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Volumn 128, Issue 19, 2006, Pages 6304-6305

Asymmetric synthesis of protected arylglycines by rhodium-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters

Author keywords

[No Author keywords available]

Indexed keywords

BORONIC ACID DERIVATIVE; ESTER DERIVATIVE; GLYCINE DERIVATIVE; N TERT BUTANESULFINYLIMINO ESTER DERIVATIVE; RHODIUM; UNCLASSIFIED DRUG;

EID: 33646590315     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja060529h     Document Type: Article
Times cited : (125)

References (26)
  • 8
    • 0001122927 scopus 로고
    • (e) For a review on asymmetric arylglycine syntheses, see: Williams, R. M.; Hendrix, J. A. Chem. Rev. 1992, 92, 889.
    • (1992) Chem. Rev. , vol.92 , pp. 889
    • Williams, R.M.1    Hendrix, J.A.2
  • 24
    • 0036828151 scopus 로고    scopus 로고
    • N-Sulfinyl β-amino acids have been employed in peptide coupling reactions, but racemization is not possible for these systems. Tang, T. P.; Ellman, J. A. J. Org. Chem. 2002, 67, 7819.
    • (2002) J. Org. Chem. , vol.67 , pp. 7819
    • Tang, T.P.1    Ellman, J.A.2
  • 26
    • 33646566213 scopus 로고    scopus 로고
    • note
    • Deprotection of the sulfinyl group from 9 with methanolic HCl proceeded in 93% yield (see Supporting Information).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.