Shigeki Seto
Publications by Year
Research Areas
Synthesis of heterocyclic compounds, Synthesis and Reactivity of Heterocycles, Phenothiazines and Benzothiazines Synthesis and Activities, Alkaloids: synthesis and pharmacology, Synthesis and Biological Evaluation
Most-Cited Works
- → Total Synthesis of Vinblastine, Vincristine, Related Natural Products, and Key Structural Analogues(2009)386 cited
- → Novel Seco Cyclopropa[c]pyrrolo[3,2-e]indole Bisalkylators Bearing a 3,3‘-Arylenebisacryloyl Group as a Linker(2001)40 cited
- → Design, synthesis, and evaluation of novel 2-substituted-4-aryl-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,5]oxazocin-5-ones as NK1 antagonists(2005)33 cited
- → Design and synthesis of novel 9-substituted-7-aryl-3,4,5,6-tetrahydro-2H-pyrido[4,3-b]- and [2,3-b]-1,5-oxazocin-6-ones as NK1 antagonists(2005)26 cited
- → Quinolone derivatives containing strained spirocycle as orally active glycogen synthase kinase 3β (GSK-3β) inhibitors for type 2 diabetics(2011)24 cited
- → 2-Substituted-4-aryl-6,7,8,9-tetrahydro-5H-pyrimido[4,5-b][1,5]oxazocin-5-one as a structurally new NK1 antagonist(2005)24 cited
- → Synthesis and structure–activity relationship of 4-quinolone-3-carboxylic acid based inhibitors of glycogen synthase kinase-3β(2011)23 cited
- → Novel pyrazolo[1,5-a]pyridines as orally active EP1 receptor antagonists: Synthesis, structure-activity relationship studies, and biological evaluation(2017)21 cited
- → The novel cyclopropapyrroloindole(CPI) bisalkylators bearing 3,3′-(1,4-phenylene)diacryloyl group as a linker(1998)19 cited
- → Discovery of novel pyrazolo[1,5-a]pyridine-based EP1 receptor antagonists by scaffold hopping: Design, synthesis, and structure-activity relationships(2017)18 cited