150 results on '"Huang, Jiann-Jyh"'
Search Results
2. Discovery of T-1101 tosylate as a first-in-class clinical candidate for Hec1/Nek2 inhibition in cancer therapy
3. Palladium‐catalyzed dual C–H activation of N‐phenyl‐1H‐indole‐3‐carboxamides for the synthesis of 5,11‐dihydro‐6H‐indolo[3,2‐c]quinolin‐6‐ones
4. Synthesis of Spirocyclopropane-Containing 4H-Pyrazolo[1,5-a]indoles via Alkylative Dearomatization and Intramolecular N-Imination of an Indole–O-(Methylsulfonyl)oxime
5. Supplementary Figures 1 through 6 from Activity of a Novel Hec1-Targeted Anticancer Compound against Breast Cancer Cell Lines In Vitro and In Vivo
6. Supplementary Materials and Methods, Supplementary Table 1, and Supplementary Figure Legends from Activity of a Novel Hec1-Targeted Anticancer Compound against Breast Cancer Cell Lines In Vitro and In Vivo
7. Synthesis of Spirocyclopropane-Containing 4 H -Pyrazolo[1,5- a ]indoles via Alkylative Dearomatization and Intramolecular N -Imination of an Indole– O -(Methylsulfonyl)oxime.
8. Recovery of spent alumina-supported platinum catalyst and reduction of platinum oxide via plasma sintering technique
9. Inhibition of Hec1 as a novel approach for treatment of primary liver cancer
10. Synthesis and structure–activity relationship of 3- O-acylated (–)-epigallocatechins as 5α-reductase inhibitors
11. An efficient and convenient transformation of α-haloketones to α-hydroxyketones using cesium formate
12. Improvement of the thermal latency for epoxy-phenolic resins by novel amphiphatic imidazole catalysts
13. Recovery and Reduction of Spent Alumina-Supported Cobalt–Molybdenum Oxide Catalyst via Plasma Sintering Technique
14. Design, synthesis, and in vitro/vivo anticancer activity of 4‐substituted 7‐(3‐fluoro‐4‐methoxybenzyl)‐7 H‐pyrrolo[2,3‐ d ]pyrimidines
15. Facile and efficient synthesis of 1-[2-(6,7-dimethyl-3,4-dihydronaphthalen-2-yl)ethyl]pyrrolidine hydrochloride
16. Recovery and Reduction of Spent Nickel Oxide Catalyst via Plasma Sintering Technique
17. Copper(I)-Catalyzed Nitrile-Addition/N-Arylation Ring-Closure Cascade: Synthesis of 5,11-Dihydro-6H-indolo[3,2-c]quinolin-6-ones as Potent Topoisomerase-I Inhibitors
18. The inhibition profiles of 4'‐acylpyrrole–5‐fluoroindolin‐2‐ones with a C‐3' side chain for VEGFR2, PDGFR‐β, and FGFR‐1 protein kinases
19. Os(CO) 2(η 2-SC 5H 4N(O))(η 2-SC 5H 4N): structural evidence for the transformation of pyridine-2-thione N-oxide to pyridine-2-thiolate in osmium complexes
20. The mechanism investigation in substitution of 21-bromo-3α-hydroxyl-3β-methoxymethyl-5α-pregnan-20-one with nucleophiles
21. Synthesis of 3α-hydroxy-21-(1′-imidazolyl)-3β-methoxyl-methyl-5α-pregnan-20-one via lithium imidazole with 17α-acetylbromopregnanone
22. Sodium bis(trimethylsilyl)amide and lithium diisopropylamide in deprotection of alkyl aryl ethers: alpha-effect of silicon
23. Design, synthesis, and in vitro/vivo anticancer activity of 4‐substituted 7‐(3‐fluoro‐4‐methoxybenzyl)‐7H‐pyrrolo[2,3‐d]pyrimidines.
