| Year |
Citation |
Score |
| 2018 |
Mohan S, Thompson JR, Pinto BM, Bennet AJ. Versatile synthetic route to carbocyclic N-Acetylneuraminic acid and its derivatives Tetrahedron. 74: 5213-5221. DOI: 10.1016/J.Tet.2018.05.065 |
0.337 |
|
| 2016 |
Colombo C, Pinto BM, Bernardi A, Bennet AJ. Synthesis and evaluation of influenza A viral neuraminidase candidate inhibitors based on a bicyclo[3.1.0]hexane scaffold. Organic & Biomolecular Chemistry. 14: 6539-53. PMID 27305457 DOI: 10.1039/C6Ob00999A |
0.346 |
|
| 2016 |
Mahdavi-Amiri Y, Mohan S, Borrelli S, Slowski K, Sanders DA, Pinto BM. Mechanism-based candidate inhibitors of uridine diphosphate galactopyranose mutase (UGM). Carbohydrate Research. 419: 1-7. PMID 26595659 DOI: 10.1016/J.Carres.2015.10.008 |
0.349 |
|
| 2015 |
Kuppala R, Borrelli S, Slowski K, Sanders DA, Ravindranathan Kartha KP, Pinto BM. Synthesis and biological evaluation of nonionic substrate mimics of UDP-Galp as candidate inhibitors of UDP galactopyranose mutase (UGM). Bioorganic & Medicinal Chemistry Letters. 25: 1995-7. PMID 25819094 DOI: 10.1016/J.Bmcl.2015.03.006 |
0.442 |
|
| 2015 |
Shi Y, Ardá A, Pinto BM. Combined molecular dynamics, STD-NMR, and CORCEMA protocol yields structural model for a UDP-galactopyranose mutase-inhibitor complex. Bioorganic & Medicinal Chemistry Letters. 25: 1284-7. PMID 25681227 DOI: 10.1016/J.Bmcl.2015.01.044 |
0.332 |
|
| 2014 |
Lira-Navarrete E, Iglesias-Fernández J, Zandberg WF, Compañón I, Kong Y, Corzana F, Pinto BM, Clausen H, Peregrina JM, Vocadlo DJ, Rovira C, Hurtado-Guerrero R. Substrate-guided front-face reaction revealed by combined structural snapshots and metadynamics for the polypeptide N-acetylgalactosaminyltransferase 2. Angewandte Chemie (International Ed. in English). 53: 8206-10. PMID 24954443 DOI: 10.1002/Anie.201402781 |
0.317 |
|
| 2014 |
Shi Y, Pinto BM. Human lactate dehydrogenase a inhibitors: a molecular dynamics investigation. Plos One. 9: e86365. PMID 24466056 DOI: 10.1371/Journal.Pone.0086365 |
0.306 |
|
| 2014 |
Mohan S, Kerry PS, Bance N, Niikura M, Pinto BM. Serendipitous discovery of a potent influenza virus a neuraminidase inhibitor. Angewandte Chemie (International Ed. in English). 53: 1076-80. PMID 24339250 DOI: 10.1002/Anie.201308142 |
0.358 |
|
| 2014 |
Poulin MB, Shi Y, Protsko C, Dalrymple SA, Sanders DA, Pinto BM, Lowary TL. Specificity of a UDP-GalNAc pyranose-furanose mutase: a potential therapeutic target for Campylobacter jejuni infections. Chembiochem : a European Journal of Chemical Biology. 15: 47-56. PMID 24302429 DOI: 10.1002/Cbic.201300653 |
0.325 |
|
| 2014 |
Mohan S, Eskandari R, Pinto BM. Naturally occurring sulfonium-ion glucosidase inhibitors and their derivatives: a promising class of potential antidiabetic agents. Accounts of Chemical Research. 47: 211-25. PMID 23964564 DOI: 10.1021/Ar400132G |
0.789 |
|
| 2014 |
Wang S, Shen DL, Lafont D, Vercoutter-Edouart AS, Mortuaire M, Shi Y, Maniti O, Girard-Egrot A, Lefebvre T, Pinto BM, Vocadlo D, Vidal S. Design of glycosyltransferase inhibitors targeting human O-GlcNAc transferase (OGT) Medchemcomm. 5: 1172-1178. DOI: 10.1039/C4Md00063C |
0.368 |
|
| 2013 |
Adabala PJ, LeGresley EB, Bance N, Niikura M, Pinto BM. Exploitation of the catalytic site and 150 cavity for design of influenza A neuraminidase inhibitors. The Journal of Organic Chemistry. 78: 10867-77. PMID 24090215 DOI: 10.1021/Jo401854W |
0.378 |
|
| 2013 |
Gu G, Adabala PJ, Szczepina MG, Borrelli S, Pinto BM. Synthesis and immunological characterization of modified hyaluronic acid hexasaccharide conjugates. The Journal of Organic Chemistry. 78: 8004-19. PMID 23848545 DOI: 10.1021/Jo4012442 |
0.35 |
|
| 2013 |
Greenway KT, LeGresley EB, Pinto BM. The influence of 150-cavity binders on the dynamics of influenza A neuraminidases as revealed by molecular dynamics simulations and combined clustering. Plos One. 8: e59873. PMID 23544106 DOI: 10.1371/Journal.Pone.0059873 |
0.313 |
|
| 2012 |
