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- 80. The constituents of natural phenolic resins. Part VIII. Lariciresinol, cubebin, and some stereochemical relationships. Robert D. Haworth, William Kelly
, J. Chem. Soc.
, 1937
, 384
- Synthetic transformation of hydroxymatairesinol from Norway spruce (Picea abies) to 7-hydroxysecoisolariciresinol, (+)-lariciresinol and (+)-cyclolariciresinol. Patrik Eklund, Reijo Sillanpää, Rainer Sjöholm
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 1906
- 227. The constituents of natural phenolic resins. Part XV. The stereochemical relationship of lariciresinol and pinoresinol. Robert D. Haworth, David Woodcock
, J. Chem. Soc.
, 1939
, 1054
- Radical cyclisation route to furanolignans: short and stereoselective synthesis of (±)-dihydrosesamin and (±)-lariciresinol. Gourhari Maiti, Sankar Adhikari, Subhas Chandra Roy
, J. Chem. Soc., Perkin Trans. 1
, 1995
, 927
- Scalemic natural products. Sarah Mazzotta, Vincenzo Rositano, Luca Senaldi, Anna Bernardi, Pietro Allegrini, Giovanni Appendino
, Nat. Prod. Rep.
, 2023
, 40
, 1647
- 346. The constitution of natural phenolic resins. Part IX. The structure of lariciresinol and preliminary experiments on the synthesis of lignandiols. Robert D. Haworth, William Kelly
, J. Chem. Soc.
, 1937
, 1645
- Umbelliprenin and lariciresinol isolated from a long-term-used herb medicine Ferula sinkiangensis induce apoptosis and G0/G1 arresting in gastric cancer cells. Lijing Zhang, Jianyong Si, Guangzhi Li, Xiaojin Li, Leilei Zhang, Li Gao, Xiaowei Huo, Dongyu Liu, Xiaobo Sun, Li Cao
, RSC Adv.
, 2015
, 5
, 91006
- Dissection of lignin macromolecular configuration and assembly: Comparison to related biochemical processes in allyl/propenyl phenol and lignan biosynthesis. Laurence B. Davin, Michaël Jourdes, Ann M. Patten, Kye-Won Kim, Daniel G. Vassão, Norman G. Lewis
, Nat. Prod. Rep.
, 2008
, 25
, 1015
- Lignans, neolignans and related compounds. Robert S. Ward
, Nat. Prod. Rep.
, 1997
, 14
, 43
- Metabolic analysis of the cinnamate/monolignol pathway in Carthamus tinctorius seeds by a stable-isotope-dilution method. Norikazu Sakakibara, Tomoyuki Nakatsubo, Shiro Suzuki, Daisuke Shibata, Mikio Shimada, Toshiaki Umezawa
, Org. Biomol. Chem.
, 2007
, 5
, 802