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- Synthesis of spiroacetals using organoselenium-mediated cyclisation reactions. X-Ray molecular structure of (2S,8R)-8-methyl-2-phenyl-1,7-dioxaspiro[5.5]undecan-4(R)-ol. Annette M. Doherty, Steven V. Ley, Barry Lygo, David J. Williams
, J. Chem. Soc., Perkin Trans. 1
, 1984
, 1371
- Biosynthesis of insect spiroacetals. Yvonne K. Booth, William Kitching, James J. De Voss
, Nat. Prod. Rep.
, 2009
, 26
, 490
- Synthesis of the anti-Helicobacter pylori agent (+)-spirolaxine methyl ether and the unnatural (2″S)-diastereomer. James E. Robinson, Margaret A. Brimble
, Org. Biomol. Chem.
, 2007
, 5
, 2572
- Synthesis and absolute configuration of a constitutionally-new [5.6] spiroacetal from B. tryoni (Queensland fruit fly). Yvonne K. Booth, Patricia Y. Hayes, Christopher J. Moore, Lynette K. Lambert, William Kitching, James J. De Voss
, Org. Biomol. Chem.
, 2007
, 5
, 1111
- A diverse suite of spiroacetals, including a novel branched representative, is released by female Bactrocera tryoni (Queensland fruit fly). Yvonne K. Booth, Brett D. Schwartz, Mary T. Fletcher, Lynette K. Lambert, William Kitching, James J. De Voss
, Chem. Commun.
, 2006
, 3975
- Chemistry of fruit flies: composition of the male rectal gland secretions of some species of South-East Asian Dacinae. Re-examination of Dacus cucurbitae(melon fly). Michael V. Perkins, William Kitching, Richard A. I. Drew, Christopher J. Moore, Wilfried A. König
, J. Chem. Soc., Perkin Trans. 1
, 1990
, 1111
- Sex pheromone biosynthesis in the female olive fruit-fly. Double labelling from [18O2]-dioxygen into 1,7-dioxaspiro[5.5]undecane. Mary T. Fletcher, Basilis E. Mazomenos, John H. Georgakopoulos, Maria A. Konstantopoulou, Barry J. Wood, James J. De Voss, William Kitching
, Chem. Commun.
, 2002
, 1302