151 results on '"Bando, Masahiko"'
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2. Tricalysiolide G and tricalysiols A and B: rearranged ent-kaurane-type and ent-kaurane-type diterpenoids from the leaves of Tricalysia dubia (Lindl.) Ohwi
3. Use of zinc enolate, free from other metals, in enantioselective palladium-catalyzed allylic alkylation
4. Tricalysiosides H–O: Ent-kaurane glucosides from the leaves of Tricalysia dubia
5. Lasianthionosides A–C, megastigmane glucosides from leaves of Lasianthus fordii
6. Enantioselective Synthesis of the Metabolites of Vasopressin V 2 Receptor Antagonist OPC-31260 via Lipase-Catalyzed Transesterification
7. Stereoselective synthesis of alkenylated malonic diamide using masked acyl cyanide
8. Novel sesquiterpene esters with alkaloid and monoterpene and related compounds from Tripterygium hypoglaucum: A new class of potent anti-HIV agents
9. Structure and synthesis of orobanchol, the germination stimulant for Orobanche minor
10. An efficient synthesis of pironetins employing a useful chiral building block,(1S,5S,6R)-5-hydroxybicyclo[4.1.0]heptan-2-one
11. Impact of the Dissolution Profile of the Cilostazol Cocrystal with Supersaturation on the Oral Bioavailability
12. Structural analysis of human glutamine:fructose-6-phosphate amidotransferase, a key regulator in type 2 diabetes
13. ChemInform Abstract: Stereoselective Synthesis of Alkenylated Malonic Diamide Using Masked Acyl Cyanide.
14. ChemInform Abstract: Structure and Synthesis of Orobanchol, the Germination Stimulant for Orobanche minor.
15. ChemInform Abstract: Plant Bioregulators. Part 3. Synthetic Disproof of the Structure Proposed for Alectrol, the Germination Stimulant from Vigna unguiculata.
16. ChemInform Abstract: An Efficient Synthesis of Pironetins Employing a Useful Chiral Building Block, (1S,5S,6R)-5-Hydroxybicyclo[4.1.0]heptan-2-one.
17. ChemInform Abstract: Plant Bioregulators. Part 4. Synthesis and Structure of Orobanchol, the Germination Stimulant for Orobanche Minor.
18. ChemInform Abstract: Pheromone Synthesis. Part 212. Synthesis of (1R,4R,5S)-(+)-Acoradiene, the Structure Proposed for the Aggregation Pheromone of the Broad-Horned Flour Beetle.
19. Crystal Structure Analysis of Human Glutamine: Fructose 6-Phosphate Amidotransferase, a Key Regulator in Type 2 Diabetes
20. Structural analysis of human glutamine:fructose‐6‐phosphate amidotransferase, a key regulator in type 2 diabetes
21. Tricalysiolide G and tricalysiols A and B: rearranged ent-kaurane-type and ent-kaurane-type diterpenoids from the leaves of Tricalysia dubia (Lindl.) Ohwi
22. Use of Zinc Enolate, Free from Other Metals, in Enantioselective Palladium-Catalyzed Allylic Alkylation.
23. Glochidiolide, Isoglochidiolide, Acuminaminoside, and Glochidacuminosides A—D from the Leaves of Glochidion acuminatum Muell.
24. Lasianthionosides A—C, Megastigmane Glucosides from Leaves of Lasianthus fordii
25. Synthesis and Stereochemistry of the Four Himachalene-Type Sesquiterpenes Isolated from the Flea Beetle (Aphthona flava) as Pheromone Candidates
26. Synthesis and determination of the absolute configuration of fudecalone
27. Glochidionionosides A-D: Megastigmane Glucosides from Leaves of Glochidion zeylanicum (Gaertn.) A. Juss.
28. Characterization of Orally Active Nonpeptide Vasopressin V2 Receptor Agonist. Synthesis and Biological Evaluation of Both the (5R)- and (5S)-Enantioisomers of 2-[1-(2-Chloro-4-pyrrolidin-1-yl-benzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin- 5-yl]-N-isopropylacetamide
29. Tricalysiosides A−G: Rearranged ent-Kauranoid Glycosides from the Leaves of Tricalysia dubia
30. Determination of the Stereochemistry of (−)-Koninginin A by an X-ray Analysis of Its Synthetic Sample
31. An Efficient Synthesis of a Key Inter- mediate for Vasopressin V2 Receptor Agonist OPC-51803 by Lipase-catalyzed Enantioselective Transesterification
32. Synthesis of (1R,4R,5S)-(+)-Acoradiene, the Structure Proposed for the Aggregation Pheromone of the Broad-Horned Flour Beetle
33. An Efficient Synthesis of Optical Isomers of Vasopressin V2 Receptor Antagonist OPC-41061 by Lipase-catalyzed Enantioselective Transesterification
34. The Studies of the Intramolecular C-F-H-N Hydrogen Bonding Using Covalently-Linked Base Pair Models of F and A
35. ChemInform Abstract: Enantioselective Synthesis of the Metabolites of Vasopressin V2 Receptor Antagonist OPC‐31260 via Lipase‐Catalyzed Transesterification.
36. ChemInform Abstract: Glochidionolactones A-F: Butenolide Glucosides from Leaves of Glochidion zeylanicum (GAERTN) A. JUSS.
37. ChemInform Abstract: A Conformationally Reliable Spacer for Molecular Tweezers.
38. Enantioselective Synthesis of the Metabolites of Vasopressin V2 Receptor Antagonist OPC-31260 via Lipase-Catalyzed Transesterification
39. ChemInform Abstract: Synthetic Microbial Chemistry. Part 32. Synthesis and Absolute Configuration of Hongoquercin A, an Antibacterial Sesquiterpene‐Substituted Orsellinic Acid Isolated as a Fungal Metabolite.
40. A Conformationally Reliable Spacer for Molecular Tweezers
41. Glochidionolactones A-F: Butenolide Glucosides from Leaves of Glochidion zeylanicum (GAERTN) A. JUSS.
42. Synthesis and Absolute Configuration of Hongoquercin A, an Antibacterial Sesquiterpene-Substituted Orsellinic Acid Isolated as a Fungal Metabolite
43. Pheromone Synthesis, CCVIII: Synthesis of (1S,3S,7R)-3-Methyl-α-himachalene, the Sex Pheromone of the Sandfly Lutzomyia longipalpis from Jacobina, Brazil
44. Conformational Difference between Mono- and Diprotonated cis-2,5-Diphenylpiperazinium Salts in the Solid State.
45. ChemInform Abstract: Plant Bioregulators. Part 2. Syntheses of (.+‐.)‐ and (+)‐Sorgolactone, the Germination Stimulant from Sorghum bicolor.
46. Synthesis and Structure of Orobanchol, the Germination Stimulant forOrobanche minor
47. Synthetic Disproof of the Structure Proposed for Alectrol, the Germination Stimulant fromVigna unguiculata
48. Syntheses of (±)- and (+)-Sorgolactone, the Germination Stimulant fromSorghum bicolor
49. Synthetic disproof against the structure proposed for alectrol, the germination stimulant from Vigna unguiculata
50. Synthesis of Stegobiol and Its Oxidation to Stegobinone, the Components of the Female-Produced Sex Pheromone of the Drugstore Beetle
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