100041-67-6(100041-67-6)名称与标识符
100041-67-6(100041-67-6)相关文献
- 1. Cu-catalyzed mild and efficient oxidation of THβCs using air: application in practical total syntheses of perlolyrine and flazin
Bo Zheng,Tien Ha Trieu,Tian-Zhuo Meng,Xia Lu,Jing Dong,Qiang Zhang,Xiao-Xin Shi RSC Adv. 2018 8 6834 - 2. The alkaloids of perennial rye-grass (Lolium perenne L.). Part IV. Isolation of a new base, perlolyrine; the crystal structure of its hydrobromide dihydrate, and the synthesis of the base
J. A. D. Jeffreys J. Chem. Soc. C 1970 1091 - 3. Protective effects of Lycium barbarum L. berry extracts against oxidative stress-induced damage of the retina of aging mouse and ARPE-19 cells
Hui-li Zheng,Meng-ting Li,Tong Zhou,Ying-yi Wang,Er-Xin Shang,Yong-qing Hua,Jin-ao Duan,Yue Zhu Food Funct. 2023 14 399 - 4. Reusable, homogeneous water soluble photoredox catalyzed oxidative dehydrogenation of N-heterocycles in a biphasic system: application to the synthesis of biologically active natural products
S. Srinath,R. Abinaya,Arun Prasanth,M. Mariappan,R. Sridhar,B. Baskar Green Chem. 2020 22 2575 - 5. Visible light mediated selective oxidation of alcohols and oxidative dehydrogenation of N-heterocycles using scalable and reusable La-doped NiWO4 nanoparticles
R. Abinaya,K. Mani Rahulan,S. Srinath,Abdul Rahman,P. Divya,K. K. Balasubramaniam,R. Sridhar,B. Baskar Green Chem. 2021 23 5990 - 6. Natural carbolines inspired the discovery of chiral CarOx ligands for asymmetric synthesis and antifungal leads
Jixing Lai,Wei Li,Sanyue Wei,Shengkun Li Org. Chem. Front. 2020 7 2263 - 7. Simple indole alkaloids and those with a non-rearranged monoterpenoid unit
Minoru Ishikura,Takumi Abe,Tominari Choshi,Satoshi Hibino Nat. Prod. Rep. 2013 30 694 - 8. Antioxidant activity and inhibitory effects of 2-hydroxy-3-methylcyclopent-2-enone isolated from ribose–histidine Maillard reaction products on aldose reductase and tyrosinase
Seung Hwan Hwang,Zhiqiang Wang,Hong-Won Suh,Soon Sung Lim Food Funct. 2018 9 1790 - 9. A Review: Pharmacological Activity and Phytochemical Profile of Abelmoschus esculentus (2010–2022)
Marwa A. M. Abdel-Razek,Miada F. Abdelwahab,Usama Ramadan Abdelmohsen,Ashraf N. E. Hamed RSC Adv. 2023 13 15280 - 10. Index of subjects, 1970
J. Chem. Soc. C 1970 2733
![N'-[(Z)-(2-氧萘基-1-亚甲基)甲基]吡啶-4-碳酰肼](http://hg.y866.cn/compound/lib/scimg/cas/150/796-42-9.png "N'-[(Z)-(2-氧萘基-1-亚甲基)甲基]吡啶-4-碳酰肼")
![4-[2,4-双(三氟甲基)苄氧基]-3-甲氧基苯甲醛](http://hg.y866.cn/compound/lib/scimg/cas/150/796844-14-9.png "4-[2,4-双(三氟甲基)苄氧基]-3-甲氧基苯甲醛")