Jones K, Eskandari R, Naim HY, Pinto BM, Rose DR. Investigations of the structures and inhibitory properties of intestinal maltase glucoamylase and sucrase isomaltase. Journal of Pediatric Gastroenterology and Nutrition. 55: S20-4. PMID 23103645 DOI: 10.1097/01.Mpg.0000421403.34763.71 |
0.736 |
|
| 2012 |
Gilger M, Hamaker B, Nichols BL, Auricchio S, Treem WR, Naim HY, Heine M, Zimmer KP, Jones K, Eskandari R, Pinto BM, Rose DR, Lee BH, Quezada-Calvillo R, Adams B, et al. Research progress reported at the 50th Anniversary of the Discovery of Congenital Sucrase-Isomaltase Deficiency Workshop. Journal of Pediatric Gastroenterology and Nutrition. 55: S1. PMID 23103641 DOI: 10.1097/01.Mpg.0000422151.38401.69 |
0.714 |
|
| 2012 |
Greenway KT, Bischoff AG, Pinto BM. Probing hyperconjugation experimentally with the conformational deuterium isotope effect. The Journal of Organic Chemistry. 77: 9221-6. PMID 23025400 DOI: 10.1021/Jo3017988 |
0.309 |
|
| 2012 |
Lee BH, Eskandari R, Jones K, Reddy KR, Quezada-Calvillo R, Nichols BL, Rose DR, Hamaker BR, Pinto BM. Modulation of starch digestion for slow glucose release through "toggling" of activities of mucosal α-glucosidases. The Journal of Biological Chemistry. 287: 31929-38. PMID 22851177 DOI: 10.1074/Jbc.M112.351858 |
0.762 |
|
| 2012 |
Mohan S, McAtamney S, Jayakanthan K, Eskandari R, von Itzstein M, Pinto BM. Antiviral activities of sulfonium-ion glucosidase inhibitors and 5-thiomannosylamine disaccharide derivatives against dengue virus. International Journal of Antimicrobial Agents. 40: 273-6. PMID 22784856 DOI: 10.1016/J.Ijantimicag.2012.05.002 |
0.765 |
|
| 2012 |
Fernández-Herrera MA, López-Muñoz H, Hernández-Vázquez JM, Sánchez-Sánchez L, Escobar-Sánchez ML, Pinto BM, Sandoval-Ramírez J. Synthesis and selective anticancer activity of steroidal glycoconjugates. European Journal of Medicinal Chemistry. 54: 721-7. PMID 22770605 DOI: 10.1016/J.Ejmech.2012.06.027 |
0.345 |
|
| 2012 |
Zandberg WF, Gao N, Kumarasamy J, Lehrman MA, Seidah NG, Pinto BM. 5-thiomannosides block the biosynthesis of dolichol-linked oligosaccharides and mimic class I congenital disorders of glycosylation. Chembiochem : a European Journal of Chemical Biology. 13: 392-401. PMID 22262650 DOI: 10.1002/Cbic.201100647 |
0.341 |
|
| 2011 |
Eskandari R, Jones K, Reddy KR, Jayakanthan K, Chaudet M, Rose DR, Pinto BM. Probing the intestinal α-glucosidase enzyme specificities of starch-digesting maltase-glucoamylase and sucrase-isomaltase: synthesis and inhibitory properties of 3'- and 5'-maltose-extended de-O-sulfonated ponkoranol. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 14817-25. PMID 22127878 DOI: 10.1002/Chem.201102109 |
0.801 |
|
| 2011 |
Eskandari R, Jones K, Rose DR, Pinto BM. Selectivity of 3'-O-methylponkoranol for inhibition of N- and C-terminal maltase glucoamylase and sucrase isomaltase, potential therapeutics for digestive disorders or their sequelae. Bioorganic & Medicinal Chemistry Letters. 21: 6491-4. PMID 21924903 DOI: 10.1016/J.Bmcl.2011.08.069 |
0.776 |
|
| 2011 |
Eskandari R, Jones K, Rose DR, Pinto BM. The effect of heteroatom substitution of sulfur for selenium in glucosidase inhibitors on intestinal α-glucosidase activities. Chemical Communications (Cambridge, England). 47: 9134-6. PMID 21750824 DOI: 10.1039/C1Cc13052H |
0.788 |
|
| 2011 |
Fernández-Herrera MA, López-Muñoz H, Hernández-Vázquez JM, López-Dávila M, Mohan S, Escobar-Sánchez ML, Sánchez-Sánchez L, Pinto BM, Sandoval-Ramírez J. Synthesis and biological evaluation of the glycoside (25R)-3β,16β-diacetoxy-22-oxocholest-5-en-26-yl β-d-glucopyranoside: a selective anticancer agent in cervicouterine cell lines. European Journal of Medicinal Chemistry. 46: 3877-86. PMID 21703733 DOI: 10.1016/J.Ejmech.2011.05.058 |
0.329 |
|
| 2011 |
Jones K, Sim L, Mohan S, Kumarasamy J, Liu H, Avery S, Naim HY, Quezada-Calvillo R, Nichols BL, Pinto BM, Rose DR. Mapping the intestinal alpha-glucogenic enzyme specificities of starch digesting maltase-glucoamylase and sucrase-isomaltase. Bioorganic & Medicinal Chemistry. 19: 3929-34. PMID 21669536 DOI: 10.1016/J.Bmc.2011.05.033 |
