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Volumn 9, Issue 21, 2007, Pages 4303-4306

Synthesis of the ABCD trioxadispiroketal subunit of azaspiracid-1: An iodoetherification-dehydroiodination strategy for complex spiroketals

Author keywords

[No Author keywords available]

Indexed keywords

AZASPIRACID; FURAN DERIVATIVE; IODINATED HYDROCARBON; MARINE TOXIN; SPIRO COMPOUND; SPIROKETAL; UNCLASSIFIED DRUG;

EID: 35549001076     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol701866v     Document Type: Article
Times cited : (26)

References (54)
  • 8
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    • Nicolaou, K. C.; Frederick, M. O.; Petrovic, G.; Cole, K. P.; Loizidou, E. Z. Angew. Chem., Int. Ed. 2006, 45, 2609-2615.
    • (f) Nicolaou, K. C.; Frederick, M. O.; Petrovic, G.; Cole, K. P.; Loizidou, E. Z. Angew. Chem., Int. Ed. 2006, 45, 2609-2615.
  • 11
    • 34347231611 scopus 로고    scopus 로고
    • Angew. Chem., Int. Ed. 2007, 46, 4698-4703.
    • (2007) Angew. Chem., Int. Ed , vol.46 , pp. 4698-4703
  • 30
    • 33845185080 scopus 로고
    • For general reviews on spiroketal syntheses: a
    • For general reviews on spiroketal syntheses: (a) Perron, F.; Albizati, K. F. Chem. Rev. 1989, 89, 1617-1661.
    • (1989) Chem. Rev , vol.89 , pp. 1617-1661
    • Perron, F.1    Albizati, K.F.2
  • 36
    • 0036134411 scopus 로고    scopus 로고
    • Selected recent synthesis of complex spiroketals: (a) Hao, J.; Forsyth, C J. Tetrahedron Lett. 2002, 43, 1-2.
    • Selected recent synthesis of complex spiroketals: (a) Hao, J.; Forsyth, C J. Tetrahedron Lett. 2002, 43, 1-2.
  • 42
    • 3543136085 scopus 로고    scopus 로고
    • Statsuk, A. V.; Liu, D.; Kozmin, S. J. Am. Chem. Soc. 2004, 126, 95469547.
    • (g) Statsuk, A. V.; Liu, D.; Kozmin, S. J. Am. Chem. Soc. 2004, 126, 95469547.
  • 45
    • 33750320846 scopus 로고    scopus 로고
    • For a recent example of Au(I) alkyne spiroketalization: Liu, B.; De Brabander, J. K. Org. Lett. 2006, 8, 4907-4910.
    • For a recent example of Au(I) alkyne spiroketalization: Liu, B.; De Brabander, J. K. Org. Lett. 2006, 8, 4907-4910.
  • 46
    • 35548962903 scopus 로고    scopus 로고
    • For a strategically similar approach to the ABCD subunit, based on alkyne functionalization, see ref 6f
    • For a strategically similar approach to the ABCD subunit, based on alkyne functionalization, see ref 6f.
  • 51
    • 8344223214 scopus 로고    scopus 로고
    • 12 is obtained in two steps from commercially available 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose: Kozikowski, A. P.; Sorgi, K. L.; Wang, B. C.; Xu, Z. B. Tetrahedron Lett. 1983, 24, 1563-1566.
    • 12 is obtained in two steps from commercially available 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose: Kozikowski, A. P.; Sorgi, K. L.; Wang, B. C.; Xu, Z. B. Tetrahedron Lett. 1983, 24, 1563-1566.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.