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Volumn 16, Issue 47, 2010, Pages 14083-14093

Total syntheses of the thiopeptides smythiamicin C and D

Author keywords

antibiotics; cross coupling; macrocycles; natural products; total synthesis

Indexed keywords

AMIDE BOND FORMATION; BITHIAZOLE; CROSS COUPLING REACTIONS; CROSS-COUPLINGS; DIASTEREOSELECTIVE ADDITIONS; MACROCYCLES; MAGNESIUM BROMIDE; NATURAL PRODUCTS; NEGISHI CROSS-COUPLING; REGIO-SELECTIVE; REGIOSELECTIVE METALATION; RING CLOSURES; STILLE CROSS-COUPLING; SYNTHETIC SEQUENCE; TARGET COMPOUND; TITLE COMPOUNDS; TOTAL SYNTHESIS; TRISUBSTITUTED PYRIDINES;

EID: 78650292242     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201002144     Document Type: Article
Times cited : (28)

References (103)
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    • Further key synthetic work in the area
    • Further key synthetic work in the area
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    • note
    • The specific rotation determined for compound 8 with 88 % ee was [α] ${{{20\hfill \atop {\rm D}\hfill}}}$ =-26.7 (c=1.0 in MeOH). A literature reference [6b] provides for the same compound a specific rotation of [α] ${{{20\hfill \atop {\rm D}\hfill}}}$ =-25.7 (c=1.01 in MeOH).
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    • For a review on the synthesis of polyazoles related to natural products
    • For a review on the synthesis of polyazoles related to natural products, see:, E. Riego, D. Hernández, F. Albericio, M. Ólvarez, Synthesis 2005, 1907-1922.
    • (2005) Synthesis , pp. 1907-1922
    • Riego, E.1    Hernández, D.2    Albericio, F.3    Ólvarez, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.