Search Results - "Rivett, Douglas E.A"

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  1. 1

    The absolute stereochemistry of a diterpene from Ballota aucheri by Gray, Christopher A, Rivett, Douglas E.A, Davies-Coleman, Michael T

    Published in Phytochemistry (Oxford) (01-06-2003)
    “…The semi-synthetic transformation of hispanolone, isolated from Ballota africana, into 6β-hydroxy-15,16-epoxylabda-8,13(16),14-trien-7-one has established an…”
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  2. 2

    The Structure and Synthesis of Tsitsikammafuran: A New Furanosesquiterpene from a South African Dysidea Sponge by McPhail, Kerry L., Rivett, Douglas E.A., Lack, David E., Davies-Coleman, Michael T.

    Published in Tetrahedron (17-11-2000)
    “…Three furanosesquiterpenes, the new tsitsikammafuran ( 1) and the known nakafurans-8 ( 2) and -9 ( 3) were isolated from a South African Dysidea sponge. The…”
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  3. 3

    An improved synthesis of rhinocerotinoic acid by Gray, Christopher A, Davies-Coleman, Michael T, Rivett, Douglas E.A

    Published in Tetrahedron (06-01-2003)
    “…The stereoselective synthesis of E-rhinocerotinoic acid has been achieved in five steps from (−)-sclareol in an overall yield of 32%. This constitutes a…”
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  4. 4

    Transformations of hispanolone. Novel Michael adducts with in planta activity against rice blast by van Wyk, Albert W.W., Gray, Christopher A., Keyzers, Robert A., Rivett, Douglas E.A., Caira, Mino R., Nader, Bassam S., Davis, George E., Werk, Todd L., Davies-Coleman, Michael T.

    Published in Tetrahedron (29-08-2005)
    “…Two novel Michael adducts 9α-cyano-15,16-epoxy-7β-hydroxylabda-13(16),14-dien-6-one ( 2 ) and 9α-cyano-15,16-epoxy-7-hydroxylabda-7,13(16),14-trien-6-one ( 3 )…”
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  5. 5

    5,6-Dihydro-α-pyrones from Syncolostemon argenteus by Collett, Lynne A., Davies-Coleman, Michael T., Rivett, Douglas E.A.

    Published in Phytochemistry (Oxford) (01-06-1998)
    “…The chemical structures of five new α-pyrones, synargentolides A-E, isolated from Syncolostemon argenteus, have been established as 6 R-[4 R,5 R,6…”
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  6. 6

    5,6-Dihydro-α-pyrones from Syncolostemon parviflorus by Davies-Coleman, Michael T., Rivett, Douglas E.A.

    Published in Phytochemistry (Oxford) (1996)
    “…The chemical structure and absolute stereochemistry of three new α-pyrones, synparvolides A-C, isolated from Syncolostemon parviflorus, have been established…”
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  7. 7

    Absolute configuration of α-pyrones from Cryptocarya latifolia and Syncolostemon densiflorus by Collett, Lynne A., Davies-Coleman, Michael T., Rivett, Douglas E.A., Drewes, Siegfried E., Horn, Marion M.

    Published in Phytochemistry (Oxford) (01-03-1997)
    “…The stereochemical structures of two α-pyrones previously isolated from Cryptocarya latifolia have been shown to be 6 R-[2 R,4 S,6…”
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  8. 8

    Structure of the 5,6-dihydro-α-pyrone, umuravumbolide by Davies-Coleman, Michael T., Rivett, Douglas E.A.

    Published in Phytochemistry (Oxford) (01-02-1995)
    “…The structure and absolute stereochemisry of umuravumbolide and desacetylumuravumbolide have been elucidated by spectral means…”
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