転移リボ核酸の修飾成分
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概要
- 論文の詳細を見る
The modified nucleosides or bases from transfer ribonucleic acids and related compounds are reviewed from an organic chemical standpoint with particular emphasis on the fluorescent minor components of eukaryotic phenylalanine transfer ribonucleic acids (tRANs<SUP>Phe</SUP>). Structural educidations, syntheses, and chemical properties of these unique tricyclic compounds as well as the use of the chemical properties for modifications of yeast tRNA<SUP>Phe</SUP> at the anticodon loop are summarized.
- 社団法人 有機合成化学協会の論文
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関連論文
- 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
- 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
- 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
- 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
- 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
- フェニルアラニン転移リボ核酸超修飾ヌクレオシドの合成をめぐって
- 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
- Improved Synthesis of 3-Methylguanine
- アデニン環の開裂と再閉環
- 3-Methylxanthosine : Synthesis and Acidic Hydrolysis of the Glycosyl Bond
- 転移リボ核酸微量成分の合成化学的研究
- 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)
- 転移リボ核酸の修飾成分
- 3-Methylinosine
- 不老不死の薬(薬学第二世紀の出発点に立って)