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Volumn 46, Issue 3, 2014, Pages 214-251

The phomactin natural products from isolation to total synthesis: A review

Author keywords

[No Author keywords available]

Indexed keywords

NATURAL PRODUCTS; TOTAL SYNTHESIS;

EID: 84901595819     PISSN: 00304948     EISSN: 19455453     Source Type: Journal    
DOI: 10.1080/00304948.2014.903142     Document Type: Review
Times cited : (15)

References (75)
  • 25
    • 85197969837 scopus 로고    scopus 로고
    • and references cited therein
    • Y. Ishihara, P. S. Baran, Synlett, 1733 (2010), and references cited therein.
    • (2010) Synlett , vol.1733
    • Ishihara, Y.1    Baran, P.S.2
  • 26
    • 85197978427 scopus 로고    scopus 로고
    • Please note that for the sake of simplicity, phomactin A carbon numbering is used throughoutthe discussion B, C and D are different from the phomactin A carbon numbering scheme (seereference 2
    • Please note that for the sake of simplicity, phomactin A carbon numbering is used throughoutthe discussion. However, even though the carbon skeleton is the same, the carbon assignmentsin phomactins B, C and D are different from the phomactin A carbon numbering scheme (seereference 2).
    • However, even though the Carbon Skeleton Is the Same, the Carbon Assignmentsin Phomactins
  • 38
    • 64649100805 scopus 로고    scopus 로고
    • For the development of the [ 23]-Wittig rearrangement and its application to a precursor of thephomactins
    • For the development of the [2,3]-Wittig rearrangement and its application to a precursor of thephomactins, see: P. D. P. Shapland and E. J. Thomas, Tetrahedron, 65, 4201 (2009).
    • (2009) Tetrahedron , vol.65 , pp. 4201
    • Shapland, P.D.P.1    Thomas, E.J.2
  • 40
    • 85197980730 scopus 로고    scopus 로고
    • Using different intermediates, the group was able to install the epoxide group chemo-anddiastereoselectively (see ref. 38
    • Using different intermediates, the group was able to install the epoxide group chemo-anddiastereoselectively (see ref. 38).
  • 46
    • 0346727417 scopus 로고    scopus 로고
    • For a review of the synthetic efforts towards phomactin A
    • For a review of the synthetic efforts towards phomactin A, see: K. P. Cole and R. P. Hsung,ChemTracts, 16, 811 (2003).
    • (2003) Chem Tracts , vol.16 , pp. 811
    • Cole, K.P.1    Hsung, R.P.2
  • 55
    • 80052140885 scopus 로고    scopus 로고
    • For overviews of Hsung's total synthesis of phomactin A, se and reference 56
    • For overviews of Hsung's total synthesis of phomactin A, see: G. S. Buchanan, K. P. Cole, Y.Tang and R. P. Hsung, J. Org. Chem., 76, 7027 (2011), and reference 56.
    • (2011) J. Org. Chem. , vol.76 , pp. 7027
    • Buchanan, G.S.1    Cole, K.P.2    Tang, Y.3    Hsung, R.P.4
  • 58
    • 29744436121 scopus 로고    scopus 로고
    • For additional studies toward the total synthesis of phomactin Asee
    • For additional studies toward the total synthesis of phomactin A, see: K. P. Cole and R. P. Hsung,Chem. Comm., 5784 (2005).
    • (2005) Chem. Comm. , pp. 5784
    • Cole, K.P.1    Hsung, R.P.2
  • 63
    • 0037486826 scopus 로고    scopus 로고
    • For reviews, see references 59 and 60
    • For reviews, see: A. Furstner, Chem. Rev., 99, 991 (1999); references 59 and 60.
    • (1999) Chem. Rev. , vol.99 , pp. 991
    • Furstner, A.1
  • 68
    • 33845376296 scopus 로고
    • For a review, see
    • For a review, see: T. Nakai and K. Mikami, Chem. Rev., 86, 885 (1986).
    • (1986) Chem. Rev. , vol.86 , pp. 885
    • Nakai, T.1    Mikami, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.