0.379 |
|
| 2011 |
Zandberg WF, Benjannet S, Hamelin J, Pinto BM, Seidah NG. N-glycosylation controls trafficking, zymogen activation and substrate processing of proprotein convertases PC1/3 and subtilisin kexin isozyme-1. Glycobiology. 21: 1290-300. PMID 21527438 DOI: 10.1093/Glycob/Cwr060 |
0.345 |
|
| 2011 |
Albohy A, Mohan S, Zheng RB, Pinto BM, Cairo CW. Inhibitor selectivity of a new class of oseltamivir analogs against viral neuraminidase over human neuraminidase enzymes. Bioorganic & Medicinal Chemistry. 19: 2817-22. PMID 21489803 DOI: 10.1016/J.Bmc.2011.03.039 |
0.353 |
|
| 2010 |
Mohan S, Sim L, Rose DR, Pinto BM. Probing the active-site requirements of human intestinal N-terminal maltase-glucoamylase: Synthesis and enzyme inhibitory activities of a six-membered ring nitrogen analogue of kotalanol and its de-O-sulfonated derivative. Bioorganic & Medicinal Chemistry. 18: 7794-8. PMID 20970346 DOI: 10.1016/J.Bmc.2010.09.059 |
0.424 |
|
| 2010 |
Fernández-Herrera MA, Mohan S, López-Muñoz H, Hernández-Vázquez JM, Pérez-Cervantes E, Escobar-Sánchez ML, Sánchez-Sánchez L, Regla I, Pinto BM, Sandoval-Ramírez J. Synthesis of the steroidal glycoside (25R)-3β,16β-diacetoxy-12,22-dioxo-5α-cholestan-26-yl β-D-glucopyranoside and its anti-cancer properties on cervicouterine HeLa, CaSki, and ViBo cells. European Journal of Medicinal Chemistry. 45: 4827-37. PMID 20801554 DOI: 10.1016/J.Ejmech.2010.07.051 |
0.318 |
|
| 2010 |
Eskandari R, Jones K, Rose DR, Pinto BM. Probing the active-site requirements of human intestinal N-terminal maltase glucoamylase: the effect of replacing the sulfate moiety by a methyl ether in ponkoranol, a naturally occurring α-glucosidase inhibitor. Bioorganic & Medicinal Chemistry Letters. 20: 5686-9. PMID 20801033 DOI: 10.1016/J.Bmcl.2010.08.020 |
0.793 |
|
| 2010 |
Borrelli S, Zandberg WF, Mohan S, Ko M, Martinez-Gutierrez F, Partha SK, Sanders DA, Av-Gay Y, Pinto BM. Antimycobacterial activity of UDP-galactopyranose mutase inhibitors. International Journal of Antimicrobial Agents. 36: 364-8. PMID 20678902 DOI: 10.1016/J.Ijantimicag.2010.06.030 |
0.345 |
|
| 2010 |
Szczepina MG, Zheng RB, Completo GC, Lowary TL, Pinto BM. STD-NMR studies of two acceptor substrates of GlfT2, a galactofuranosyltransferase from Mycobacterium tuberculosis: epitope mapping studies. Bioorganic & Medicinal Chemistry. 18: 5123-8. PMID 20591680 DOI: 10.1016/J.Bmc.2010.05.069 |
0.33 |
|
| 2010 |
Zandberg WF, Mohan S, Kumarasamy J, Pinto BM. Capillary zone electrophoresis method for the separation of glucosidase inhibitors in extracts of Salacia reticulata, a plant used in ayurvedic treatments of type-2 diabetes. Analytical Chemistry. 82: 5323-30. PMID 20491445 DOI: 10.1021/Ac100843Y |
0.311 |
|
| 2010 |
Eskandari R, Jayakanthan K, Kuntz DA, Rose DR, Pinto BM. Synthesis of a biologically active isomer of kotalanol, a naturally occurring glucosidase inhibitor. Bioorganic & Medicinal Chemistry. 18: 2829-35. PMID 20363144 DOI: 10.1016/J.Bmc.2010.03.027 |
0.796 |
|
| 2010 |
Sim L, Willemsma C, Mohan S, Naim HY, Pinto BM, Rose DR. Structural basis for substrate selectivity in human maltase-glucoamylase and sucrase-isomaltase N-terminal domains. The Journal of Biological Chemistry. 285: 17763-70. PMID 20356844 DOI: 10.1074/Jbc.M109.078980 |
0.339 |
|
| 2010 |
Mohan S, Pinto BM. Towards the elusive structure of kotalanol, a naturally occurring glucosidase inhibitor. Natural Product Reports. 27: 481-8. PMID 20336233 DOI: 10.1039/B925950C |
0.358 |
|
| 2010 |
Eskandari R, Kuntz DA, Rose DR, Pinto BM. Potent glucosidase inhibitors: de-O-sulfonated ponkoranol and its stereoisomer. Organic Letters. 12: 1632-5. PMID 20218632 DOI: 10.1021/Ol1004005 |
0.784 |
|
| 2010 |
Mohan S, Jayakanthan K, Nasi R, Kuntz DA, Rose DR, Pinto BM. Synthesis and biological evaluation of heteroanalogues of kotalanol and de-O-sulfonated kotalanol. Organic Letters. 12: 1088-91. PMID 20143790 DOI: 10.1021/Ol100080M |
0.399 |
|
