38 results on '"Arata Yajima"'
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2. Synthesis of both enantiomers of lycoperdic acid, an unusual mushroom-derived amino acid
3. Enantioselective synthesis and stereochemical determination of the highly reduced polyketide ishigamide
4. Practical synthesis of aromatic bisabolanes: Synthesis of 1,3,5-bisabolatrien-7-ol, peniciaculin A and B, and hydroxysydonic acid
5. Synthesis and stereochemistry of decarestrictines H and J
6. Synthesis and absolute configuration of formosusin A, a specific inhibitor of mammalian DNA polymerase β
7. Formal synthesis of cochlearol A, a meroterpenoid with renoprotective activity
8. Synthesis and stereochemistry of (−)-FE399
9. Synthesis of anti-Helicobacter pylori sesquiterpene employing tandem radical cyclization, and determination of the absolute configuration of the natural product
10. Stereoselective synthesis of (−)-decarestrictine G
11. How to Calculate the Number of Stereoisomers of Inositol Homologs
12. Total synthesis of epicoccamides A and D via olefin cross-metathesis
13. Concise Syntheses and Biological Activities of Ganomycin I and Fornicin A
14. Syntheses of 5′-O-desmethylterphenyllin and related p-terphenyls and their inhibitory activity of TNF-α release from RBL-2H3 cells
15. Total synthesis of virgineone aglycone and stereochemical assignment of natural virgineone
16. ChemInform Abstract: Synthesis and Absolute Configuration of Formosusin A, a Specific Inhibitor of Mammalian DNA Polymerase β
17. Synthesis of two osteoclast-forming suppressors, demethylincisterol A3 and chaxine A
18. Synthetic Study of Versipelostatin A: Synthesis of the Spirotetronate Unit Starting from Pulegone
19. Syntheses of the four stereoisomers of Phytophthora mating hormone α2 and a concise synthesis of mating hormone α1
20. Synthesis of (2RS,8R,10R)-YM-193221 and an Improved Approach to Tyroscherin, Bioactive Natural Compounds from Pseudallescheria sp
21. Asymmetric Total Synthesis ofent-Sandaracopimaradiene, a Biosynthetic Intermediate of Oryzalexins
22. Asymmetric synthesis of abietane diterpenoids via B-alkyl Suzuki–Miyaura coupling. Formal total asymmetric synthesis of 12-deoxyroyleanone and cryptoquinone
23. Direct determination of the stereoisomer constitution by 2D-HPLC and stereochemistry–pheromone activity relationship of the copulation release pheromone of the cowpea weevil, Callosobruchus maculatus
24. Synthesis of Sphingosine Relatives, XVIII!. Synthesis of Penazetidine A, an Alkaloid Inhibitor of Protein Kinase C Isolated from the Marine Sponge Penares sollasi
25. Synthesis of Mono- and Sesquiterpenoids, XXV. Synthesis of (6R*,7R*)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the Racemate of the Antibacterial Sesquiterpene from Premna oligotricha, and Its (6R*,7S*) Isomer
26. ChemInform Abstract: Total Synthesis of Epicoccamides A (Ia) and D (Ib) via Olefin Cross-Metathesis
27. A new sesquiterpenoid produced by female Callosobruchus rhodesianus (Pic): a possible component of the sex attractant pheromone
28. Absolute configuration of phytocassanes as proposed on the basis of the CD spectrum of synthetic (+)-2-deoxyphytocassane A
29. Synthetic Microbiol Chemistry, XXIX!. Synthesis of Both the Enantiomers of Incrustoporin, an Antibiotic from Incrustoporia carneola
30. Total synthesis of ent-cassa-12,15-diene, a putative precursor of rice phytoalexins, phytocassanes A–E
31. Synthesis and stereochemistry-activity relationship of small bacteriocin, an autoinducer of the symbiotic nitrogen-fixing bacterium Rhizobium leguminosarum
32. Efficient and stereo-selective syntheses of three stereoisomers of the sex pheromone of the cowpea weevil, Callosobruchus maculatus
33. Asymmetric Synthesis of Abietane Diterpenoids via B-Alkyl Suzuki—Miyaura Coupling. Formal Total Asymmetric Synthesis of 12-Deoxyroyleanone (Ia) and Cryptoquinone (Ib)
34. Synthesis of Cordiaquinone J and K via B-Alkyl Suzuki—Miyaura Coupling as a Key Step and Determination of the Absolute Configuration of Natural Products
35. Synthesis and Absolute Configuration of Cordiaquinone K, Antifungal and Larvicidal Meroterpenoid Isolated from the Panamanian Plant, Cordia curassavica
36. Synthesis and absolute configuration of MQ-A3 [1-(14'-methylhexadecanoyl) pyrrolidine], a novel aliphatic pyrrolidine amide from the tropical convolvulaceous species
37. Determination of the Absolute Configuration of the Biologically Active Natural Product by Ohrui-Akasaka Method
38. Corrigendum to 'Synthesis and absolute configuration of cordiaquinone K, antifungal and larvicidal meroterpenoid isolated from the Panamanian plant, Cordia curassavica'
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