Morris J. Robins - Publications

Affiliations: 
1969-1986 University of Alberta, Edmonton, Alberta, Canada 
 1987- Brigham Young University, Provo, UT, United States 
Website:
http://magazine-dev.byu.edu/morris-j-robins-j-rex-goates-professor-of-chemistry/

153 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Wnuk SF, Mudgal MM, Nowak I, Robins MJ. Model Substrate/Inactivation Reactions for MoaA and Ribonucleotide Reductases: Loss of Bromo, Chloro, or Tosylate Groups from C2 of 1,5-Dideoxyhomoribofuranoses upon Generation of an α-Oxy Radical at C3. Molecules (Basel, Switzerland). 25. PMID 32486052 DOI: 10.3390/Molecules25112539  0.6
2015 Barakat KH, Anwar-Mohamed A, Tuszynski JA, Robins MJ, Tyrrell DL, Houghton M. A Refined Model of the HCV NS5A protein bound to daclatasvir explains drug-resistant mutations and activity against divergent genotypes. Journal of Chemical Information and Modeling. 55: 362-73. PMID 24730573 DOI: 10.1021/Ci400631N  1
2014 Rayala R, Theard P, Ortiz H, Yao S, Young JD, Balzarini J, Robins MJ, Wnuk SF. Synthesis of purine and 7-deazapurine nucleoside analogues of 6-N-(4-Nitrobenzyl)adenosine; inhibition of nucleoside transport and proliferation of cancer cells. Chemmedchem. 9: 2186-92. PMID 24788480 DOI: 10.1002/Cmdc.201402047  1
2012 Balzarini J, Gago F, Kulik W, van Kuilenburg AB, Karlsson A, Peterson MA, Robins MJ. Introduction of a fluorine atom at C3 of 3-deazauridine shifts its antimetabolic activity from inhibition of CTP synthetase to inhibition of orotidylate decarboxylase, an early event in the de novo pyrimidine nucleotide biosynthesis pathway. The Journal of Biological Chemistry. 287: 30444-54. PMID 22730407 DOI: 10.1074/Jbc.M112.378091  1
2011 Damaraju VL, Smith KM, Mowles D, Nowak I, Karpinski E, Young JD, Robins MJ, Cass CE. Interaction of fused-pyrimidine nucleoside analogs with human concentrative nucleoside transporters: High-affinity inhibitors of human concentrative nucleoside transporter 1. Biochemical Pharmacology. 81: 82-90. PMID 20854794 DOI: 10.1016/J.Bcp.2010.09.009  1
2011 Nowak I, Damaraju VL, Cass CE, Young JD, Robins MJ. Autofluorescent fused-pyrimidine nucleosides: Synthesis and evaluation as permeants and inhibitors of human nucleoside transporters Collection of Czechoslovak Chemical Communications. 76: 1395-1412. DOI: 10.1135/Cccc2011061  1
2010 Robins MJ, Peng Y, Damaraju VL, Mowles D, Barron G, Tackaberry T, Young JD, Cass CE. Improved syntheses of 5'-S-(2-aminoethyl)-6-N-(4-nitrobenzyl)-5'-thioadenosine (SAENTA), analogues, and fluorescent probe conjugates: analysis of cell-surface human equilibrative nucleoside transporter 1 (hENT1) levels for prediction of the antitumor efficacy of gemcitabine. Journal of Medicinal Chemistry. 53: 6040-53. PMID 20718495 DOI: 10.1021/Jm100432W  1
2009 Robins MJ, Yang H, Miranda K, Peterson MA, De Clercq E, Balzarini J. Synthesis and biological evaluation of 3,3-difluoropyridine-2,4(1H,3H)-dione and 3-deaza-3-fluorouracil base and nucleoside derivatives. Journal of Medicinal Chemistry. 52: 3018-27. PMID 19378989 DOI: 10.1021/Jm900203H  1
2008 Cai J, Damaraju VL, Groulx N, Mowles D, Peng Y, Robins MJ, Cass CE, Gros P. Two distinct molecular mechanisms underlying cytarabine resistance in human leukemic cells. Cancer Research. 68: 2349-57. PMID 18381442 DOI: 10.1158/0008-5472.Can-07-5528  1
2007 Robins MJ, Nowak I, Wnuk SF, Hansske F, Madej D. Deoxygenative [1,2]-hydride shift rearrangements in nucleoside and sugar chemistry: analogy with the [1,2]-electron shift in the deoxygenation of ribonucleotides by ribonucleotide reductases. The Journal of Organic Chemistry. 72: 8216-21. PMID 17918996 DOI: 10.1021/Jo071102B  1
2007 Robins MJ, Nowak I, Rajwanshi VK, Miranda K, Cannon JF, Peterson MA, Andrei G, Snoeck R, De Clercq E, Balzarini J. Synthesis and antiviral evaluation of 6-(alkyl-heteroaryl)furo[2,3-d]pyrimidin-2(3H)-one nucleosides and analogues with ethynyl, ethenyl, and ethyl spacers at C6 of the furopyrimidine core. Journal of Medicinal Chemistry. 50: 3897-905. PMID 17622128 DOI: 10.1021/Jm070210N  1
2007 Liu J, Robins MJ. S(N)Ar displacements with 6-(fluoro, chloro, bromo, iodo, and alkylsulfonyl)purine nucleosides: synthesis, kinetics, and mechanism1. Journal of the American Chemical Society. 129: 5962-8. PMID 17439120 DOI: 10.1021/Ja070021U  1
2007 Nowak I, Robins MJ. Synthesis of 3'-deoxynucleosides with 2-oxabicyclo[3.1.0]hexane sugar moieties: addition of difluorocarbene to a 3',4'-unsaturated uridine derivative and 1,2-dihydrofurans derived from D- and L-xylose1. The Journal of Organic Chemistry. 72: 3319-25. PMID 17385920 DOI: 10.1021/Jo062614D  1
2007 Visser F, Sun L, Damaraju V, Tackaberry T, Peng Y, Robins MJ, Baldwin SA, Young JD, Cass CE. Residues 334 and 338 in transmembrane segment 8 of human equilibrative nucleoside transporter 1 are important determinants of inhibitor sensitivity, protein folding, and catalytic turnover. The Journal of Biological Chemistry. 282: 14148-57. PMID 17379602 DOI: 10.1074/Jbc.M701735200  1
2007 Nowak I, Robins MJ. Trifluoromethylation of alkenyl bromides and iodides (including 5-iodouracils) with (CF3)2Hg and Cu ("trifluoromethylcopper"). The Journal of Organic Chemistry. 72: 2678-81. PMID 17335236 DOI: 10.1021/Jo062544A  1
2007 Nowak I, Cannon JF, Robins MJ. Addition of difluorocarbene to 3',4'-unsaturated nucleosides: synthesis of 2'-deoxy analogues with a 2-oxabicyclo[3.1.0]hexane framework. The Journal of Organic Chemistry. 72: 532-7. PMID 17221971 DOI: 10.1021/Jo061965P  1
