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Volumn 132, Issue 28, 2010, Pages 9900-9907

Synthesis of the QRSTU domain of maitotoxin and its 85- epi - And 86- epi -diastereoisomers

Author keywords

[No Author keywords available]

Indexed keywords

BUILDING BLOCKES; D-RIBOSE; DIASTEREOISOMERS; ENOL ETHERS; METHYL GROUP; NATURAL PRODUCTS; NMR SPECTROSCOPIC ANALYSIS; RING CLOSING METATHESIS; RING SYSTEMS; SYNTHETIC STRATEGIES; TARGET MOLECULE;

EID: 77954638231     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja103708j     Document Type: Article
Times cited : (34)

References (63)
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  • 29
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    • Clark, J.S.1
  • 30
    • 0001263185 scopus 로고
    • For earlier methods using ring-closing metathesis to form enol ethers, see
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    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5426
    • Fu, G.C.1    Grubbs, R.H.2
  • 37
    • 24944578549 scopus 로고    scopus 로고
    • For recent work using the Takai-Utimoto reagent for the synthesis of polyethers, see: Majumder, U. and Rainier, J. D. Tetrahedron Lett. 2005, 46, 7209
    • For recent work using the Takai-Utimoto reagent for the synthesis of polyethers, see
    • (2005) Tetrahedron Lett. , vol.46 , pp. 7209
    • Majumder, U.1    Rainier, J.D.2
  • 48
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    • For an application of water-promoted epoxide-opening cascades toward total synthesis
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    • (2009) J. Am. Chem. Soc. , vol.131 , pp. 6383
    • Byers, J.A.1    Jamison, T.F.2
  • 49
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    • For an application of water-promoted epoxide-opening cascades toward total synthesis, see
    • For an application of water-promoted epoxide-opening cascades toward total synthesis, see: Van Dyke, A. R. and Jamison, T. F. Angew. Chem., Int. Ed. 2009, 48, 4430
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 4430
    • Van Dyke, A.R.1    Jamison, T.F.2
  • 55
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    • For an example of a similar isomerization, see
    • For an example of a similar isomerization, see: Crimmins, M. T., McDougall, P. J., and Ellis, J. M. Org. Lett. 2006, 8, 4079
    • (2006) Org. Lett. , vol.8 , pp. 4079
    • Crimmins, M.T.1    McDougall, P.J.2    Ellis, J.M.3
  • 60
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    • 4-promoted cyclization of dithioketals to form O, S -ketal oxepanes followed by an oxidation/methylation procedure that gives similar diastereoselectivities, see
    • 4-promoted cyclization of dithioketals to form O, S -ketal oxepanes followed by an oxidation/methylation procedure that gives similar diastereoselectivities, see: Torikai, K., Yari, H., Murata, M., and Oishi, T. Heterocycles 2006, 70, 161
    • (2006) Heterocycles , vol.70 , pp. 161
    • Torikai, K.1    Yari, H.2    Murata, M.3    Oishi, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.