24. ChemInform Abstract: Vilsmeier—Haack Reagent‐Promoted Formyloxylation of α‐Chloro‐N‐arylacetamides by Formamide.
25. Vilsmeier–Haack reagent-promoted formyloxylation of α-chloro-N-arylacetamides by formamide
26. Synthesis and antiproliferative evaluation of N,N-disubstituted-N′-[1-aryl-1H-pyrazol-5-yl]-methnimidamides
27. ChemInform Abstract: One-Flask Synthesis of 1,3,5-Trisubstituted 1,2,4-Triazoles from Nitriles and Hydrazonoyl Chlorides via 1,3-Dipolar Cycloaddition.
28. Discovery of 4-Aryl-N-arylcarbonyl-2-aminothiazoles as Hec1/Nek2 Inhibitors. Part I: Optimization of in Vitro Potencies and Pharmacokinetic Properties
29. Synthesis of 1,3,4-Oxadiazole-Based Aromatic and Heterocyclic/Phenylpyrazole Derivatives
30. Activity of a Novel Hec1-Targeted Anticancer Compound against Breast Cancer Cell Lines In Vitro and In Vivo
31. Characterization of the biological activity of a potent small molecule Hec1 inhibitor TAI-1
32. One-flask synthesis of 1,3,5-trisubstituted 1,2,4-triazoles from nitriles and hydrazonoyl chlorides via 1,3-dipolar cycloaddition
33. Design and synthesis of pyrrole–5-(2,6-dichlorobenzyl)sulfonylindolin-2-ones with C-3′ side chains as potent Met kinase inhibitors
34. Desulfurization and transformation of isothiocyanates to cyanamides by using sodium bis(trimethylsilyl)amide
35. Synthesis and Antiproliferative Activities of Ottelione A Analogues
36. Su2034 Inhibition of Hec-1 as a Novel Approach to the Treatment of Hepatocellular Carcinoma
37. Epigallocatechin-3-gallate prevents lupus nephritis development in mice via enhancing the Nrf2 antioxidant pathway and inhibiting NLRP3 inflammasome activation
38. ChemInform Abstract: Dibromination of 5‐Pyrazolones and 5‐Hydroxypyrazoles via Dibromoisocyanuric Acid.
39. Discovery of Pyrrole−Indoline-2-ones as Aurora Kinase Inhibitors with a Different Inhibition Profile
40. Dibromination of 5-pyrazolones and 5-hydroxypyrazoles via dibromoisocyanuric acid
41. ChemInform Abstract: “One‐Flask” Transformation of Isocyanates and Isothiocyanates to Guanidine Hydrochlorides by Using Sodium Bis(trimethylsilyl)amide.
42. One-pot ethynylation and catalytic desilylation in synthesis of mestranol and levonorgestrel
43. ChemInform Abstract: Synthesis of 2-Aryl-2H-[1,2,4]triazoloquinolin-3-one and 2-Aryl-2H-[1,2,4]triazoloisoquinolin-3-one Derivatives from α-Chloroformylarylhydrazines Hydrochloride.
44. ‘One-flask’ transformation of isocyanates and isothiocyanates to guanidines hydrochloride by using sodium bis(trimethylsilyl)amide
45. ChemInform Abstract: Efficient Dibromination of 5-Pyrazolones and 5-Hydroxypyrazoles by N-Bromobenzamide.
46. Synthesis of 2-aryl-2H-[1,2,4]triazoloquinolin-3-one and 2-aryl-2H-[1,2,4]triazoloisoquinolin-3-one derivatives from α-chloroformylarylhydrazines hydrochloride
47. ChemInform Abstract: An Efficient and Convenient Transformation of α‐Haloketones to α‐Hydroxyketones Using Cesium Formate.
48. Abstract A89: Synthesis and structure‐activity relationship of 3‐O‐acylated (−)‐epigallocatechins as 5α‐reductase inhibitors
49. Efficient di-bromination of 5-pyrazolones and 5-hydroxypyrazoles by N-bromobenzamide
50. ChemInform Abstract: Desulfurization and Transformation of Isothiocyanates to Cyanamides by Using Sodium Bis(trimethylsilyl)amide.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.