2006 Zhong M, Robins MJ. Regiospecific N9 alkylation of 6-(heteroaryl)purines: shielding of N7 by a proximal heteroaryl C-H1. The Journal of Organic Chemistry. 71: 8901-6. PMID 17081021 DOI: 10.1021/Jo061759H  1
2006 Nowak I, Robins MJ. Addition of difluorocarbene to 4',5'-unsaturated nucleosides: synthesis and deoxygenation reactions of difluorospirocyclopropane nucleosides. The Journal of Organic Chemistry. 71: 8876-83. PMID 17081018 DOI: 10.1021/Jo061606U  1
2006 Zhong M, Nowak I, Robins MJ. Regiospecific and highly stereoselective coupling of 6-(substituted-imidazol-1-yl)purines with 2-deoxy-3,5-di-O-(p-toluoyl)-alpha-D-erythro-pentofuranosyl chloride. Sodium-salt glycosylation in binary solvent mixtures: improved synthesis of cladribine. The Journal of Organic Chemistry. 71: 7773-9. PMID 16995685 DOI: 10.1021/Jo061282+  1
2006 Nowak I, Cannon JF, Robins MJ. N-oxides of adenosine-type nucleosides undergo pyrimidine ring opening and closure to give 5-amino-4-(1,2,4-oxadiazol-3-yl)imidazole derivatives. Organic Letters. 8: 4565-8. PMID 16986951 DOI: 10.1021/Ol061715V  1
2006 Zhang J, Smith KM, Tackaberry T, Sun X, Carpenter P, Slugoski MD, Robins MJ, Nielsen LP, Nowak I, Baldwin SA, Young JD, Cass CE. Characterization of the transport mechanism and permeant binding profile of the uridine permease Fui1p of Saccharomyces cerevisiae. The Journal of Biological Chemistry. 281: 28210-21. PMID 16854981 DOI: 10.1074/Jbc.M605129200  1
2006 Zhong M, Nowak I, Cannon JF, Robins MJ. Structure and synthesis of 6-(substituted-imidazol-1-yl)purines: versatile substrates for regiospecific alkylation and glycosylation at N9. The Journal of Organic Chemistry. 71: 4216-21. PMID 16709063 DOI: 10.1021/Jo060340O  1
2006 Wnuk SF, Robins MJ. Ribonucleotide reductase inhibitors as anti-herpes agents. Antiviral Research. 71: 122-6. PMID 16621038 DOI: 10.1016/J.Antiviral.2006.03.002  1
2006 Nowak I, Jones CT, Robins MJ. Selective removal of the 2'- and 3'-O-acyl groups from 2',3',5'-tri-O-acylribonucleoside derivatives with lithium trifluoroethoxide. The Journal of Organic Chemistry. 71: 3077-81. PMID 16599602 DOI: 10.1021/Jo0600104  1
2006 Zhang J, Sun X, Smith KM, Visser F, Carpenter P, Barron G, Peng Y, Robins MJ, Baldwin SA, Young JD, Cass CE. Studies of nucleoside transporters using novel autofluorescent nucleoside probes. Biochemistry. 45: 1087-98. PMID 16430205 DOI: 10.1021/Bi0520535  1
2006 Robins MJ, Miranda K, Rajwanshi VK, Peterson MA, Andrei G, Snoeck R, De Clercq E, Balzarini J. Synthesis and biological evaluation of 6-(alkyn-1-yl)furo[2,3-d]pyrimidin-2(3H)-one base and nucleoside derivatives. Journal of Medicinal Chemistry. 49: 391-8. PMID 16392824 DOI: 10.1021/Jm050867D  1
2006 Janeba Z, Maklad N, Robins MJ. Synthesis of 6-(alkoxymethyl)- and 6-(alkylsulfanylmethyl)furo[2,3-d] pyrimidin-2(3H)-one analogues Canadian Journal of Chemistry. 84: 561-568. DOI: 10.1139/V06-042  1
2006 Janeba Z, Balzarini J, Andrei G, Snoeck R, De Clercq E, Robins MJ. Synthesis and biological evaluation of 5-(alkyn-1-yl)-1-(p-toluenesulfonyl) uracil derivatives Canadian Journal of Chemistry. 84: 580-586. DOI: 10.1139/V06-041  1
2006 Lin X, Robins MJ. Nucleic acid related compounds. 136. Synthesis of 2-amino- and 2,6-diaminopurine derivatives via inverse-electron-demand Diels-Alder reactions Collection of Czechoslovak Chemical Communications. 71: 1029-1041. DOI: 10.1135/Cccc20061029  1
2005 Robins MJ, Wnuk SF. Reduction of ribonucleosides to 2'-deoxyribonucleosides. Current Protocols in Nucleic Acid Chemistry / Edited by Serge L. Beaucage ... [Et Al.]. Unit 1.11. PMID 18428933 DOI: 10.1002/0471142700.Nc0111S21  1
2005 Janeba Z, Maklad N, Robins MJ. An efficient alternative route to 3,6-disubstituted-furo[2,3-d]pyrimidin-2-one analogues. Nucleosides, Nucleotides & Nucleic Acids. 24: 1729-43. PMID 16438044 DOI: 10.1080/10810730500265757  1
2005 Nowak I, Robins MJ. Hydrothermal deamidation of 4-N-acylcytosine nucleoside derivatives: efficient synthesis of uracil nucleoside esters. Organic Letters. 7: 4903-5. PMID 16235918 DOI: 10.1021/Ol0518378  1
2005 Zhong M, Nowak I, Robins MJ. 6-(2-Alkylimidazol-1-yl)purines undergo regiospecific glycosylation at N9. Organic Letters. 7: 4601-3. PMID 16209489 DOI: 10.1021/Ol051573P  1
2005 Nowak I, Conda-Sheridan M, Robins MJ. Nucleic acid related compounds. 127. Selective N-deacylation of N,O-peracylated nucleosides in superheated methanol. The Journal of Organic Chemistry. 70: 7455-8. PMID 16122277 DOI: 10.1021/Jo051256W  1
2005 Janeba Z, Balzarini J, Andrei G, Snoeck R, De Clercq E, Robins MJ. Synthesis and biological evaluation of acyclic 3-[(2-hydroxyethoxy)methyl] analogues of antiviral furo- and pyrrolo[2,3-d]pyrimidine nucleosides. Journal of Medicinal Chemistry. 48: 4690-6. PMID 16000005 DOI: 10.1021/Jm050291S  1
2005 Zhang J, Smith KM, Tackaberry T, Visser F, Robins MJ, Nielsen LP, Nowak I, Karpinski E, Baldwin SA, Young JD, Cass CE. Uridine binding and transportability determinants of human concentrative nucleoside transporters. Molecular Pharmacology. 68: 830-9. PMID 15955867 DOI: 10.1124/Mol.105.012187  1
2005 Liu J, Robins MJ. Fluoro, alkylsulfanyl, and alkylsulfonyl leaving groups in suzuki cross-coupling reactions of purine 2'-deoxynucleosides and nucleosides. Organic Letters. 7: 1149-51. PMID 15760161 DOI: 10.1021/Ol050063S  1
