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Volumn 12, Issue 14, 2010, Pages 3124-3127

Enantioselective synthesis of a diastereomer of iriomoteolide-1a. What is the correct structure of the natural product?

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; BIOLOGICAL PRODUCT; IRIOMOTEOLIDE 1A; IRIOMOTEOLIDE-1A; MACROLIDE;

EID: 77954558790     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1011423     Document Type: Article
Times cited : (25)

References (58)
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    • For a list of these total syntheses, see the Supporting Information of
    • For a list of these total syntheses, see the Supporting Information of Bates, R. H.; Shotwell, J. B.; Roush, W. R. Org. Lett. 2008, 10, 4343-4346
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    • See also the references cited in refs 5b and 6
    • See also the references cited in refs 5b and 6.
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    • For some examples, see
    • For some examples, see
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    • Part of this work has been presented at the 239th ACS National Meeting: Mar 21-25 San Francisco, CA; American Chemical Society: Washington, DC, 2010; ORGN-123
    • Part of this work has been presented at the 239th ACS National Meeting: Yang, J.; Fang, L.; Yang, F. Abstracts of Papers. 239th ACS National Meeting; Mar 21-25, 2010, San Francisco, CA; American Chemical Society: Washington, DC, 2010; ORGN-123.
    • (2010) Abstracts of Papers. 239th ACS National Meeting
    • Yang, J.1    Fang, L.2    Yang, F.3
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    • Advance Article, DOI: 10.1039/c0cc00915f
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    • March 21-25, San Francisco, CA; American Chemical Society: Washington, DC, 2010; ORGN-131
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    • 6 from the spectra provided in the Supporting Information of ref 4a. This also strongly supports a 2 E -alkenonic ester rather than the originally assigned 2 Z- isomer
    • 6 from the spectra provided in the Supporting Information of ref 4a. This also strongly supports a 2 E -alkenonic ester rather than the originally assigned 2 Z- isomer
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    • For two reviews of the Mitsunobu reaction, see
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    • For some reviews, see
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    • Preliminary studies using model substrates showed that the tertiary C14 hydroxy group had to be protected
    • Preliminary studies using model substrates showed that the tertiary C14 hydroxy group had to be protected.
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    • Unpublished results
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    • For two recent reviews for structural misassignment of natural products, see
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    • Williams and co-workers recently described a similar intramolecular Nozaki-Hiyama reductive cyclization of formate esters
    • Williams and co-workers recently described a similar intramolecular Nozaki-Hiyama reductive cyclization of formate esters: Williams, D. R.; Walsh, M. J.; Miller, N. A. J. Am. Chem. Soc. 2009, 131, 9038-9045
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.