| 2010 |
Sim L, Jayakanthan K, Mohan S, Nasi R, Johnston BD, Pinto BM, Rose DR. New glucosidase inhibitors from an ayurvedic herbal treatment for type 2 diabetes: structures and inhibition of human intestinal maltase-glucoamylase with compounds from Salacia reticulata. Biochemistry. 49: 443-51. PMID 20039683 DOI: 10.1021/Bi9016457 |
0.4 |
|
| 2010 |
Randell KD, Johnston BD, Pinto BM. ChemInform Abstract: Novel 4-Thiogalactofuranosyl-Containing Disaccharides with Nitrogen in the Interglycosidic Linkage. Cheminform. 31: no-no. DOI: 10.1002/chin.200036220 |
0.771 |
|
| 2010 |
Randell KD, Johnston BD, Lee EE, Pinto BM. ChemInform Abstract: Synthesis of Oligosaccharide Fragments of the Glycosylinositolphospholipid of Trypanosoma cruzi: A New Selenoglycoside Glycosyl Donor for the Preparation of 4-Thiogalactofuranosyl Analogues. Cheminform. 31: no-no. DOI: 10.1002/chin.200024206 |
0.777 |
|
| 2009 |
Szczepina MG, Zheng RB, Completo GC, Lowary TL, Pinto BM. STD-NMR studies suggest that two acceptor substrates for GlfT2, a bifunctional galactofuranosyltransferase required for the biosynthesis of Mycobacterium tuberculosis arabinogalactan, compete for the same binding site. Chembiochem : a European Journal of Chemical Biology. 10: 2052-9. PMID 19575371 DOI: 10.1002/Cbic.200900202 |
0.324 |
|
| 2009 |
Hossany BR, Johnston BD, Wen X, Borrelli S, Yuan Y, Johnson MA, Pinto BM. Design, synthesis, and immunochemical characterization of a chimeric glycopeptide corresponding to the Shigella flexneri Y O-polysaccharide and its peptide mimic MDWNMHAA. Carbohydrate Research. 344: 1412-27. PMID 19467535 DOI: 10.1016/J.Carres.2009.03.029 |
0.343 |
|
| 2009 |
Jayakanthan K, Mohan S, Pinto BM. Structure proof and synthesis of kotalanol and de-O-sulfonated kotalanol, glycosidase inhibitors isolated from an herbal remedy for the treatment of type-2 diabetes. Journal of the American Chemical Society. 131: 5621-6. PMID 19331410 DOI: 10.1021/Ja900867Q |
0.445 |
|
| 2009 |
Mohan S, Pinto BM. Sulfonium-ion glycosidase inhibitors isolated from Salacia species used in traditional medicine, and related compounds Collection of Czechoslovak Chemical Communications. 74: 1117-1136. DOI: 10.1135/Cccc2009024 |
0.356 |
|
| 2008 |
Nasi R, Patrick BO, Sim L, Rose DR, Pinto BM. Studies directed toward the stereochemical structure determination of the naturally occurring glucosidase inhibitor, kotalanol: synthesis and inhibitory activities against human maltase glucoamylase of seven-carbon, chain-extended homologues of salacinol. The Journal of Organic Chemistry. 73: 6172-81. PMID 18651773 DOI: 10.1021/Jo800855N |
0.416 |
|
| 2008 |
Choubdar N, Bhat RG, Stubbs KA, Yuzwa S, Pinto BM. Synthesis of 2-amido, 2-amino, and 2-azido derivatives of the nitrogen analogue of the naturally occurring glycosidase inhibitor salacinol and their inhibitory activities against O-GlcNAcase and NagZ enzymes. Carbohydrate Research. 343: 1766-77. PMID 18358456 DOI: 10.1016/J.Carres.2008.02.027 |
0.755 |
|
| 2008 |
Jayakanthan K, Johnston BD, Pinto BM. Stereoselective synthesis of 4'-selenonucleosides using the Pummerer glycosylation reaction. Carbohydrate Research. 343: 1790-800. PMID 18316068 DOI: 10.1016/J.Carres.2008.02.014 |
0.36 |
|
| 2008 |
Choubdar N, Sim L, Rose DR, Pinto BM. Synthesis of 2-deoxy-2-fluoro and 1,2-ene derivatives of the naturally occurring glycosidase inhibitor, salacinol, and their inhibitory activities against recombinant human maltase glucoamylase. Carbohydrate Research. 343: 951-6. PMID 18295754 DOI: 10.1016/J.Carres.2008.01.025 |
0.415 |
|
| 2008 |
Kumar NS, Kuntz DA, Wen X, Pinto BM, Rose DR. Binding of sulfonium-ion analogues of di-epi-swainsonine and 8-epi-lentiginosine to Drosophila Golgi alpha-mannosidase II: the role of water in inhibitor binding. Proteins. 71: 1484-96. PMID 18076078 DOI: 10.1002/Prot.21850 |
0.358 |
|
| 2007 |
Chen W, Pinto BM. Synthesis of aza- and thia-spiroheterocycles and attempted synthesis of spiro sulfonium compounds related to salacinol. Carbohydrate Research. 342: 2163-72. PMID 17669386 DOI: 10.1016/J.Carres.2007.07.003 |
