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- CCCXXXI.—The constituents of some Indian essential oils. Part XXV. 1-α- and 1-β-Curcumenes. B. Sanjiva Rao, John Lionel Simonsen
, J. Chem. Soc.
, 1928
, 2496
- 180. The structure of γ-curcumene. R. D. Batt, S. N. Slater
, J. Chem. Soc.
, 1949
, 838
- Volatile components in Yinchenzhufu decoction and their pharmacokinetics after oral administration in rats. Bin Zan, Yuanyuan Li, Xiaoshu Sun, Tianming Wang, Rong Shi, Yueming Ma
, RSC Adv.
, 2022
, 12
, 3287
- 317. The constituents of some Indian essential oil. Part XXVI. The structures of 1-α- and β-curcumenes. F. D. Carter, F. C. Copp, B. Sanjiva Rao, J. L. Simonsen, K. S. Subramaniam
, J. Chem. Soc.
, 1939
, 1504
- 532. Reduction by dissolving metals. Part VI. Some applications in synthesis. A. J. Birch, S. M. Mukherji
, J. Chem. Soc.
, 1949
, 2531
- Tandem Peterson olefination and chemoselective asymmetric hydrogenation of β-hydroxy silanes. Suppachai Krajangsri, Haibo Wu, Jianguo Liu, Wangchuk Rabten, Thishana Singh, Pher G. Andersson
, Chem. Sci.
, 2019
, 10
, 3649
- Application of the lithiation–borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes. Varinder K. Aggarwal, Liam T. Ball, Simon Carobene, Rickki L. Connelly, Matthew J. Hesse, Benjamin M. Partridge, Philippe Roth, Stephen P. Thomas, Matthew P. Webster
, Chem. Commun.
, 2012
, 48
, 9230
- Terpene synthases in disguise: enzymology, structure, and opportunities of non-canonical terpene synthases. Jeffrey D. Rudolf, Chin-Yuan Chang
, Nat. Prod. Rep.
, 2020
, 37
, 425
- Carboxy-directed asymmetric hydrogenation of α-alkyl-α-aryl terminal olefins: highly enantioselective and chemoselective access to a chiral benzylmethyl center. Shuang Yang, Shou-Fei Zhu, Na Guo, Song Song, Qi-Lin Zhou
, Org. Biomol. Chem.
, 2014
, 12
, 2049
- Bacterial terpenome. Jeffrey D. Rudolf, Tyler A. Alsup, Baofu Xu, Zining Li
, Nat. Prod. Rep.
, 2021
, 38
, 905