2005 Nowak I, Robins MJ. New methodology for the deoxygenative difluoromethylenation of aldehydes and ketones; unexpected formation of tetrafluorocyclopropanes. Organic Letters. 7: 721-4. PMID 15704934 DOI: 10.1021/Ol047416S  1
2004 Nowak I, Cannon JF, Robins MJ. Synthesis and properties of gem-(difluorocyclopropyl)amine derivatives of bicyclo[n.1.0]alkanes. Organic Letters. 6: 4767-70. PMID 15575681 DOI: 10.1021/Ol047943B  1
2004 Liu J, Robins MJ. Azoles as Suzuki cross-coupling leaving groups: syntheses of 6-arylpurine 2'-deoxynucleosides and nucleosides from 6-(imidazol-1-yl)- and 6-(1,2,4-triazol-4-yl)purine derivatives. Organic Letters. 6: 3421-3. PMID 15355067 DOI: 10.1021/Ol048490D  1
2004 Liu J, Janeba Z, Robins MJ. SNAr iodination of 6-chloropurine nucleosides: aromatic Finkelstein reactions at temperatures below -40 degrees C. Organic Letters. 6: 2917-9. PMID 15330647 DOI: 10.1021/Ol048987N  1
2004 Vickers MF, Zhang J, Visser F, Tackaberry T, Robins MJ, Nielsen LP, Nowak I, Baldwin SA, Young JD, Cass CE. Uridine recognition motifs of human equilibrative nucleoside transporters 1 and 2 produced in Saccharomyces cerevisiae. Nucleosides, Nucleotides & Nucleic Acids. 23: 361-73. PMID 15043160 DOI: 10.1081/Ncn-120028333  1
2004 Janeba Z, Lin X, Robins MJ. Functionalization of guanosine and 2'-deoxyguanosine at C6: a modified Appel process and S(N)Ar displacement of imidazole. Nucleosides, Nucleotides & Nucleic Acids. 23: 137-47. PMID 15043142 DOI: 10.1081/Ncn-120027823  1
2003 Zhang J, Visser F, Vickers MF, Lang T, Robins MJ, Nielsen LP, Nowak I, Baldwin SA, Young JD, Cass CE. Uridine binding motifs of human concentrative nucleoside transporters 1 and 3 produced in Saccharomyces cerevisiae. Molecular Pharmacology. 64: 1512-20. PMID 14645682 DOI: 10.1124/Mol.64.6.1512  1
2003 Robins MJ. Ribonucleotide reductases: radical chemistry and inhibition at the active site. Nucleosides, Nucleotides & Nucleic Acids. 22: 519-34. PMID 14565227 DOI: 10.1081/Ncn-120021952  1
2003 Nowak I, Robins MJ. Protection of the amino group of adenosine and guanosine derivatives by elaboration into a 2,5-dimethylpyrrole moiety. Organic Letters. 5: 3345-8. PMID 12943423 DOI: 10.1021/Ol035264F  1
2003 Janeba Z, Francom P, Robins MJ. Efficient syntheses of 2-chloro-2'-deoxyadenosine (cladribine) from 2'-deoxyguanosine(1). The Journal of Organic Chemistry. 68: 989-92. PMID 12558425 DOI: 10.1021/Jo020644K  1
2003 Francom P, Robins MJ. Nucleic acid related compounds. 118. Nonaqueous diazotization of aminopurine derivatives. Convenient access to 6-halo- and 2,6-dihalopurine nucleosides and 2'-deoxynucleosides with acyl or silyl halides. The Journal of Organic Chemistry. 68: 666-9. PMID 12530909 DOI: 10.1021/Jo020625A  1
2003 Zhong M, Robins MJ. Regioisomers in Vorbrüggen's guanine nucleoside synthesis; N9 selectivity with a glucosamine derivative and 2-N-acetyl-6-O- diphenylcarbamoylguanine Tetrahedron Letters. 44: 9327-9330. DOI: 10.1016/J.Tetlet.2003.10.070  1
2002 Wnuk SF, Companioni DR, Neschadimenko V, Robins MJ. The beta-fluorine effect. Electronic versus steric effects in radical deoxygenations of fluorine-containing pentofuranose nucleosides. The Journal of Organic Chemistry. 67: 8794-7. PMID 12467391 DOI: 10.1021/Jo020428B  1
2002 Miles RW, Nielsen LP, Ewing GJ, Yin D, Borchardt RT, Robins MJ. S-homoadenosyl-L-cysteine and S-homoadenosyl-L-homocysteine. Synthesis and binding studies of hon-hydrolyzed substrate analogues with S-adenosyl-L-homocysteine hydrolase. The Journal of Organic Chemistry. 67: 8258-60. PMID 12423165 DOI: 10.1021/Jo020478G  1
2002 Francom P, Janeba Z, Shibuya S, Robins MJ. Nucleic acid related compounds. 116. Nonaqueous diazotization of aminopurine nucleosides. Mechanistic considerations and efficient procedures with tert-butyl nitrite or sodium nitrite. The Journal of Organic Chemistry. 67: 6788-96. PMID 12227811 DOI: 10.1021/Jo0204101  1
2002 Wnuk SF, Chowdhury SM, Garcia PI, Robins MJ. Stereodefined synthesis of O3'-labeled uracil nucleosides. 3'-[(17)O]-2'-Azido-2'-deoxyuridine 5'-diphosphate as a probe for the mechanism of inactivation of ribonucleotide reductases. The Journal of Organic Chemistry. 67: 1816-9. PMID 11895397 DOI: 10.1021/Jo010899I  1
2001 Robins MJ, Miles RW, Samano MC, Kaspar RL. Syntheses of puromycin from adenosine and 7-deazapuromycin from tubercidin, and biological comparisons of the 7-aza/deaza pair. The Journal of Organic Chemistry. 66: 8204-10. PMID 11722226 DOI: 10.1021/Jo010935D  1
2001 Robins MJ, Wilson JS, Madej D, Tyrrell DLJ, Gati WP, Lindmark RJ, Wnuk SF. Nucleic acid related compounds. 114. Synthesis of 2,6-(disubstituted)purine 2′,3′-dideoxynucleosides and selected cytotoxic, anti-hepatitis B, and adenosine deaminase substrate activities Journal of Heterocyclic Chemistry. 38: 1297-1306. DOI: 10.1002/Jhet.5570380609  1
2000 Yang X, Yin D, Wnuk SF, Robins MJ, Borchardt RT. Mechanisms of inactivation of human S-adenosylhomocysteine hydrolase by 5',5',6',6'-tetradehydro-6'-deoxy-6'-halohomoadenosines. Biochemistry. 39: 15234-41. PMID 11106503 DOI: 10.1021/Bi0015055  1
2000 Lin X, Robins MJ. Mild and efficient functionalization at C6 of purine 2'-deoxynucleosides and ribonucleosides. Organic Letters. 2: 3497-9. PMID 11082018 DOI: 10.1021/Ol000255H  1
2000 Robins MJ, Doboszewski B, Timoshchuk VA, Peterson MA. Glucose-derived 3'-(carboxymethyl)-3'-deoxyribonucleosides and 2', 3'-lactones as synthetic precursors for amide-linked oligonucleotide analogues. The Journal of Organic Chemistry. 65: 2939-45. PMID 10814181 DOI: 10.1021/Jo991399G  1
