda, M.2    Inoue, K.3    Tajiri, K.4    Kiguchi, T.5    Naito, T.6
  • 44
    • 0345539858 scopus 로고    scopus 로고
    • note
    • Wang and TentaGel OH resins purchased from Novabiochem were used in all experiments.
  • 45
    • 0001422153 scopus 로고
    • 2CC=NOBn) was readily prepared from O-benzyloxyamine hydrochloride and glyoxylic acid monohydrate. See the Supporting Information and also see: Kolasa, T.; Sharma, S. K.; Miller, M. J. Tetrahedron 1988, 44, 5431.
    • (1988) Tetrahedron , vol.44 , pp. 5431
    • Kolasa, T.1    Sharma, S.K.2    Miller, M.J.3
  • 46
    • 0345539857 scopus 로고    scopus 로고
    • note
    • 13C NMR, and HRMS.
  • 48
    • 0345539856 scopus 로고    scopus 로고
    • note
    • Glyoxylic imines are convenient starting materials for the synthesis of α-amino acids through ene reactions, cycloadditions, or the nucleophilic additions of organometallic reagents or enolate anion equivalents.
  • 49
    • 0344246062 scopus 로고    scopus 로고
    • note
    • All reactions were run in commercially available solvents and with reagents without requiring any special precautions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.