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Volumn 16, Issue 7, 2011, Pages 5422-5436

Synthesis of key fragments of amphidinolide Q - A cytotoxic 12-membered macrolide

Author keywords

Amphidinium sp.; Amphidinolide Q; Cytotoxic marine natural product; Macrolide synthesis

Indexed keywords

AMPHIDINOLIDE Q; ASCORBIC ACID; MACROLIDE;

EID: 79960758197     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules16075422     Document Type: Article
Times cited : (6)

References (10)
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    • Radha Krishna, P.; Narsingam, M. Studies directed towards the stereoselective total synthesis of ilexlactone via a tandem ring-closing enyne metathesis protocol. Tetrahedron Lett. 2007, 48, 8721-8724. (Pubitemid 350054959)
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    • Radha Krishna, P.1    Narsingam, M.2
  • 6
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    • Use of ?-allyltricarbonyliron lactone complexes in the synthesis of taurospongin A: A potent inhibitor of DNA polymerase β and HIV reverse transcriptase
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    • A short approach to the bicyclo[4.3.0]nonane fragment of stawamycin
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    • An efficient and enantioselective total synthesis of naturally occurring L-783277
    • Choi, H.G.; Son, J.B.; Park, D.; Ham, Y.J.; Hah, J.; Sim, T. An efficient and enantioselective total synthesis of naturally occurring L-783277. Tetrahedron Lett. 2010, 51, 4942-4946.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.