0.433 |
|
| 2007 |
Liu H, Nasi R, Jayakanthan K, Sim L, Heipel H, Rose DR, Pinto BM. New synthetic routes to chain-extended selenium, sulfur, and nitrogen analogues of the naturally occurring glucosidase inhibitor salacinol and their inhibitory activities against recombinant human maltase glucoamylase. The Journal of Organic Chemistry. 72: 6562-72. PMID 17658854 DOI: 10.1021/Jo071045M |
0.451 |
|
| 2007 |
Chen W, Sim L, Rose DR, Pinto BM. Synthesis of analogues of salacinol containing a carboxylate inner salt and their inhibitory activities against human maltase glucoamylase. Carbohydrate Research. 342: 1661-7. PMID 17597595 DOI: 10.1016/J.Carres.2007.06.003 |
0.479 |
|
| 2007 |
Bhat RG, Kumar NS, Pinto BM. Synthesis of phosphate derivatives related to the glycosidase inhibitor salacinol. Carbohydrate Research. 342: 1934-42. PMID 17572396 DOI: 10.1016/J.Carres.2007.05.030 |
0.748 |
|
| 2007 |
Mohan S, Pinto BM. Zwitterionic glycosidase inhibitors: salacinol and related analogues. Carbohydrate Research. 342: 1551-80. PMID 17559821 DOI: 10.1016/J.Carres.2007.05.014 |
0.35 |
|
| 2007 |
Nasi R, Sim L, Rose DR, Pinto BM. Synthesis and glycosidase inhibitory activities of chain-modified analogues of the glycosidase inhibitors salacinol and blintol. Carbohydrate Research. 342: 1888-94. PMID 17359953 DOI: 10.1016/J.Carres.2007.02.020 |
0.454 |
|
| 2007 |
Mohan S, Sim L, Rose DR, Pinto BM. Synthesis of S-alkylated sulfonium-ions and their glucosidase inhibitory activities against recombinant human maltase glucoamylase. Carbohydrate Research. 342: 901-12. PMID 17316580 DOI: 10.1016/J.Carres.2007.01.018 |
0.451 |
|
| 2007 |
Nasi R, Sim L, Rose DR, Pinto BM. New chain-extended analogues of salacinol and blintol and their glycosidase inhibitory activities. Mapping the active-site requirements of human maltase glucoamylase. The Journal of Organic Chemistry. 72: 180-6. PMID 17194097 DOI: 10.1021/Jo061944V |
0.447 |
|
| 2006 |
Gu G, Liu H, Pinto BM. Facile synthesis of sulfonium ion derivatives of 1,5-anhydro-5-thio-L-fucitol as potential alpha-L-fucosidase inhibitors. Carbohydrate Research. 341: 2478-86. PMID 16930571 DOI: 10.1016/J.Carres.2006.08.002 |
0.38 |
|
| 2006 |
Nasi R, Pinto BM. Synthesis of new analogues of salacinol containing a pendant hydroxymethyl group as potential glycosidase inhibitors. Carbohydrate Research. 341: 2305-11. PMID 16854397 DOI: 10.1016/J.Carres.2006.06.022 |
0.442 |
|
| 2006 |
Choubdar N, Pinto BM. Attempted synthesis of 2-acetamido and 2-amino derivatives of salacinol. Ring opening reactions. The Journal of Organic Chemistry. 71: 4671-4. PMID 16749804 DOI: 10.1021/Jo060167W |
0.347 |
|
| 2006 |
Kumar NS, Pinto BM. Synthesis of thioswainsonine as a potential glycosidase inhibitor. Carbohydrate Research. 341: 1685-91. PMID 16678808 DOI: 10.1016/J.Carres.2006.04.009 |
0.407 |
|
| 2006 |
Liu H, Sim L, Rose DR, Pinto BM. A new class of glucosidase inhibitor: analogues of the naturally occurring glucosidase inhibitor salacinol with different ring heteroatom substituents and acyclic chain extension. The Journal of Organic Chemistry. 71: 3007-13. PMID 16599595 DOI: 10.1021/Jo052539R |
0.442 |
|
| 2006 |
Kumar NS, Pinto BM. Synthesis and conformational analysis of bicyclic sulfonium salts. Structures related to the glycosidase inhibitor australine. The Journal of Organic Chemistry. 71: 2935-43. PMID 16599585 DOI: 10.1021/Jo051560P |
0.404 |
|
| 2006 |
Kumar NS, Pinto BM. Synthesis of a sulfonium ion analogue of the glycosidase inhibitor swainsonine. The Journal of Organic Chemistry. 71: 1262-4. PMID 16438551 DOI: 10.1021/Jo052111S |
0.342 |
|
| 2006 |
Johnston BD, Jensen HH, Pinto BM. Synthesis of sulfonium sulfate analogues of disaccharides and their conversion to chain-extended homologues of salacinol: new glycosidase inhibitors. The Journal of Organic Chemistry. 71: 1111-8. PMID 16438529 DOI: 10.1021/Jo052252U |
0.437 |
|
| 2006 |
