Purines. V. The Dimroth Rearrangement of 1-Alkoxyadenines : The Synthesis of N-Alkoxyadenines
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概要
- 論文の詳細を見る
- 公益社団法人日本薬学会の論文
- 1971-08-25
著者
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佐藤 忠夫
Faculty Of Pharmaceutical Sciences Chiba University
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板谷 泰助
Faculty of Pharmaceutical Sciences, Kanazawa University
関連論文
- Decarboxylative C-S Bond Formation. Synthesis of 1,4-Dimethyl-3,6-epidithio-2,5-piperazinedione and Related Compounds
- Synthesis of 3,6-Diethoxycarbonyl-3,6-epidithia-1,4-dimethyl-2,5-piperazinedione and Related Compounds. Formation of C-S Bond by the Reaction of Carbanion and Sulfur Monochloride
- Purines. LXX. An Extension of the "Phenacylamine Route" to the Syntheses of the 7-N-Oxides of 6-Mercaptopurine and 6-Methylthiopurine, and Antileukemic Activity of Some Purine N-Oxides
- Purines. LXIX. Direct N(1)-Oxidation of 7-Benzyladenine and Stepwise Syntheses of Its N(1)- and N(3)-Oxides
- Purines. LXVIII. Trifluoroperoxyacetic Acid Oxidation of N^6-Benzyladenine : Formation of the N(3)-Oxide and N(7)-Oxide, and Their Cytokinin Activities
- Purines. LXVII. An Alternative Synthesis of Adenine 7-Oxide : N-Oxidation of the Adenine Ring Utilizing Blocking/Deblocking at the 1-Position
- Purines. LXVI. Adenine 7-Oxide : Its Synthesis, Chemical Properties, and X-ray Molecular Structure
- Purines. LII. Synthesis and Biological Evaluation of 8-Methylguanine 7-Oxide and Its 9-Arylmethyl Derivatives
- Purines. LI. Synthesis and Biological Activity of Hypoxanthine 7-N-Oxide and Related Compounds
- Purines. L. Synthesis and Antileukemic Activity of the Antibiotic Guanine 7-Oxide and Its 9-Substituted Derivatives
- Stereochemical Studies. XXIII. Stereochemistry of the Thermal Isocyanide-Cyanide Rearrangement
- FORMATION OF CYCLIC CARBONATES IN THE REACTIONS OF 1,2-GLYCOLS WITH OXALYL CHLORIDE
- Purines. XXI. Synthesis of Adenine 1-Oxides Carrying an Allylic Side Chain at the 9-Position
- Stereochemical Studies. XXII. Thermal Rearrangement of S(-)-1-Phenylethyl Isocyanide
- Synthesis of 3-β-D-Ribofuranosylwye, the Most Probable Structure for Wyosine from Torulopsis utilis Phenylalanine Transfer Ribonucleic Acid
- Synthesis of 5-(Methylamino)-1-β-D-ribofuranosylimidazole-4-carboxamide, a Synthetic Intermediate for 3-Methyl-9-β-D-ribofuranosylpurines
- An Improved Procedure for the Synthesis of 1-Alkyl-5-(alkylamino)-imidazole-4-carboxamides, Synthetic Intermediates for 3,9-Dialkylpurine Derivatives
- Synthesis of N, N, 3,9-Tetraalkyladeninium Halides by Alkylations of N, N, 3- and N, N, 9-Trialkyladenines
- Purines. XXXV. : Synthesis and Cytokinin Activity of Racemic 1'-Methylzeatin
- Purines. XXXIII. Syntheses and Cytokinin Activities of Both Enantiomers of 1'-Methylzeatin and Their 9-β-D-Ribofuranosides
- Studies towards the Synthesis of the Fluorescent Bases of Phenylalanine Transfer Ribonucleic Acids : Synthesis of 7-(2-Hydroxy-3-methylbutyl)wye, a Model for the Minor Base Isolated from Rat Liver
- Purines. XIX. The Direct N^6-Alkylation of 1-Alkoxy-9-alkyladenines : An Alternative Synthesis of N^6,9-Dialkyladenines
- Wittig Reaction with N-Protected 3-(Triphenylphosphonio)alaninates : Synthesis of Optically Active (E)-(2-Arylvinyl)glycine Derivatives
