Total synthesis of malayamycin A and analogues
暂无分享,去创建一个
[1] S. Hanessian,et al. Total synthesis of N-malayamycin A and related bicyclic purine and pyrimidine nucleosides. , 2005, The Journal of organic chemistry.
[2] P. Nielsen,et al. An alpha-D-configured bicyclic nucleoside restricted in an E-type conformation: synthesis and parallel RNA recognition. , 2005, The Journal of organic chemistry.
[3] J. Mcmurry,et al. The Organic Chemistry of Biological Pathways , 2005 .
[4] David R. Liu,et al. DNA-templated organic synthesis: nature's strategy for controlling chemical reactivity applied to synthetic molecules. , 2004, Angewandte Chemie.
[5] C. Simons,et al. Synthetic Methodologies for C-Nucleosides , 2004 .
[6] L. Cartee,et al. Challenges in antimicrobial drug discovery and the potential of nucleoside antibiotics. , 2004, Current medicinal chemistry.
[7] S. Hanessian,et al. A highly stereocontrolled and efficient synthesis of α- and β-pseudouridines , 2003 .
[8] S. Hanessian,et al. Total synthesis and structural confirmation of malayamycin A: a novel bicyclic C-nucleoside from Streptomyces malaysiensis. , 2003, Organic letters.
[9] C. Reese,et al. Conversion of 2-deoxy-D-ribose into 2-amino-5-(2-deoxy-beta-D-ribofuranosyl)pyridine, 2'-deoxypseudouridine, and other C-(2'-deoxyribonucleosides). , 2003, Organic & biomolecular chemistry.
[10] Eric Therrien,et al. Synthesis of diversely functionalized indolizidinones and related bicyclic lactams using intramolecular Grubbs olefin metathesis and Dieckmann condensation. , 2003, The Journal of organic chemistry.
[11] K. Ando,et al. Beta-pseudouridine, a beer component, reduces radiation-induced chromosome aberrations in human lymphocytes. , 2003, Mutation research.
[12] R. Furneaux,et al. Glucofuranosylation with penta-O-propanoyl-β-d-glucofuranose , 2002 .
[13] H. Choo,et al. L-nucleosides: antiviral activity and molecular mechanism. , 2002, Current topics in medicinal chemistry.
[14] R. Hosmane. Ring-expanded ("Fat") nucleosides as broad-spectrum anticancer and antiviral agents. , 2002, Current topics in medicinal chemistry.
[15] T. Hatano,et al. Pseudouridine, an antimutagenic substance in beer towards N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). , 2002, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.
[16] V. Guérineau,et al. Stereocontrolled synthesis of heterocyclic C-nucleosides. Protecting group effect and molecular modeling studies. , 2002, The Journal of organic chemistry.
[17] T. Pathak. Azidonucleosides: synthesis, reactions, and biological properties. , 2002, Chemical reviews.
[18] J. Ofengand. Ribosomal RNA pseudouridines and pseudouridine synthases , 2002, FEBS letters.
[19] A. Bermejo,et al. Semisynthesis of new tetrahydrofuranic alkyl ester and furano-pyrone derivatives as inhibitors of the mitochondrial complex I , 2002 .
[20] K. Chun,et al. A short synthesis of bicyclic sugar pyrimidine nucleosides from C-glycosides , 2001 .
[21] P. Nielsen,et al. Synthesis of bicyclic nucleosides by ring-closing metathesis , 2001 .
[22] C. Simons. Nucleoside Mimetics: Their Chemistry and Biological Properties , 2000 .
[23] A. Mitra,et al. Synthesis of Acyclovir, Ganciclovir and Their Prodrugs: A Review , 2000 .
[24] Robert M. Stroud,et al. The structural basis for tRNA recognition and pseudouridine formation by pseudouridine synthase I , 2000, Nature Structural Biology.
[25] C. Leumann,et al. Nucleic‐Acid Analogs with Restricted Conformational Flexibility in the Sugar‐Phosphate Backbone (`Bicyclo‐DNA'), Part 7, Synthesis and Properties of Oligodeoxynucleotides Containing [(3′S,5′S,6′R)‐6′‐Amino‐2′‐deoxy‐3′,5′‐ethano‐β‐D‐ribofuranosyl]thymine (=(6′R)‐6′‐Amino‐bicyclo‐thymidine) , 1999 .