Watts JK, Sadalapure K, Choubdar N, Pinto BM, Damha MJ. Synthesis and conformational analysis of 2'-fluoro-5-methyl-4'-thioarabinouridine (4'S-FMAU). The Journal of Organic Chemistry. 71: 921-5. PMID 16438502 DOI: 10.1021/Jo051844+ |
0.378 |
|
| 2006 |
Liu H, Pinto BM. Design and synthesis of selenonium and sulfonium ions related to the naturally occurring glucosidase inhibitor salacinol Canadian Journal of Chemistry. 84: 1351-1362. DOI: 10.1139/V06-100 |
0.434 |
|
| 2006 |
Liu H, Pinto BM. Synthesis of zwitterionic selenonium and sulfonium sulfates from D-mannose as potential glycosidase inhibitors Canadian Journal of Chemistry. 84: 497-505. DOI: 10.1139/V06-027 |
0.426 |
|
| 2005 |
Kumar NS, Pinto BM. Synthesis of D-lyxitol and D-ribitol analogues of the naturally occurring glycosidase inhibitor salacinol. Carbohydrate Research. 340: 2612-9. PMID 16198322 DOI: 10.1016/J.Carres.2005.09.004 |
0.425 |
|
| 2005 |
Michon F, Moore SL, Kim J, Blake MS, Auzanneau FI, Johnston BD, Johnson MA, Pinto BM. Doubly branched hexasaccharide epitope on the cell wall polysaccharide of group A streptococci recognized by human and rabbit antisera. Infection and Immunity. 73: 6383-9. PMID 16177309 DOI: 10.1128/Iai.73.10.6383-6389.2005 |
0.312 |
|
| 2005 |
Liu H, Pinto BM. Efficient synthesis of the glucosidase inhibitor blintol, the selenium analogue of the naturally occurring glycosidase inhibitor salacinol. The Journal of Organic Chemistry. 70: 753-5. PMID 15651838 DOI: 10.1021/Jo048058+ |
0.412 |
|
| 2005 |
Chakka N, Johnston BD, Pinto BM. Synthesis and conformational analysis of disaccharide analogues containing disulfide and selenosulfide functionalities in the interglycosidic linkages Canadian Journal of Chemistry. 83: 929-936. DOI: 10.1139/V05-107 |
0.392 |
|
| 2005 |
Kavlekar LM, Kuntz DA, Wen X, Johnston BD, Svensson B, Rose DR, Pinto BM. 5-Thio-d-glycopyranosylamines and their amidinium salts as potential transition-state mimics of glycosyl hydrolases: synthesis, enzyme inhibitory activities, X-ray crystallography, and molecular modeling Tetrahedron: Asymmetry. 16: 1035-1046. DOI: 10.1016/J.Tetasy.2005.01.021 |
0.432 |
|
| 2005 |
Kuntz DA, Ghavami A, Johnston BD, Pinto BM, Rose DR. Crystallographic analysis of the interactions of Drosophila melanogaster Golgi α-mannosidase II with the naturally occurring glycomimetic salacinol and its analogues Tetrahedron: Asymmetry. 16: 25-32. DOI: 10.1016/J.Tetasy.2004.11.057 |
0.372 |
|
| 2004 |
Szczepina MG, Johnston BD, Yuan Y, Svensson B, Pinto BM. Synthesis of alkylated deoxynojirimycin and 1,5-dideoxy-1,5-iminoxylitol analogues: polar side-chain modification, sulfonium and selenonium heteroatom variants, conformational analysis, and evaluation as glycosidase inhibitors. Journal of the American Chemical Society. 126: 12458-69. PMID 15453780 DOI: 10.1021/Ja0482076 |
0.448 |
|
| 2004 |
Veerapen N, Yuan Y, Sanders DA, Pinto BM. Synthesis of novel ammonium and selenonium ions and their evaluation as inhibitors of UDP-galactopyranose mutase. Carbohydrate Research. 339: 2205-17. PMID 15337448 DOI: 10.1016/J.Carres.2004.07.012 |
0.471 |
|
| 2003 |
Johnson MA, Jensen MT, Svensson B, Pinto BM. Selection of a high-energy bioactive conformation of a sulfonium-ion glycosidase inhibitor by the enzyme glucoamylase G2. Journal of the American Chemical Society. 125: 5663-70. PMID 12733904 DOI: 10.1021/Ja0212617 |
0.346 |
|
| 2003 |
Ghavami A, Sadalapure KS, Johnston BD, Lobera M, Snider BB, Pinto BM. Improved syntheses of the naturally occurring glycosidase inhibitor salacinol Synlett. 1259-1262. DOI: 10.1055/S-2003-40353 |
0.385 |
|
| 2002 |
Johnson MA, Pinto BM. Saturation transfer difference 1D-TOCSY experiments to map the topography of oligosaccharides recognized by a monoclonal antibody directed against the cell-wall polysaccharide of group A streptococcus. Journal of the American Chemical Society. 124: 15368-74. PMID 12487612 DOI: 10.1021/Ja020983V |
0.33 |
|
| 2002 |
