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Volumn 45, Issue 19, 2004, Pages 3707-3712

Synthetic studies on thiostrepton family of peptide antibiotics: Synthesis of the pentapeptide segment containing dihydroxyisoleucine, thiazoline and dehydroamino acid

Author keywords

Dihydroxyisoleucine; Sulfinimines; Thiazolines; Thioamides; Thiostrepton

Indexed keywords

CARBOXYLIC ACID; DEHYDROAMINO ACID; DIHYDROQUINOLINE DERIVATIVE; DIHYDROXYISOLEUCINE; IMINE; LACTONE; OXAZOLINE DERIVATIVE; PENTAPEPTIDE; PIPERIDINE DERIVATIVE; POLYPEPTIDE ANTIBIOTIC AGENT; SULFINIMINE; TETRAHYDROPYRIDINE; THIAZOLINE; THIOSTREPTON; UNCLASSIFIED DRUG; VINYLZINC; ZINC DERIVATIVE;

EID: 1842861694     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.03.099     Document Type: Article
Times cited : (34)

References (78)
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    • note
    • Recently, construction of thiostrepton analogs with the thiazoline-containing macrocycle by the conceptually different route has been appeared; see Ref. [4d].
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    • Synthesis of the β-substituted β-phenylselenoamino acids by the different route, see Ref. [7d]. See also:
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    • note
    • Reaction temperature for both the transmetallation and addition steps was crucial to yield and diastereoselectivity.
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    • note
    • 25-4.4 ( c 1, 1 M AcOH)].
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    • note
    • 1H NMR spectrum was different from that of 25.
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    • note
    • Because of susceptibility of the thiazoline ring, we suspect that the epimerization occurred at the C4-position of the thiazoline ring.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.