2000 Robins MJ, Doboszewski B, Nilsson BL, Peterson MA. Synthesis of amide-linked [(3')CH2CO-NH(5')] nucleoside analogues of small oligonucleotides. Nucleosides, Nucleotides & Nucleic Acids. 19: 69-86. PMID 10772703 DOI: 10.1080/15257770008032997  1
2000 Wnuk SF, Valdez CA, Khan J, Moutinho P, Robins MJ, Yang X, Borchardt RT, Balzarini J, De Clercq E. Doubly homologated dihalovinyl and acetylene analogues of adenosine: synthesis, interaction with S-adenosyl-L-homocysteine hydrolase, and antiviral and cytostatic effects. Journal of Medicinal Chemistry. 43: 1180-6. PMID 10737751 DOI: 10.1021/Jm990486Y  1
2000 Kumarasinghe ES, Peterson MA, Robins MJ. Synthesis of 5,6-bis(alkyn-1-yl)pyrimidines and related nucleosides Tetrahedron Letters. 41: 8741-8745. DOI: 10.1016/S0040-4039(00)01566-5  1
2000 Lin X, Robins MJ. Mild and efficient functionalization at C6 of purine 2′-deoxynucleosides and ribonucleosides Organic Letters. 2: 3497-3499.  1
1999 Peterson MA, Nilsson BL, Sarker S, Doboszewski B, Zhang W, Robins MJ. Amide-Linked Ribonucleoside Dimers Derived from 5'-Amino-5'-deoxy- and 3'-(Carboxymethyl)-3'-deoxynucleoside Precursors(1). The Journal of Organic Chemistry. 64: 8183-8192. PMID 11674735 DOI: 10.1021/Jo9908647  1
1999 Giziewicz J, Wnuk SF, Robins MJ. Nucleic Acid Related Compounds. 107. Efficient Nitration of Uracil Base and Nucleoside Derivatives(1). The Journal of Organic Chemistry. 64: 2149-2151. PMID 11674318 DOI: 10.1021/Jo9822939  1
1999 Robins MJ. Mechanism-based inhibition of ribonucleotide reductases: new mechanistic considerations and promising biological applications. Nucleosides & Nucleotides. 18: 779-93. PMID 10432680 DOI: 10.1080/15257779908041565  1
1999 Lawrence CC, Gerfen GJ, Samano V, Nitsche R, Robins MJ, Rétey J, Stubbe J. Binding of Cob(II)alamin to the adenosylcobalamin-dependent ribonucleotide reductase from Lactobacillus leichmannii. Identification of dimethylbenzimidazole as the axial ligand. The Journal of Biological Chemistry. 274: 7039-42. PMID 10066759 DOI: 10.1074/Jbc.274.11.7039  1
1999 Yuan CS, Saso Y, Lazarides E, Borchardt RT, Robins MJ. Recent advances in S-adenosyl-L-homocysteine hydrolase inhibitors and their potential clinical applications Expert Opinion On Therapeutic Patents. 9: 1197-1206. DOI: 10.1517/13543776.9.9.1197  1
1999 Wnuk SF, Yuan CS, Borchardt RT, Robins MJ. Design and biological evaluation of new mechanism-based inhibitors of S- adenosyl-L-homocysteine hydrolase Nucleosides and Nucleotides. 18: 595-596. DOI: 10.1080/15257779908041506  1
1999 Robins MJ, Ewing GJ. Biomimetic modeling of the first substrate reaction at the active site of ribonucleotide reductases. Abstraction of H3' by a thiyl free radical Journal of the American Chemical Society. 121: 5823-5824. DOI: 10.1021/Ja984399R  1
1999 Robins MJ, Guo Z, Samano MC, Wnuk SF. Biomimetic simulation of free radical-initiated cascade reactions postulated to occur at the active site of ribonucleotide reductases Journal of the American Chemical Society. 121: X-1432. DOI: 10.1021/Ja983449P  1
1999 Guo Z, Samano MC, Krzykawski JW, Wnuk SF, Ewing GJ, Robins MJ. Biomimetic modeling of the abstraction of H3' by ribonucleotide reductases. 1,5-Hydrogen atom transfer of H3 to aminyl and oxyl, but not thlyl, free radicals in homoribofuranose derivatives Tetrahedron. 55: 5705-5718. DOI: 10.1016/S0040-4020(99)00238-0  1
1999 Ewing GJ, Robins MJ. An efficient one-stage deprotection/reduction of 1,2-O-isopropylidene furanoses to the corresponding tetrahydrofurans Organic Letters. 1: 635-636.  1
1998 Maeba I, Morishita N, Francom P, Robins MJ. Synthesis of (S)-5-(4,5-Dihydroxypentyl)uracil from Pseudouridine and Clarification of Stereochemistry(1). The Journal of Organic Chemistry. 63: 7539-7541. PMID 11672413 DOI: 10.1021/Jo980975Q  1
1998 Robins MJ, Lewandowska E, Wnuk SF. Nucleic Acid Related Compounds. 105. Synthesis of 2',3'-Didehydro-2',3'-dideoxynucleosides from Ribonucleoside Cyclic 2',3'-(Sulfates or Phosphates) or 2',3'-Dimesylates via Reductive Elimination with Sodium Naphthalenide(1). The Journal of Organic Chemistry. 63: 7375-7381. PMID 11672386 DOI: 10.1021/Jo981013M  0.56
1998 Robins MJ, Wnuk SF, Yang X, Yuan CS, Borchardt RT, Balzarini J, De Clercq E. Inactivation of S-adenosyl-L-homocysteine hydrolase and antiviral activity with 5',5',6',6'-tetradehydro-6'-deoxy-6'-halohomoadenosine analogues (4'-haloacetylene analogues derived from adenosine). Journal of Medicinal Chemistry. 41: 3857-64. PMID 9748360 DOI: 10.1021/Jm980163M  1
1998 Wnuk SF, Yuan CS, Borchardt RT, Robins MJ. Synthesis of homologated halovinyl derivatives from aristeromycin and their inhibition of human placental S-adenosyl-L-homocysteine hydrolase. Nucleosides & Nucleotides. 17: 99-113. PMID 9708344 DOI: 10.1080/07328319808005161  1
1998 Wnuk SF, Mao Y, Yuan CS, Borchardt RT, Andrei G, Balzarini J, De Clercq E, Robins MJ. Discovery of type II (covalent) inactivation of S-adenosyl-L-homocysteine hydrolase involving its "hydrolytic activity": synthesis and evaluation of dihalohomovinyl nucleoside analogues derived from adenosine. Journal of Medicinal Chemistry. 41: 3078-83. PMID 9685247 DOI: 10.1021/Jm9801410  1
1998 Yuan CS, Wnuk SF, Robins MJ, Borchardt RT. A novel mechanism-based inhibitor (6'-bromo-5', 6'-didehydro-6'-deoxy-6'-fluorohomoadenosine) that covalently modifies human placental S-adenosylhomocysteine hydrolase. The Journal of Biological Chemistry. 273: 18191-7. PMID 9660780 DOI: 10.1074/Jbc.273.29.18191  1
