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Faculty Of Pharmaceutical Sciences | 論文
- Improved Procedure for N-Formylation of Amines to Formamides Using Formic Acid, Oxalyl Chloride and Imidazole
- Convenient One-Pot Method for Formylation of Amines and Alcohols Using Formic Acid and 1,1'-Oxalyldiimidazole
- Degradation of 3-Aryl-2-hydroxyiminopropionic Acids into Arylacetonitriles Using 1,1'-Carbonyldiimidazole or 2,2'-Oxalyldi(o-sulfobenzimide)
- An Improved Method for the Synthesis of Arylacetonitriles from 3-Aryl-2-hydroxyiminopropionic Acids Using 1,1'-Oxalyldiimidazole
- A Convenient One-Pot Preparation of Nitriles from Aldoximes Using 2,2'-Oxalyldi(o-sulfobenzimide)
- Convenient Synthesis of Amides, Esters, and Thioesters Using 2,2'-Oxalyldi(2,3-dihydro-3-oxobenzisosulfonazole)
- Synthesis of Furan Derivatives. LXXXIV. Kinetic Studies of the Curtius Rearrangement of 5-Substituted 2-Furoyl Azides and Related Compounds
- Synthesis of Furan Derivatives. LXXXIII. Kinetics of Acyl Azide Formation of Carboxylic Acids with Diphenyl Phosphorazidate
- Synthesis of Furan Derivatives. Synthesis of Furanpolycarboxylic Acid
- Synthesis of Furan Derivatives. LVII. The Reaction of Keto Acetylenic Esters with Carbonyl Reagents
- Synthesis of Fluorine Analogs of Protoporphyrin Potentially Useful for Diagnosis and Therapy of Cancer. IV.Synthesis of (Trifluorovinyl)vinyl-and (1-Chloro-2,2-difluorovinyl)vinyldeuteroporphyrins
- A New Pentanorlanostane Derivative, Cladosporide A, as a Characteristic Antifungal Agent against Aspergillus fumigatus, Isolated form Cladosporium sp.
- Effect of Arylthiolated 2,3-Dimethoxy-1,4-benzoquinones on Respiratory Activity and Lipid Peroxidation in Bovine Heart Mitochondria
- The Structure-Activity Relationship of [Dmt^1]Endomorphin-2 Derivatives
- The Influence of a Parotid Hypocalcemic Substance on the Levels of Calcium, Inorganic Phosphate, and Hydroxyproline in Rabbit Serum
- Circular Dichroism of a Hypocalcemic Protein in Bovine Parotid Gland
- Effect of Parotid Gland Hypocalcemic Factor on Increasing Antibody-producing Cells in Mice
- Synthesis in the Diazasteroid Group. XVII. Syntheses of the 4,11-Diazasteroid System
- Reaction of Vinylogous Esters with Grignard Reagent
- Synthesis in the Diazasteroid Group. IV. A Synthesis of 2,3-Dimethoxy-8,14-diaza-15-oxo-gona-1,3,5 (10)-triene
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