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Department of Applied Chemistry, Faculty of Engineering Saitama University | 論文
- Topochemical Photopolymerization of 4-[2-(Unsubstituted and Methyl-Substituted Pyrazinyl)ethenyl]cinnamates and -thiocinnamates in the Crystalline State
- Chemical Modification of Amide-Based Catenanes and Rotaxanes II. Synthesis of tertiary Amine [2]Catenanes and [2] Rotaxanes via N-Methylation Followed by Borane Reduction of Secondary Amide [2] Catenanes and [2] Rotaxanes and Mobility of Their Components
- Synthesis and Structure of [2]Catenated tertiary Octamide and Octamine
- Highly Regioselective Pinacol Rearrangement of Sulfenylmethylated Glycols
- The Cationic Diels-Alder Reaction, Facile Formation of Cationic Species from 2-Oxoalkyl Esters
- Regio-and Stereoselective Synthesis of a trans-4-[60]Fullerenobisacetic Acid Derivative by a Tether-Directed Biscyclopropanation: A Diacid Component Applicable for the Synthesis of Regio- and Stereo-Regular [60]Fullerene Pearl-Necklace Polyamides
- Formation of Ketones from Alkyl Nitrites in the Solid State
- Stereoselective Addition Reaction of Organolithium Reagents to Chiral Imines Derived from erythro-2-Amino-1,2-diphenylethanol
- Diastereoselective Synthesis of β-Amino Esters by the Lewis Acid-Mediated Reaction of N-Tosyl Aldimines with Ketane Bis(trimethylsilyl) Acetals
- Novel Copolyamides Containing [60]Fullerene in the Main Chain
- Unusual Demethylation of O,O'-Dimethyl Chlorothiophosphate with Aryllithiums
- Synthesis of Chiral Oligopeptides Which Recognize Double-Stranded DNAs
- Solid-phase Synthesis of a Novel Polyester Analog of Nucleic Acids Bearing a Serine Backbone Using a Linker which Cleaved under Neutral Conditions
- Synthesis of Chiral Oligopeptides Which Recognize Double-Stranded DNAs
- Solid-Phase Synthesis of a Novel Polyester Analog of Nucleic Acid Bearing Serine Backbone
- cis-2-Amino-3, 3-dimethyl-1-indanol : Application as a Highly Efficient Chiral Auxiliary for the Diels-Alder Reaction
- α-Sulfenyl-Directed Ring-Opening Reactions of Epoxides. 1. Highly Regio- and Stereoselective Reaction with Organo-Aluminum Reagents and Application to the Synthesis of an Aggregation Pheromone
- Synthesis of Novel Chiral Diamino Acid-based Polyamide as Analogues of Nucleic Acids
- Optical resolution of 2-amino-1,2-diphenylethanol by preferential crystallization and its utilization in fractional crystallization and enantioselective reduction of prochiral ketones.
- Improved optical resolution of (.+-.)-1,2-diphenylethylenediamine.