1998 van der Donk WA, Yu G, Pérez L, Sanchez RJ, Stubbe J, Samano V, Robins MJ. Detection of a new substrate-derived radical during inactivation of ribonucleotide reductase from Escherichia coli by gemcitabine 5'-diphosphate. Biochemistry. 37: 6419-26. PMID 9572859 DOI: 10.1021/Bi9729357  1
1998 Silva DJ, Stubbe J, Samano V, Robins MJ. Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation. Biochemistry. 37: 5528-35. PMID 9548936 DOI: 10.1021/Bi972934E  1
1998 Robins MJ, Sarker S, Wnuk SF. What are the practical limits for detection of minor nucleoside reaction products with HPLC (UV detection), 1H NMR, and TLC (UV detection)? Nucleosides and Nucleotides. 17: 785-790. DOI: 10.1080/07328319808004675  1
1998 Robins MJ, Lewandowska E, Wnuk SF. Nucleic acid related compounds. 105. Synthesis of 2',3'-didehydro- 2',3'-dideoxynucleosides from ribonucleoside cyclic 2',3'-(Sulfates or phosphates) or 2',3'-dimesylates via reductive elimination with sodium naphthalenide Journal of Organic Chemistry. 63: 7375-7381. DOI: 10.1021/jo981013m  1
1998 Robins MJ, Neschadimenko V, Ro B, Yuan C, Borchardt RT, Wnuk SF. Nucleic Acid Related Compounds. 101.S-Adenosyl-l-homocysteine Hydrolase Does Not Hydrate (5‘-Fluoro)vinyl or (6‘-Halo)homovinyl Analogues Derived from 3‘-Deoxyadenosine or 3‘-(Chloro or Fluoro)-3‘-deoxyadenosine1 Journal of Organic Chemistry. 63: 1205-1211. DOI: 10.1021/Jo971741U  0.56
1998 Robins MJ, Neschadimenko V, Ro BO, Yuan CS, Borchardt RT, Wnuk SF. Nucleic Acid Related Compounds. 101. S-Adenosyl-L-homocysteine Hydrolase Does Not Hydrate (5′-Fluoro)vinyl or (6′-Halo)homovinyl Analogues Derived from 3′-Deoxyadenosine or 3′-(Chloro or Fluoro)-3′-deoxyadenosine Journal of Organic Chemistry. 63: 1205-1211.  1
1997 Huang H, Yuan CS, Wnuk SF, Robins MJ, Borchardt RT. The mechanism of inactivation of human placental S-adenosylhomocysteine hydrolase by (E)-4',5'-didehydro-5'-methoxyadenosine and adenosine 5'-carboxaldehyde oxime. Archives of Biochemistry and Biophysics. 343: 109-17. PMID 9210652 DOI: 10.1006/Abbi.1997.0159  1
1997 Wnuk SF, Yuan CS, Borchardt RT, Balzarini J, De Clercq E, Robins MJ. Anticancer and antiviral effects and inactivation of S-adenosyl-L-homocysteine hydrolase with 5'-carboxaldehydes and oximes synthesized from adenosine and sugar-modified analogues. Journal of Medicinal Chemistry. 40: 1608-18. PMID 9171871 DOI: 10.1021/Jm960828P  1
1997 Robins MJ, Zou R, Hansske F, Wnuk SF. Synthesis of sugar-modified 2,6-diaminopurine and guanine nucleosides from guanosine via transformations of 2-aminoadenosine and enzymatic deamination with adenosine deaminase Canadian Journal of Chemistry. 75: 762-767. DOI: 10.1139/V97-092  1
1997 Robins MJ, Guo Z, Wnuk SF. Elimination of chlorine (radical) or tosylate (anion) from C2' of nucleoside C3' free radicals as model reactions postulated to occur at the active site of ribonucleotide reductases Journal of the American Chemical Society. 119: 3637-3638. DOI: 10.1021/Ja970171C  1
1997 Ashley GW, Lawrence CC, Stubbe J, Robins MJ. Mechanism based inactivation of the adenosylcobalamin-dependent ribonucleotide reductase from L. leichmannii by 2'-ara-2'-azido-2'-deoxy adenosine-5'-triphosphate: Observation of paramagnetic intermediates Tetrahedron. 53: 12005-12016. DOI: 10.1016/S0040-4020(97)00713-8  1
1997 Lewandowska E, Neschadimenko V, Wnuk SF, Robins MJ. Efficient removal of sugar O-tosyl groups and heterocycle halogens from purine nucleosides with sodium naphthalenide Tetrahedron. 53: 6295-6302. DOI: 10.1016/S0040-4020(97)00313-X  1
1997 Robins MJ, Sarker S, Samano V, Wnuk SF. Nucleic acid related compounds. 94. Remarkably high stereoselective reductions of 2'- and 3'-ketonucleoside derivatives to give arabino, ribo, and xylofuranosyl nucleosides with hydrogen isotopes at C2' and C3' Tetrahedron. 53: 447-456. DOI: 10.1016/S0040-4020(96)01035-6  1
1997 Yuan CS, Wnuk SF, Robins MJ, Borchardt RT. A novel mechanism-based inhibitor (6'-bromo-5',6'-didehydro-6'deoxy-6'- fluorohomoadenosine) that covalently modifies human placental s-adenosylhomocysteine hydrolase Faseb Journal. 11: A1019.  1
1996 Wnuk SF, Liu S, Yuan CS, Borchardt RT, Robins MJ. Inactivation of S-adenosyl-L-homocysteine hydrolase by amide and ester derivatives of adenosine-5'-carboxylic acid. Journal of Medicinal Chemistry. 39: 4162-6. PMID 8863793 DOI: 10.1021/Jm960313Y  1
1996 Howe AY, Robins MJ, Wilson JS, Tyrrell DL. Selective inhibition of the reverse transcription of duck hepatitis B virus by binding of 2',3'-dideoxyguanosine 5'-triphosphate to the viral polymerase. Hepatology (Baltimore, Md.). 23: 87-96. PMID 8550054 DOI: 10.1002/hep.510230113  1
1996 Robins MJ, Zou R, Guo Z, Wnuk SF. Nucleic acid related compounds. 93. A solution for the historic problem of regioselective sugar-base coupling to produce 9-glycosylguanines or 7-glycosylguanines Journal of Organic Chemistry. 61: 9207-9212. DOI: 10.1021/Jo9617023  1
1996 Xie M, Berges DA, Robins MJ. Efficient "dehomologation" of di-O-isopropylidenehexofuranose derivatives to give O-isopropylidenepentofuranoses by sequential treatment with periodic acid in ethyl acetate and sodium borohydride Journal of Organic Chemistry. 61: 5178-5179. DOI: 10.1021/Jo960355U  1
1996 Robins MJ, Guo Z, Samano MC, Wnuk SF. Biomimetic modeling of the decomposition of 2'-chloro-2'-deoxynucleotides by ribonucleotide reductases to give 3(2H)-furanones which can effect mechanism-based inactivation by Michael-type alkylation Journal of the American Chemical Society. 118: 11317-11318. DOI: 10.1021/Ja962118E  1
