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- The chemistry of terpenes. Part 27. The halogenation of (+)-thujone and of (–)-carvotanacetone, and the stereochemistry and mechanism of formation of ‘tribromothujone’. Wesley Cocker, Patrick V. R. Shannon, Marion Dowsett
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 1527
- Opening of the cyclopropane ring of the thujan-3-ols in fluorosulphuric acid. John C. Rees, David Whittaker
, J. Chem. Soc., Perkin Trans. 2
, 1981
, 953
- Terpene biosynthesis. Part V. Interconversions of some monoterpenes in higher plants and their possible role as precursors of carotenoids. D. V. Banthorpe, Hilary J. Doonan, Ann Wirz-Justice
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 1764
- Stereochemistry of reduction of umbellulone (thuj-3-en-2-one) and isodihydroumbellulone (4βH-thujan-2-one). Collette M. Holden, John C. Rees, Stephen P. Scott, David Whittaker
, J. Chem. Soc., Perkin Trans. 2
, 1976
, 1342
- A three-step enantioselective synthesis of (+)- and (−)-α-thujone. Kellie L. Weeks, Jack D. Williams, Gregory R. Boyce
, Org. Biomol. Chem.
, 2021
, 19
, 8018
- A six-step total synthesis of α-thujone and d
6-α-thujone, enabling facile access to isotopically labelled metabolites. Irene Thamm, Johannes Richers, Michael Rychlik, Konrad Tiefenbacher
, Chem. Commun.
, 2016
, 52
, 11701
- 382. Researches in the thujone series. Part I. The thujones and some thujyl alcohols and thujylamines. Andrew G. Short, John Read
, J. Chem. Soc.
, 1938
, 2016
- Stereochemistry of reduction of (–)-thujone and (—)-isothujone. D. V. Banthorpe, H. ff. S. Davies
, J. Chem. Soc. B
, 1968
, 1356
- Vibrational optical activity for structural characterization of natural products. Prasad L. Polavarapu, Ernesto Santoro
, Nat. Prod. Rep.
, 2020
, 37
, 1661
- 223. Researches in the thujone series. Part II. The catalytic hydrogenation of d-sabinol. Andrew G. Short, John Read
, J. Chem. Soc.
, 1939
, 1040