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Volumn 8, Issue 8, 2006, Pages 1705-1708

Solid-phase synthesis of succinylhydroxamate peptides: Functionalized matrix metalloproteinase inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

ADAM PROTEIN; ENZYME INHIBITOR; FLUORESCENT DYE; HYDROXAMIC ACID; METALLOPROTEINASE; PEPTIDE; SUCCINIC ACID DERIVATIVE;

EID: 33646462137     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol060409e     Document Type: Article
Times cited : (23)

References (23)
  • 13
    • 32644481005 scopus 로고    scopus 로고
    • During the preparation of this manuscript, a paper appeared reporting the synthesis of a library of diastereomeric inhibitors with R = H by using an alternative, racemic building block with O-trityl protection: Wang, J.; Uttamchandani, M.; Sun, L. P.; Yao, S. Q. Chem. Commun. 2006, 717-719.
    • (2006) Chem. Commun. , pp. 717-719
    • Wang, J.1    Uttamchandani, M.2    Sun, L.P.3    Yao, S.Q.4
  • 14
    • 0034641457 scopus 로고    scopus 로고
    • For selected examples of hydroxamate solution syntheses from carboxylic acids, see: (a) Reddy, A. S.; Kumar, M. S.; Reddy, G. R. Tetrahedron Lett. 2000, 41, 6285-6288.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 6285-6288
    • Reddy, A.S.1    Kumar, M.S.2    Reddy, G.R.3
  • 20
    • 33646464781 scopus 로고    scopus 로고
    • note
    • 2EtN resulted in complete consumption of 7a but also substantial side reactions.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.