1996 Robins MJ, Wnuk SF, Hernández-Thirring AE, Samano MC. Nucleic acid related compounds. 91. Biomimetic reactions are in harmony with loss of 2'-substituents as free radicals (not anions) during mechanism-based inactivation of ribonucleotide reductases. Differential interactions of azide, halogen, and alkylthio groups with tributylstannane and triphenylsilane Journal of the American Chemical Society. 118: 11341-11348. DOI: 10.1021/Ja962117M  1
1996 Yuan CS, Liu S, Wnuk SF, Robins MJ, Borchardt RT. Design and synthesis of S-adenosylhomocysteine hydrolase inhibitors as broad-spectrum antiviral agents Advances in Antiviral Drug Design. 2: 41-88. DOI: 10.1016/S1075-8593(96)80103-1  1
1996 Robins MJ, Sarker S, Xie M, Zhang W, Peterson MA. Synthesis of 2',3'-fused (3.3.0) γ-butyrolactone-nucleosides and coupling with amino-nucleosides to give amide-linked nucleotide-dimer analogues Tetrahedron Letters. 37: 3921-3924. DOI: 10.1016/0040-4039(96)00715-0  1
1996 Asakura JI, Robins MJ, Asaka Y, Kirn TH. Removal of acetal, silyl, and 4, 4′-dimethoxytrityl protecting groups from hydroxyl functions of carbohydrates and nucleosides with clay in aqueous methanol Journal of Organic Chemistry. 61: 9026-9027.  1
1996 Van Der Donk W, Licht S, Da Salva D, McCarthy J, Robins MJ, Stubbe J. Ribonucleotide reductase: no longer confusing but still amazing Faseb Journal. 10: A1086.  1
1996 Huang H, Yuan CS, Borcliardt RT, Wnuk SF, Robins MJ. The mechanisms of inactivation of human placental S-adenosylhomocysteine hydrolase by (£)-4',5'-didehydro-5'-methoxyadenosine (DMOA) and adenosine 5'-cartaxaldehyde oxime (ACAO) Faseb Journal. 10: A1244.  1
1994 Yuan CS, Liu S, Wnuk SF, Robins MJ, Borchardt RT. Mechanism of inactivation of S-adenosylhomocysteine hydrolase by (E)-5',6'-didehydro-6'-deoxy-6'-halohomoadenosines. Biochemistry. 33: 3758-65. PMID 8142376 DOI: 10.1021/Bi00178A036  0.56
1994 Wnuk SF, Yuan CS, Borchardt RT, Balzarini J, De Clercq E, Robins MJ. Nucleic acid related compounds. 84. Synthesis of 6'-(E and Z)-halohomovinyl derivatives of adenosine, inactivation of S-adenosyl-L-homocysteine hydrolase, and correlation of anticancer and antiviral potencies with enzyme inhibition. Journal of Medicinal Chemistry. 37: 3579-87. PMID 7932585 DOI: 10.1021/Jm00047A015  0.56
1994 Yuan CS, Wnuk SF, Liu S, Robins MJ, Borchardt RT. (E)-5',6'-didehydro-6'-deoxy-6'-fluorohomoadenosine: a substrate that measures the hydrolytic activity of S-adenosylhomocysteine hydrolase. Biochemistry. 33: 12305-11. PMID 7918452 DOI: 10.1021/Bi00206A038  0.56
1994 Buolamwini JK, Craik JD, Wiley JS, Robins MJ, Gati WP, Cass CE, Paterson ARP. Conjugates of fluorescein and SAENTA (5'-S-(2-aminoethyl)-N6-(4- nitrobenzyl)-5'-thioadenosine): Flow cytometry probes for the es nucleoside transporter elements of the plasma membrane Nucleosides and Nucleotides. 13: 737-751. DOI: 10.1080/15257779408013276  1
1993 Liu S, Wnuk SF, Yuan C, Robins MJ, Borchardt RT. Adenosine-5'-carboxaldehyde: a potent inhibitor of S-adenosyl-L-homocysteine hydrolase. Journal of Medicinal Chemistry. 36: 883-7. PMID 8464042 DOI: 10.1021/Jm00059A013  0.56
1993 Salowe S, Bollinger JM, Ator M, Stubbe J, McCraken J, Peisach J, Samano MC, Robins MJ. Alternative model for mechanism-based inhibition of Escherichia coli ribonucleotide reductase by 2'-azido-2'-deoxyuridine 5'-diphosphate. Biochemistry. 32: 12749-60. PMID 8251496 DOI: 10.1021/Bi00210A026  1
1992 Robins MJ, Samano V, Zhang W, Balzarini J, De Clercq E, Borchardt RT, Lee Y, Yuan CS. Nucleic acid related compounds. 74. Synthesis and biological activity of 2'(and 3')-deoxy-2'(and 3')-methylenenucleoside analogues that function as mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase and/or ribonucleotide reductase. Journal of Medicinal Chemistry. 35: 2283-93. PMID 1613752 DOI: 10.1021/Jm00090A020  0.56
1992 Fleming SA, Rawlins DB, Samano V, Robins MJ. Photochemistry of nucleoside transport inhibitor 6-S-benzylated thiopurine ribonucleosides. Implications for a new class of photoaffinity labels Journal of Organic Chemistry. 57: 5968-5976. DOI: 10.1021/Jo00048A034  1
1991 Baker CH, Banzon J, Bollinger JM, Stubbe J, Samano V, Robins MJ, Lippert B, Jarvi E, Resvick R. 2'-Deoxy-2'-methylenecytidine and 2'-deoxy-2',2'-difluorocytidine 5'-diphosphates: potent mechanism-based inhibitors of ribonucleotide reductase. Journal of Medicinal Chemistry. 34: 1879-84. PMID 2061926 DOI: 10.1021/Jm00110A019  1
1991 Wiley JS, Brocklebank AM, Snook MB, Jamieson GP, Sawyer WH, Craik JD, Cass CE, Robins MJ, McAdam DP, Paterson AR. A new fluorescent probe for the equilibrative inhibitor-sensitive nucleoside transporter. 5'-S-(2-aminoethyl)-N6-(4-nitrobenzyl)-5'-thioadenosine (SAENTA)-chi 2-fluorescein. The Biochemical Journal. 273: 667-72. PMID 1996965 DOI: 10.1042/Bj2730667  1
1990 Agbanyo FR, Vijayalakshmi D, Craik JD, Gati WP, McAdam DP, Asakura J, Robins MJ, Paterson AR, Cass CE. 5'-S-(2-aminoethyl)-N6-(4-nitrobenzyl)-5'-thioadenosine (SAENTA), a novel ligand with high affinity for polypeptides associated with nucleoside transport. Partial purification of the nitrobenzylthioinosine-binding protein of pig erythrocytes by affinity chromatography. The Biochemical Journal. 270: 605-14. PMID 2241896 DOI: 10.1042/Bj2700605  1