[26] H. Overkleeft,et al. A convenient route to cis- and trans-fused bicyclic ethers by ruthenium mediated ring-closing metathesis of diene and enyne carbohydrate derivatives , 1999 .
[27] P. Grohar,et al. A practical synthesis of the modified RNA nucleoside pseudouridine , 1999 .
[28] H. Togo,et al. C-Glycosidation Technology With Free Radical Reactions , 1998 .
[29] S. Armstrong. Ring closing diene metathesis in organic synthesis , 1998 .
[30] Robert H. Grubbs,et al. Recent advances in olefin metathesis and its application in organic synthesis , 1998 .
[31] M. Picquet,et al. Cationic ruthenium allenylidene complexes as a new class of performing catalysts for ring closing metathesis , 1998 .
[32] M. Hirama,et al. Convergent synthesis of the trans-fused 6-n-6-6 (n = 7–10) tetracyclic ether system based on a ring-closing metathesis reaction , 1998 .
[33] H. Overkleeft,et al. A NOVEL APPROACH TOWARDS CIS- AND TRANS-FUSED PYRANOPYRANS BASED ON RING-CLOSING METATHESIS REACTION OF CARBOHYDRATE DERIVATIVES , 1997 .
[34] Matthias Schuster,et al. Olefin Metathesis in Organic Chemistry , 1997 .
[35] B. Maden. Eukaryotic ribosomal RNA: Guides to 95 new angles , 1997, Nature.
[36] M. Delgado,et al. Application of the Grubbs Ring-Closure Olefin Metathesis in the Synthesis of Trans-Fused Oxacycles , 1997 .
[37] E. Kool,et al. C-Nucleosides Derived from Simple Aromatic Hydrocarbons , 1997, Synlett : accounts and rapid communications in synthetic organic chemistry.
[38] J Ofengand,et al. Mapping to nucleotide resolution of pseudouridine residues in large subunit ribosomal RNAs from representative eukaryotes, prokaryotes, archaebacteria, mitochondria and chloroplasts. , 1997, Journal of molecular biology.
[39] D. Ströhl,et al. Easy access to C-glycosides from aldonolactones by a Claisen-type chain-extension reaction , 1997 .
[40] J. S. Clark,et al. Enantioselective synthesis of medium-ring sub-units of brevetoxin A by ring-closing metathesis , 1997 .
[41] K. Nicolaou,et al. Olefin Metathesis in Cyclic Ether Formation. Direct Conversion of Olefinic Esters to Cyclic Enol Ethers with Tebbe-Type Reagents , 1996 .
[42] J. Ziller,et al. Synthesis and Applications of RuCl2(CHR‘)(PR3)2: The Influence of the Alkylidene Moiety on Metathesis Activity , 1996 .
[43] D. Levy,et al. The Chemistry of C-Glycosides , 1995 .
[44] S. Knapp. Synthesis of Complex Nucleoside Antibiotics , 1995 .
[45] F. Leeper,et al. Stereocontrolled syntheses of polyhydroxy indolizidines, including 8a-epi-, 6,8a-diepi- and 1,6-diepi-castanospermine, starting from malic acid , 1995 .
[46] M. Sodeoka,et al. Regio- and Stereoselective Functionalization of an Optically Active Tetrahydroindolizine Derivative. Catalytic Asymmetric Syntheses of Lentiginosine, 1,2-Diepilentiginosine, and Gephyrotoxin 209D , 1995 .
[47] M. Postema. C-Glycoside Synthesis , 1995 .
[48] Carlos Jaramillo,et al. Synthesis of the Ezomycin Octosyl Nucleoside , 1994 .
[49] J. Tamura,et al. A new oxidative conversion of carbohydrate benzyl ethers to benzoyl esters with RuCl3-NaIO4. , 1992 .
[50] R. L. Halterman,et al. Evidence for stereoelectronic control in the epoxidation of sterically unbiased 3,3-diarylcyclopentenes , 1992 .
[51] D. Dess,et al. A useful 12-I-5 triacetoxyperiodinane (the Dess-Martin periodinane) for the selective oxidation of primary or secondary alcohols and a variety of related 12-I-5 species , 1991 .
