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- 3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil. J. Gordon C. Hamilton, Antony M. Hooper, John A. Pickett, Kenji Mori, Satoshi Sano
, Chem. Commun.
, 1999
, 355
- Marine natural products. John W. Blunt, Brent R. Copp, Robert A. Keyzers, Murray H. G. Munro, Michèle R. Prinsep
, Nat. Prod. Rep.
, 2017
, 34
, 235
- Recent advances in chemical ecology. Jeffrey B. Harborne
, Nat. Prod. Rep.
, 1999
, 16
, 509
- Seven-membered ring annelation via Cope rearrangement of β-(2-vincyclopropyl)-αβ-unsaturated ketones: a new synthesis of (±)-β-himachalene. Edward Piers, Edward H. Ruediger
, J. Chem. Soc., Chem. Commun.
, 1979
, 166
- A new synthesis of a functionalized bicyclo[5.4.0]undecane skeleton based on a sequence involving [2 + 2] photoaddition and regioselective β-scission of alkoxyl radicals generated from the resulting cyclobutanols. Hiroshi Suginome, Yutaka Nakayama, Hiroyuki Harada, Hidefumi Hachiro, Kazuhiko Orito
, J. Chem. Soc., Chem. Commun.
, 1994
, 451
- 9-Methylgermacrene-B is confirmed as the sex pheromone of the sandfly Lutzomyia longipalpis from Lapinha, Brazil, and the absolute stereochemistry defined as S. J. Gordon C. Hamilton, Helen C. Ibbotson, Antony M. Hooper, John A. Pickett
, Chem. Commun.
, 1999
, 2335
- Biosynthesis of tutin. A. Corbella, P. Gariboldi, G. Jommi, C. Scolastico
, J. Chem. Soc. D
, 1969
, 634
- Natural sesquiterpenoids. B. M. Fraga
, Nat. Prod. Rep.
, 1994
, 11
, 533
- Cyclobutane based “overbred intermediates” and their exploration in organic synthesis. Monosij Nandy, Swagata Das, Samik Nanda
, Org. Biomol. Chem.
, 2022
, 20
, 1582
- Index pages
, Nat. Prod. Rep.
, 1984
, 1
, I1