Höög C, Rotondo A, Johnston BD, Pinto BM. Synthesis and conformational analysis of a pentasaccharide corresponding to the cell-wall polysaccharide of the Group A Streptococcus. Carbohydrate Research. 337: 2023-36. PMID 12433468 DOI: 10.1016/S0008-6215(02)00218-5 |
0.337 |
|
| 2002 |
Vyas NK, Vyas MN, Chervenak MC, Johnson MA, Pinto BM, Bundle DR, Quiocho FA. Molecular recognition of oligosaccharide epitopes by a monoclonal Fab specific for Shigella flexneri Y lipopolysaccharide: X-ray structures and thermodynamics. Biochemistry. 41: 13575-86. PMID 12427018 DOI: 10.1021/Bi0261387 |
0.332 |
|
| 2002 |
Johnston BD, Ghavami A, Jensen MT, Svensson B, Pinto BM. Synthesis of selenium analogues of the naturally occurring glycosidase inhibitor salacinol and their evaluation as glycosidase inhibitors. Journal of the American Chemical Society. 124: 8245-50. PMID 12105902 DOI: 10.1021/Ja020299G |
0.448 |
|
| 2002 |
Johnson MA, Rotondo A, Pinto BM. NMR studies of the antibody-bound conformation of a carbohydrate-mimetic peptide. Biochemistry. 41: 2149-57. PMID 11841205 DOI: 10.1021/Bi011927U |
0.308 |
|
| 2002 |
Ghavami A, Johnston BD, Maddess MD, Chinapoo SM, Jensen MT, Svensson B, Pinto BM. Synthesis of 1,4-anhydro-D-xylitol heteroanalogues of the naturally occurring glycosidase inhibitor salacinol and their evaluation as glycosidase inhibitors Canadian Journal of Chemistry. 80: 937-942. DOI: 10.1139/V02-078 |
0.431 |
|
| 2002 |
Diaz-Quijada GA, Weinberg N, Holdcroft S, Pinto BM. Investigation of barriers to conformational interchange in oligothiophenes and oligo(thienyl)furans Journal of Physical Chemistry A. 106: 1266-1276. DOI: 10.1021/Jp011783T |
0.733 |
|
| 2001 |
Ghavami A, Johnston BD, Jensen MT, Svensson B, Pinto BM. Synthesis of nitrogen analogues of salacinol and their evaluation as glycosidase inhibitors. Journal of the American Chemical Society. 123: 6268-71. PMID 11427050 DOI: 10.1021/ja0103750 |
0.332 |
|
| 2001 |
Ghavami A, Johnston BD, Pinto BM. A new class of glycosidase inhibitor: synthesis of salacinol and its stereoisomers. The Journal of Organic Chemistry. 66: 2312-7. PMID 11281771 DOI: 10.1021/Jo001444G |
0.397 |
|
| 2001 |
Batchelor RJ, Green DF, Johnston BD, Patrick BO, Pinto BM. Conformational preferences in glycosylamines. implications for the exo-anomeric effect. Carbohydrate Research. 330: 421-6. PMID 11270822 DOI: 10.1016/S0008-6215(00)00304-9 |
0.343 |
|
| 2000 |
Weimar T, Petersen BO, Svensson B, Pinto BM. Determination of the solution conformation of D-gluco-dihydroacarbose, a high-affinity inhibitor bound to glucoamylase by transferred NOE NMR spectroscopy. Carbohydrate Research. 326: 50-5. PMID 16001506 DOI: 10.1016/S0008-6215(00)00021-5 |
0.316 |
|
| 2000 |
Johnston BD, Pinto BM. Synthesis of thio-linked disaccharides by 1-->2 intramolecular thioglycosyl migration: oxacarbenium versus episulfonium ion intermediates. The Journal of Organic Chemistry. 65: 4607-17. PMID 10959866 DOI: 10.1021/Jo000226K |
0.363 |
|
| 2000 |
Randell KD, Johnston BD, Pinto BM. Novel 4-thiogalactofuranosyl-containing disaccharides with nitrogen in the interglycosidic linkage. Carbohydrate Research. 326: 145-50. PMID 10877097 DOI: 10.1016/S0008-6215(00)00044-6 |
0.776 |
|
| 2000 |
Randell KD, Johnston BD, Brown PN, Pinto BM. Synthesis of galactofuranosyl-containing oligosaccharides corresponding to the glycosylinositolphospholipid of Trypanosoma cruzi. Carbohydrate Research. 325: 253-64. PMID 10839119 DOI: 10.1016/S0008-6215(00)00007-0 |
0.785 |
|
| 2000 |
Randell KD, Johnston BD, Green DF, Pinto BM. Is there a generalized reverse anomeric Effect? substituent and solvent effects on the configurational equilibria of neutral and protonated N-arylglucopyranosylamines and N-aryl-5-thioglucopyranosylamines The Journal of Organic Chemistry. 65: 220-6. PMID 10813919 DOI: 10.1021/Jo991520J |
0.766 |
|
| 2000 |
Weimar T, Stoffer B, Svensson B, Pinto BM. Complexes of glucoamylase with maltoside heteroanalogues: bound ligand conformations by use of transferred NOE experiments and molecular modeling. Biochemistry. 39: 300-6. PMID 10630989 DOI: 10.1021/Bi991645I |