[52] S. Knapp,et al. Nucleoside synthesis from thioglycosides , 1991 .
[53] A. Meyers,et al. Some observations on the validity and generality of the Cieplak stereoelectronic effect , 1989 .
[54] B. Kim,et al. Cyclic sulfates containing acid-sensitive groups and chemoselective hydrolysis of sulfate esters , 1989 .
[55] G. Schulte,et al. Total synthesis of octosyl acid A. Intramolecular Williamson reaction via a cyclic stannylene derivative , 1988 .
[56] H. Robertson,et al. The r.alpha. structures of pyrazine and pyrimidine by the combined analysis of electron diffraction, liquid-crystal NMR, and rotational data , 1988 .
[57] J. Leonard,et al. Total synthesis of specionin-natural product or artifact? , 1987 .
[58] B. Ganem,et al. syn-Stereoselective Epoxidation of Allylic Ethers Using CF3CO3H. , 1986 .
[59] S. Hanessian,et al. "Quantamycin" - a computer-simulated new-generation inhibitor of bacterial ribosomal binding , 1984 .
[60] M. Cichowicz,et al. A facile method for the oxidative removal of benzyl ethers: the oxidation of benzyl ethers to benzoates by ruthenium tetraoxide , 1984 .
[61] D. Dess,et al. Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones , 1983 .
[62] M. Vaultier,et al. Reduction d'azides en amines primaires par une methode generale utilisant la reaction de staudinger , 1983 .
[63] H. Seto,et al. The structures of novel nucleoside antibiotics, miharamycin A and miharamycin B , 1983 .
[64] A. Cieplak. Stereochemistry of Nucleophilic Addition to Cyclohexanone. The Importance of Two-Electron Stabilizing Interactions , 1981 .
[65] R. Ogden,et al. A synthesis of pseudouridine , 1981 .
[66] O. Mitsunobu. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products , 1981 .
[67] C. Cass,et al. Improved antitumor effects in 3'-branched homologues of 2'-deoxythioguanosine. Synthesis and evaluation of thioguanine nucleosides of 2,3-dideoxy-3-(hydroxymethyl)-D-erythro-pentofuranose. , 1979, Journal of medicinal chemistry.
[68] A. Sakurai,et al. Application of carbon‐13 n.m.r. Spectroscopy to the structural investigation of ezomycins , 1977 .
[69] S. Tamura,et al. Isolation and Antimicrobial Activities of Ezomycins B1, B2, C1, C2, D1 and D2 , 1977 .
[70] S. Hanessian,et al. Synthesis of naturally occurring C-nucleosides, their analogs, and functionalized C-glycosyl precursors. , 1976, Advances in carbohydrate chemistry and biochemistry.
[71] S. Tamura,et al. Structures of ezomycins B1, B2, C1, C2, D1, and D2 , 1975 .
[72] P. Crain,et al. Isolation of structure of octosyl acids. Anhydrooctose uronic acid nucleosides , 1975 .
[73] S. Tamura,et al. Structures of ezomycins A1 and A2 , 1975 .
[74] R. Bannard,et al. Cyclohexane compounds. VII. Nucleophilic scission of the stereoisomeric 3-methoxycyclohexene oxides , 1968 .
[75] B. Griffin,et al. The synthesis of oligoribonucleotides. IV. Preparation of dinucleoside phosphates from 2',5'-protected ribonucleoside derivatives. , 1968, Tetrahedron.
[76] R. Bannard,et al. CYCLOHEXANE COMPOUNDS: V. THE REACTION OF 1-METHOXYCYCLOHEXENE-2 WITH AQUEOUS N-BROMOSUCCINIMIDE. THE 1-METHOXY-2-BROMO-3-HYDROXYCYCLOHEXANES , 1965 .
[77] F. Davis,et al. Ribonucleic acids from yeast which contain a fifth nucleotide. , 1957, The Journal of biological chemistry.
[78] WALDO E. COHN,et al. Nucleoside-5′-Phosphates from Ribonucleic Acid , 1951, Nature.
[79] H. Staudinger,et al. Über neue organische Phosphorverbindungen III. Phosphinmethylenderivate und Phosphinimine , 1919 .