144 results on '"Ueda, Yasutsugu"'
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2. Synthesis of novel nocathiacin-class antibiotics. Condensation of glycolaldehyde with primary amides and tandem reductive amination of Amadori-rearranged 2-oxoethyl intermediates
3. Mild method for cleavage of dehydroalanine units: highly efficient conversion of nocathiacin I to nocathiacin IV
4. The discovery and preclinical evaluation of BMS-707035, a potent HIV-1 integrase strand transfer inhibitor
5. Synthesis and evaluation of C2-carbon-linked heterocyclic-5-hydroxy-6-oxo-dihydropyrimidine-4-carboxamides as HIV-1 integrase inhibitors
6. Michael addition of amines and thiols to dehydroalanine amides: a remarkable rate acceleration in water
7. In Vitro Antiviral Characteristics of HIV-1 Attachment Inhibitor BMS-626529, the Active Component of the Prodrug BMS-663068
8. Inhibitors of Human Immunodeficiency Virus Type 1 (HIV-1) Attachment 6. Preclinical and Human Pharmacokinetic Profiling of BMS-663749, a Phosphonooxymethyl Prodrug of the HIV-1 Attachment Inhibitor 2-(4-Benzoyl-1-piperazinyl)-1-(4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-oxoethanone (BMS-488043)
9. ChemInform Abstract: Novel C‐Acylated Triazole Derivatives of Ravuconazole, an Azole Antifungal Agent.
10. Novel C‐acylated triazole derivatives of ravuconazole, an azole antifungal agent
11. Synthesis and antibacterial activity of nocathiacin I analogues
12. Envelope Conformational Changes Induced by Human Immunodeficiency Virus Type 1 Attachment Inhibitors Prevent CD4 Binding and Downstream Entry Events
13. Synthesis, in vitro, and in vivo antibacterial activity of nocathiacin I thiol-Michael adducts
14. Chemical Conversion of Nocathiacin I to Nocathiacin II and a Lactone Analogue of Glycothiohexide α
15. Nocathiacin I analogues: synthesis, in vitro and in vivo biological activity of novel semi-synthetic thiazolyl peptide antibiotics
16. Antimicrobial Evaluation of Nocathiacins, a Thiazole Peptide Class of Antibiotics
17. Synthesis and antibacterial activity of O-substituted nocathiacin I derivatives
18. Michael Addition of Amines and Thiols to Dehydroalanine Amides: A Remarkable Rate Acceleration in Water.
19. Corrigendum to “Organic reactions in frozen water: Michael addition of amines and thiols to the dehydroalanine side chain of nocathiacins”
20. Organic reactions in frozen water: Michael addition of amines and thiols to the dehydroalanine side chain of nocathiacins
21. Novel semi-synthetic nocathiacin antibiotics: synthesis and antibacterial activity of bis- and mono-O-alkylated derivatives
22. Phosphonooxymethyl prodrugs of the broad spectrum antifungal azole, ravuconazole: Synthesis and biological properties
23. Mild Method for Cleavage of Dehydroalanine Units: Highly Efficient Conversion of Nocathiacin I (Ia) to Nocathiacin IV (Ib).
24. A STUDY ON ARCHITECT KAZUE YAKUSHIJI AND ART DECO STYLE : A study on architectural design of the Kouji Fujioka's residence and the Magosaburou Oohara's residence, the Yuurinsou
25. Study of Road Snow Melting Using Exhausted Heat of Vehicle - Laboratory Experiments and Their Application Prospects
26. A Practical Synthesis of an Anti-Methicillin Resistant Staphylococcus aureus Cephalosporin BMS-247243
27. A STUDY ON ARCHITECT KAZUE YAKUSHIJI AND ART DECO STYLE : A study about interior design of the former head office of Chugoku Bank
28. ARCHITECT KAZUE YAKUSHIJI'S HISTORY AND HIS WORKS
29. Synthesis and structure-activity relationship of C-3 quaternary ammonium cephalosporins exhibiting anti-MRSA activities
30. Synthesis and structure-activity relationship of C-3 benzoyloxymethyl cephalosporins exhibiting anti-MRSA activities
31. Novel, water-soluble phosphate derivatives of 2′-ethoxy carbonylpaclitaxel as potential prodrugs of paclitaxel: Synthesis and antitumor evaluation
32. Synthesis and antitumor evaluation of 2′-oxycarbonylpaclitaxels (paclitaxel-2′-carbonates)
33. Synthesis and in vitro antibacterial activity of new semi-synthetic noviosylcoumarin antibiotics: chemical modification at the C-3′ ester
34. Novel water soluble phosphate prodrugs of taxol® possessing in vivo antitumor activity
35. Synthesis and in vitro activity of novel quaternary ammonium carbapenems: 2-Pyridiniopropyl and 1-pyridinioethyl carbapenems.
36. Inhibitors of Human ImmunodeficiencyVirus Type 1(HIV-1) Attachment 6. Preclinical and Human Pharmacokinetic Profilingof BMS-663749, a Phosphonooxymethyl Prodrug of the HIV-1 AttachmentInhibitor 2-(4-Benzoyl-1-piperazinyl)-1-(4,7-dimethoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-oxoethanone (BMS-488043)
37. Michael Addition of Amines and Thiols to Dehydroalanine Amides: A Remarkable Rate Acceleration in Water.
38. Mild Method for Cleavage of Dehydroalanine Units: Highly Efficient Conversion of Nocathiacin 1 to Nocathiacin IV.
39. In VitroAntiviral Characteristics of HIV-1 Attachment Inhibitor BMS-626529, the Active Component of the Prodrug BMS-663068
40. Nuclear analogs of β-lactam antibiotics. XV. Synthesis of 6-substituted 2-methylpenem-3-carboxylic acids.
41. Water Soluble Steroids with Catalytic Substituents II. Synthesis of 3β-(4(5)-Imidazolyl)-5α-androstane-11β, 17β,-diamine and Comparison of its Catalytic Properties with Those of 17β-(4(5)-Imidazolyl)-5α-androstane-3β, 11β-diamine
42. Synthesis and in vitro activity of several new carbapenems.
43. A simple method of preparing trimethylsilyl- and tert-butyldimethylsilyl-enol ethers of α-diazoacetoacetates and their use in the synthesis of a chiral precursor to thienamycin analogs.
44. Nuclear analogs of β-lactam antibiotics. XIX. Syntheses of racemic and enantiomeric p-nitrobenzyl carbapen-2-em-3-carboxylates.
45. Nuclear analogs of (β-lactam antibiotics. XVIII. A short synthesis of 2-alkylthiocarbapen-2-em-3-carboxylate.
46. A catalyst for ester hydrolysis showing electrostatic and hydrophobic binding properties
47. An efficient enantioselective synthesis of the carbapenam-2-one system. An approach to (+)-thienamycin and related carbapenems
48. SKELETAL REARRANGEMENT IN DEHYDROGENATION OF THUJOPSENE AND ITS CONGENERS
49. New Enzyme Model Systems
50. Nuclear analogs of β-lactam antibiotics. XIV. Synthesis of penems via (4-tritylthio-2-azetidinon-1-yl)triphenylphosphoranylideneacetates.
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