1990 Balzarini J, Naesens L, Robins MJ, De Clercq E. Potentiating effect of ribavirin on the in vitro and in vivo antiretrovirus activities of 2',3'-dideoxyinosine and 2',3'-dideoxy-2,6-diaminopurine riboside. Journal of Acquired Immune Deficiency Syndromes. 3: 1140-7. PMID 2123003  0.36
1990 Fleming SA, Rawlins DB, Robins MJ. Photochemistry of the nucleoside membrane transport inhibitor 6-[(4-nitrobenzyl) thio]-9-(β-D-ribofuranosyl)purine Tetrahedron Letters. 31: 4995-4998. DOI: 10.1016/S0040-4039(00)97787-6  1
1989 Robins MJ, Wood SG, Dalley NK, Herdewijn P, Balzarini J, De Clercq E. Nucleic acid related compounds. 57. Synthesis, x-ray crystal structure, lipophilic partition properties, and antiretroviral activities of anomeric 3'-azido-2',3'-dideoxy-2,6-diaminopurine ribosides. Journal of Medicinal Chemistry. 32: 1763-8. PMID 2754702 DOI: 10.1021/Jm00128A017  0.36
1988 Pauwels R, Baba M, Balzarini J, Herdewijn P, Desmyter J, Robins MJ, Zou RM, Madej D, De Clercq E. Investigations on the anti-HIV activity of 2',3'-dideoxyadenosine analogues with modifications in either the pentose or purine moiety. Potent and selective anti-HIV activity of 2,6-diaminopurine 2',3'-dideoxyriboside. Biochemical Pharmacology. 37: 1317-25. PMID 3258516 DOI: 10.1016/0006-2952(88)90789-7  0.36
1988 Balzarini J, Baba M, Pauwels R, Herdewijn P, Wood SG, Robins MJ, de Clercq E. Potent and selective activity of 3'-azido-2,6-diaminopurine-2',3'-dideoxyriboside, 3'-fluoro-2,6-diaminopurine-2',3'-dideoxyriboside, and 3'-fluoro-2',3'-dideoxyguanosine against human immunodeficiency virus. Molecular Pharmacology. 33: 243-9. PMID 3258404  0.36
1987 De Clercq E, Balzarini J, Madej D, Hansske F, Robins MJ. Nucleic acid related compounds. 51. Synthesis and biological properties of sugar-modified analogues of the nucleoside antibiotics tubercidin, toyocamycin, sangivamycin, and formycin. Journal of Medicinal Chemistry. 30: 481-6. PMID 3820218 DOI: 10.1021/Jm00386A007  0.36
1987 Balzarini J, Robins MJ, Zou RM, Herdewijn P, De Clercq E. The 2',3'-dideoxyriboside of 2,6-diaminopurine and its 2',3'-didehydro derivative inhibit the deamination of 2',3'-dideoxyadenosine, an inhibitor of human immunodeficiency virus (HIV) replication. Biochemical and Biophysical Research Communications. 145: 277-83. PMID 3496090 DOI: 10.1016/0006-291X(87)91317-9  0.36
1987 Balzarini J, Pauwels R, Baba M, Robins MJ, Zou RM, Herdewijn P, De Clercq E. The 2',3'-dideoxyriboside of 2,6-diaminopurine selectively inhibits human immunodeficiency virus (HIV) replication in vitro. Biochemical and Biophysical Research Communications. 145: 269-76. PMID 3496089 DOI: 10.1016/0006-291X(87)91316-7  0.36
1987 Baba M, Pauwels R, Balzarini J, Herdewijn P, Clercq ED, Desmyter J, Robins MJ. The anti-HIV activity of 2$prime;, 3$prime;-dideoxyadenosine analogues Cancer Letters. 36. DOI: 10.1016/0304-3835(87)90240-0  0.36
1986 De Clercq E, Robins MJ. Xylotubercidin against herpes simplex virus type 2 in mice. Antimicrobial Agents and Chemotherapy. 30: 719-24. PMID 3800347 DOI: 10.1128/Aac.30.5.719  0.36
1986 De Clercq E, Bernaerts R, Bergstrom DE, Robins MJ, Montgomery JA, Holy A. Antirhinovirus activity of purine nucleoside analogs. Antimicrobial Agents and Chemotherapy. 29: 482-7. PMID 3013084 DOI: 10.1128/Aac.29.3.482  1
1985 Balzarini J, De Clercq E, Herdewijn P, Robins MJ. Role of thymidine kinase and thymidylate synthetase in the cytostatic, antimetabolic, and antitumor effects of the carbocyclic analogue of 5-nitro-2'-deoxyuridine. A comparison with 5-nitro-2'-deoxyuridine. Molecular Pharmacology. 27: 578-83. PMID 3990680  1
1985 Robins MJ, Hatfield PW, Balzarini J, Clercq ED. Nucleic Acid Related Compounds. 47. Synthesis And Biological Activities Of Pyrimidine And Purine “Acyclic” Nucleoside Analogs Cheminform. 16. DOI: 10.1002/Chin.198512237  0.36
1984 Robins MJ, Hatfield PW, Balzarini J, De Clercq E. Nucleic acid related compounds. 47. Synthesis and biological activities of pyrimidine and purine "acyclic" nucleoside analogues. Journal of Medicinal Chemistry. 27: 1486-92. PMID 6092636 DOI: 10.1021/Jm00377A018  1
1984 Robins MJ, Hansske F, Low NH, Park JI. A mild conversion of vicinal diols to alkenes. Efficient transformation of ribonucleosides into 2′-ene and 2t',3′-dideoxynucleosides Tetrahedron Letters. 25: 367-370. DOI: 10.1016/S0040-4039(00)99885-X  1
1983 De Clercq E, Descamps J, Balzarini J, Giziewicz J, Barr PJ, Robins MJ. Nucleic acid related compounds. 40. Synthesis and biological activities of 5-alkynyluracil nucleosides. Journal of Medicinal Chemistry. 26: 661-6. PMID 6302254 DOI: 10.1002/Chin.198338357  0.36
1976 Robins MJ, Kanai T. Nucleic acid related compounds. 19. Concerning the mechanism of formation of "2,3′-imino-1-(β-D-lyxofuranosyl)uracil" [2-amino-1-(3-deoxy-β-D-lyxofuranosyl)-4-pyrimidinone-N 2→3′-anhydronucleoside] from O2→2′ cyclonucleosides and "ammonium azide" Journal of Organic Chemistry. 41: 1886-1887. PMID 1262996 DOI: 10.1021/Jo00872A051  1
1976 Robins MJ, Jones RA, Mengel R. Nucleic acid related compounds. 23. Transformation of ribonucleoside 2',3'-O-ortho esters into unsaturated and deoxy sugar nucleosides via enol ester-substituted iodo intermediates. Journal of the American Chemical Society. 98: 8213-7. PMID 993520 DOI: 10.1002/Chin.197711363  1
1976 Robins MJ, Mengel R, Jones RA, Fouron Y. Nucleic acid related compounds.22. Transformation of ribonucleoside 2,3'-O-ortho esters into halo, deoxy, and epoxy sugar nucleosides using acyl halides. Mechanism and structure of products. Journal of the American Chemical Society. 98: 8204-13. PMID 993519 DOI: 10.1002/Chin.197710371  1
