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Volumn 61, Issue 8, 2008, Pages 615-629

Solution-phase peptide synthesis; Synthesis of 'North-Western' and 'South Eastern' fragments of the antifungal cyclodepsipeptide petriellin A

Author keywords

[No Author keywords available]

Indexed keywords

ANTI-FUNGAL; CYCLIC DEPSIPEPTIDE; HEPTAMER; HEXAMER; PEPTIDE SYNTHESIS; SOLUTION-PHASE SYNTHESIS;

EID: 49749139769     PISSN: 00049425     EISSN: None     Source Type: Journal    
DOI: 10.1071/CH08132     Document Type: Article
Times cited : (4)

References (28)
  • 9
    • 39049107344 scopus 로고    scopus 로고
    • A. B. Hughes, B. E. Sleebs, Aust. J. J. Chem. 2008, 61, 131.
    • A. B. Hughes, B. E. Sleebs, Aust. J. J. Chem. 2008, 61, 131.
  • 11
    • 33745802361 scopus 로고    scopus 로고
    • L. Aurelio, R. T. C. Brownlee, J. Dang, J. B. Gloer, A. B. Hughes G. M. Polya, Aust. J. Chem. 2006, 59, 407. doi:10.1071/CH06148
    • L. Aurelio, R. T. C. Brownlee, J. Dang, J. B. Gloer, A. B. Hughes G. M. Polya, Aust. J. Chem. 2006, 59, 407. doi:10.1071/CH06148
  • 13
    • 49749133141 scopus 로고    scopus 로고
    • Compounds 9, 13, and 55 were commercial products.
    • Compounds 9, 13, and 55 were commercial products.
  • 14
    • 49749140056 scopus 로고    scopus 로고
    • 3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 10.
    • 3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 10.
  • 15
    • 0026783997 scopus 로고    scopus 로고
    • Compound 12 was prepared from racemic pipecolinic acid by resolution via tartrate salts (D. S. Perlow, J. M. Erb, N. P. Gould, R. D. Tung, R. M. Freidinger, P. D. Williams, D. F. Veber, J. Org. Chem. 1992, 57, 4394).
    • Compound 12 was prepared from racemic pipecolinic acid by resolution via tartrate salts (D. S. Perlow, J. M. Erb, N. P. Gould, R. D. Tung, R. M. Freidinger, P. D. Williams, D. F. Veber, J. Org. Chem. 1992, 57, 4394).
  • 16
    • 84988088747 scopus 로고    scopus 로고
    • The resolved salt was then carbamoylated E. Ponnusamy, U. Fotadar, A. Spisni, D. Fiat, Synthesis 1986, 48;
    • The resolved salt was then carbamoylated (E. Ponnusamy, U. Fotadar, A. Spisni, D. Fiat, Synthesis 1986, 48;
  • 17
    • 49749115184 scopus 로고    scopus 로고
    • 3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 12.
    • 3, BnBr, DMF) followed by treatment with HCl(g) in ether to give the hydrochloride 12.
  • 18
    • 0001023731 scopus 로고
    • Compound 15 was identical to material described by
    • Compound 15 was identical to material described by J. R. McDermott, N. L. Benoiton, Can. J. Chem. 1973, 51, 1915.
    • (1973) Can. J. Chem , vol.51 , pp. 1915
    • McDermott, J.R.1    Benoiton, N.L.2
  • 19
    • 0001001070 scopus 로고
    • Compound 17 was identical to material described by
    • Compound 17 was identical to material described by S. T. Cheung, N. L. Benoiton, Can. J. Chem. 1977, 55, 906.
    • (1977) Can. J. Chem , vol.55 , pp. 906
    • Cheung, S.T.1    Benoiton, N.L.2
  • 24
    • 49749113207 scopus 로고    scopus 로고
    • Although Scheme 8 depicts the Z-dehydro compound 58, no attempt was made to determine the double bond configuration
    • Although Scheme 8 depicts the Z-dehydro compound 58, no attempt was made to determine the double bond configuration.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.