- Synthesis and Absolute Configuration of Wybutine, the Fluorescent Minor Base from Phenylalanine Transfer Ribonucleic Acids
- Purines. XLVI. Preparation of 1-Ethyladenine from Adenosine
- 3,9-Dialkylhypoxanthines
- Purines. V. The Dimroth Rearrangement of 1-Alkoxyadenines : The Synthesis of N-Alkoxyadenines
- Synthesis of 5-(Alkylamino)-1-β-D-ribofuranosyl-1H-imidazole-4-carboxamides : Key Intermediates for the Synthesis of 3-Alkyl-9-β-D-ribofuranosylpurine Derivatives
- Purines. XXXII. : Synthesis and Ring Fission of 3,9-Dialkyladenines
- Purines. XXIX. Syntheses of 9-Alkyl-2-deuterio-N^6-methoxyadenines and 2-Deuterio-N^6,9-dimethyladenine : Tautomerism in 9-Substituted N^6-Alkoxyadenines(Organic,Chemical)
- Purines. XXV. Fission and Reclosure of the Adenine Ring by the Use of Modified Benzyloxy Groups at the 1-Position
- Purines. XXII. Methylation of 1-, 3-, 7-, 9-, and N^6-Methyladenines Bearing a Methoxyl Group at the N^6-Position : A Synthesis of 7,9-Dimethyladenine
- Purines. XX. Synthesis of 1-Substituted 5-Aminoimidazole-4-carboxamidines and Related Compounds
- Syntheses of N, N, 3- and N, N, 9-Trialkyladenines by Alkylation of N, N-Dialkyladenines
- Studies towards the Synthesis of the Fluorescent Bases of Phenylalanine Transfer Ribonucleic Acids : Synthesis of 7-Methylwye Isolated from Extremely Thermophilic Archaebacteria
- Ind. -N-Alkylation of Tryptophan and Synthesis of 1-Alkyltryptophan Hydrazides
- The Heck Reaction of N-Protected Vinylglycines with 4-Iodoanisole
- Syntheses of Optically Active, Protected and Unprotected Vinylglycines
- 3-Methylisoguanosine : Synthesis and Acidic Hydrolysis of the Glycosyl Bond
- Synthesis of 7-Methyl-3-β-D-ribofuranosylwye, the Putative Structure for the Hypermodified Nucleoside Isolated from Archaebacterial Transfer Ribonucleic Acids
- An Improved Procedure for the Synthesis of 1-Alkyladenines : Removal of the Ribofuranosyl Group from 1-Benzyl-, 1-(3-Methyl-2-butenyl)-, and 1-Allyladenosine Hydrobromide in Acetic Acid
- Purines. XV. Conversion of N, 9-Dimethyladenine into the 1,9-Dimethyl Isomer : A Reverse Operation of the Dimroth Rearrangement
- Improved Synthesis of 3-Methylguanine
- Purines. X. A Convenient Method for Synthesis of 2', 3'-O-Isopropylidene-adenosine 1-Oxide
- Purines. XVIII. Kinetic Studies of the Dimroth Rearrangement of 1-Alkoxy-9-methyladenines and 1-Benzyloxyadenosine : Effect of 1-Benzyloxy and 9-β-D-Ribofuranosyl Groups on the Rates of the Ring-opening and the Reclosure
- Purines. XVI. One-Step Alkylation of Adenine 1-Oxide Leading to 1-Alkoxy-9-alkyladenine Hydriodide
- 3-Methylxanthosine : Synthesis and Acidic Hydrolysis of the Glycosyl Bond
- SYNTHESIS OF 7-METHYL-3-β-D-RIBOFURANOSYLWYE, THE MOST PROBABLE STRUCTURE FOR THE FLUORESCENT NUCLEOSIDE ISOLATED FROM ARCHAEBACTERIAL TRANSFER RIBONUCLEIC ACIDS(Communications to the Editor)
- 3-Methylinosine
- Purines. XII. Catalytic Hydrogenolysis of Alkoxyaminopurines and Related Derivatives
- Purines. XI. The Synthesis of N-Alkoxyadenosines and Their 2', 3'-O-Isopropylidene Derivatives
- Purines. IX. Deoxygenation of 1-Benzyloxyadenine Derivatives : The Formation of Benzaldehyde
- Purines. VII. 1-Alkoxy-9-alkyladenine Salts as Possible Alkylating Reagents