1974 Robins MJ, Jones RA, MacCoss M. 3'-O-aminoacyl-2'-deoxyadenosines and 2'-O-aminoacyl-3'-deoxyadenosines related to charged transfer ribonucleic acid termini. Biochemistry. 13: 553-9. PMID 4543925 DOI: 10.1021/Bi00700A023  1
1973 Bloch A, Dutschman G, Currie BL, Robins RK, Robins MJ. Preparation and biological activity of various 3-deazapyrimidines and related nucleosides. Journal of Medicinal Chemistry. 16: 294-7. PMID 4200222 DOI: 10.1021/Jm00261A032  1
1971 Miles DW, Townsend LB, Robins MJ, Robins RK, Inskeep WH, Eyring H. Circular dichroism of nucleoside derivatives. X. Influence of solvents and substituents upon the Cotton effects of guanosine derivatives. Journal of the American Chemical Society. 93: 1600-8. PMID 5550248  1
1971 Robins MJ, Simon LN, Stout MG, Ivanovics GA, Schweizer MP, Rousseau RJ, Robins RK. Nucleoside peptides. I. The synthesis of 5'-deoxy-5'-amino-5'-N-aminoacyl peptide derivatives of guanosine, adenosine, and 2'-deoxyadenosine and their effect on cell-free protein synthesis. Journal of the American Chemical Society. 93: 1474-80. PMID 5548345 DOI: 10.1021/Ja00735A025  1
1971 ROBINS MJ, SIMON LN, STOUT MG, IVANOVICS GA, SCHWEIZER MP, ROUSSEAU RJ, ROBINS RK. ChemInform Abstract: NUCLEOSIDPEPTIDE 1. MITT. SYNTHESE VON 5′-N-AMINOACYL-5′-DESOXY-5′-AMINO-DERIVATEN VON GUANOSIN, ADENOSIN UND 2′-DESOXY-ADENOSIN UND IHR EINFLUSS AUF DIE ZELLFREIE PROTEIN-SYNTHESE Chemischer Informationsdienst. Organische Chemie. 2: no-no. DOI: 10.1002/Chin.197125377  0.36
1970 Shuman DA, Robins MJ, Robins RK. The synthesis of nucleos9de sulfamates related to nucleocidin. Journal of the American Chemical Society. 92: 3434-40. PMID 5422764 DOI: 10.1021/Ja00714A035  1
1970 Miles DW, Inskeep WH, Robins MJ, Winkley MW, Robins RK, Eyring H. Circular dichroism of nucleoside derivatives. IX. Vicinal effects on the circular dichroism of pyrimidine nucleosides. Journal of the American Chemical Society. 92: 3872-81. PMID 5419044 DOI: 10.1021/Ja00716A007  1
1970 Robins MJ, Khwaja TA, Robins RK. Purine nucleosides. XXIX. The synthesis of 2'-deoxy-L-adenosine and 2'-deoxy-L-guanosine and their alpha anomers. The Journal of Organic Chemistry. 35: 636-9. PMID 5416936 DOI: 10.1021/Jo00828A019  1
1969 Robins MJ, Robins RK. Purine nucleosides. XXIV. A new method for the synthesis of guanine nucleosides. The preparation of 2'-deoxy-alpha and beta-guanosines and the corresponding N2-methyl derivatives. The Journal of Physical Chemistry. 34: 2160-3. PMID 5788210 DOI: 10.1021/Jo01259A029  1
1969 Miles DW, Robins MJ, Robins RK, Winkley MW, Eyring H. Circular dichroism of nucleoside derivatives. IV. Uracil derivatives. Journal of the American Chemical Society. 91: 824-31. PMID 5781567 DOI: 10.1021/Ja01032A005  1
1969 Miles DW, Robins MJ, Robins RK, Winkley MW, Eyring H. Circular dichroism of nucleoside derivatives. V. Cytosine derivatives. Journal of the American Chemical Society. 91: 831-8. PMID 5778273 DOI: 10.1021/Ja01032A006  1
1969 Miles DW, Robins MJ, Robins RK, Eyring H. Circular dichroism of nucleoside derivatives. VI. The optically active bands of adenine nucleoside derivatives. Proceedings of the National Academy of Sciences of the United States of America. 62: 22-9. PMID 5253660 DOI: 10.1073/Pnas.62.1.22  1
1969 Stout MG, Robins MJ, Olsen RK, Robins RK. Purine nucleosides. XXV. The synthesis of certain derivatives of 5'-amino-5'-deoxy- and 5'-amino-2',5'-dideoxy-beta-d-ribofuranosylpurines as purine nucleotide analogs. Journal of Medicinal Chemistry. 12: 658-62. PMID 4893464 DOI: 10.1021/Jm00304A022  1
1969 Shuman DA, Bloch A, Robins RK, Robins MJ. Synthesis and biological activity of certain 8-mercaptopurine and 6-mercaptopyrimidine S-nucleosides. Journal of Medicinal Chemistry. 12: 653-7. PMID 4893463 DOI: 10.1021/Jm00304A021  1
1968 McCarthy JR, Robins RK, Robins MJ. Purine nucleosides. XXII. The synthesis of angustmycin A (decoyinine) and related unsaturated nucleosides. Journal of the American Chemical Society. 90: 4993-9. PMID 5665542 DOI: 10.1021/Ja01020A038  1
1968 Miles DW, Hahn SJ, Robins RK, Robins MJ, Eyring H. Vicinal effects on the optical activity of some adenine nucleosides. The Journal of Physical Chemistry. 72: 1483-91. PMID 5648867 DOI: 10.1021/J100851A015  1
1967 McCarthy JR, Robins MJ, Robins RK. The synthesis of unsaturated adenine nucleosides related to angustmycin A Chemical Communications (London). 536-537. DOI: 10.1039/C19670000536  1
1966 Robins MJ, McCarthy JR, Robins RK. Purine nucleosides. XII. The preparation of 2',3'-dideoxyadenosine, 2',5'-dideoxyadenosine, and 2',3',5'-trideoxyadenosine from 2'-deoxyadenosine. Biochemistry. 5: 224-31. PMID 5938940 DOI: 10.1021/Bi00865A029  1
1966 McCarthy JR, Robins MJ, Townsend LB, Robins RK. Purine nucleosides. XIV. Unsaturated furanosyl adenine nucleosides prepared via base-catalyzed elimination reactions of 2'-deoxyadenosine derivatives. Journal of the American Chemical Society. 88: 1549-53. PMID 5914527 DOI: 10.1021/Ja00959A043  1
1965 Robins MJ, Robins RK. Purine nucleosides. XI. The synthesis of 2'-deoxy-9-alpha- and-beta-D-ribofuranosylpurines and the correlation of their anomeric structure with proton magnetic resonance spectra. Journal of the American Chemical Society. 87: 4934-40. PMID 5844465 DOI: 10.1021/Ja00949A042  1
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