0.337 |
|
| 2000 |
Mcleod RG, Johnston BD, Pinto BM. A generalizedexo-anomeric effect. Substituent and solvent effects on the conformational equilibria of 2-(arylseleno)cyclohexanones Israel Journal of Chemistry. 40: 307-316. DOI: 10.1560/Gyn6-1Prq-6Kgf-0Lva |
0.345 |
|
| 2000 |
Svansson L, Johnston BD, Gu J, Patrick B, Pinto BM. Synthesis and Conformational Analysis of a Sulfonium-Ion Analogue of the Glycosidase Inhibitor Castanospermine Journal of the American Chemical Society. 122: 10769-10775. DOI: 10.1021/Ja002038H |
0.374 |
|
| 2000 |
Randell KD, Johnston BD, Lee EE, Pinto B. Synthesis of oligosaccharide fragments of the glycosylinositolphospholipid of Trypanosoma cruzi: a new selenoglycoside glycosyl donor for the preparation of 4-thiogalactofuranosyl analogues Tetrahedron: Asymmetry. 11: 207-222. DOI: 10.1016/S0957-4166(99)00498-X |
0.802 |
|
| 1999 |
Randell KD, Frandsen TP, Stoffer B, Johnson MA, Svensson B, Pinto BM. Synthesis and glycosidase inhibitory activity of 5-thioglucopyranosylamines. Molecular modeling of complexes with glucoamylase. Carbohydrate Research. 321: 143-56. PMID 10614065 DOI: 10.1016/S0008-6215(99)00177-9 |
0.791 |
|
| 1999 |
Johnston BD, Pinto BM. Use of a phenyl 1-selenogalactofuranoside as a glycosyl donor for the synthesis of galactofuranosyl-containing disaccharides. Carbohydrate Research. 315: 356-60. PMID 10399306 DOI: 10.1016/S0008-6215(99)00024-5 |
0.395 |
|
| 1999 |
Woranovicz SM, Pinto BM, Gorin PA, Iacomini M. Novel structures in galactoglucomannans of the lichens Cladonia substellata and Cladonia ibitipocae: significance as chemotypes. Phytochemistry. 51: 395-402. PMID 10382316 DOI: 10.1016/S0031-9422(99)00005-9 |
0.346 |
|
| 1998 |
Wu X, Mariño-Albernas JR, Auzanneau FI, Verez-Bencomo V, Pinto BM. Synthesis and NMR analysis of 13C-labeled oligosaccharides corresponding to the major glycolipid from Mycobacterium leprae. Carbohydrate Research. 306: 493-503. PMID 9679274 DOI: 10.1016/S0008-6215(97)10101-X |
0.38 |
|
| 1998 |
Johnston BD, Pinto B. Synthesis of heteroanalogues of disaccharides as potential inhibitors of the processing mannosidase Class I enzymes Carbohydrate Research. 310: 17-25. DOI: 10.1016/S0008-6215(98)00162-1 |
0.41 |
|
| 1997 |
Johnston BD, Pinto BM. Use of a phenyl 1-selenogalactofuranoside as a glycosyl donor for the synthesis of galactofuranosyl-containing disaccharides. Carbohydrate Research. 305: 289-92. PMID 9581281 DOI: 10.1016/S0008-6215(97)10016-7 |
0.395 |
|
| 1997 |
Kreis UC, Varma V, Pinto BM. Oligosaccharides corresponding to biological repeating units of Shigella flexneri variant Y polysaccharide Part 5. Conformational analysis of a heptasaccharide hapten utilizing a combined molecular dynamics and NMR spectroscopic protocol Journal of Molecular Structure-Theochem. 389-409. DOI: 10.1016/S0166-1280(96)04541-1 |
0.318 |
|
| 1996 |
Auzanneau FI, Pinto BM. Preparations of antigens and immunoadsorbents corresponding to the Streptococcus group A cell-wall polysaccharide. Bioorganic & Medicinal Chemistry. 4: 2003-10. PMID 9007283 DOI: 10.1016/S0968-0896(96)00183-6 |
0.3 |
|
| 1996 |
Auzanneau FI, Forooghian F, Pinto BM. Efficient, convergent syntheses of oligosaccharide allyl glycosides corresponding to the Streptococcus group A cell-wall polysaccharide. Carbohydrate Research. 291: 21-41. PMID 8864221 DOI: 10.1016/S0008-6215(96)00152-8 |
0.355 |
|
| 1995 |
Stuike-Prill R, Pinto BM. Conformational analysis of oligosaccharides corresponding to the cell-wall polysaccharide of the Streptococcus group A by Metropolis Monte Carlo simulations. Carbohydrate Research. 279: 59-73. PMID 8593633 DOI: 10.1016/0008-6215(95)00279-0 |
0.348 |
|
| 1995 |
Andrews JS, Pinto BM. Synthesis of a thio analogue of n-propyl kojibioside, a potential glucosidase inhibitor. Carbohydrate Research. 270: 51-62. PMID 7627988 DOI: 10.1016/0008-6215(95)00014-K |
0.379 |
|
| 1995 |
Kreis UC, Varma V, Pinto BM. Application of two-dimensional NMR spectroscopy and molecular dynamics simulations to the conformational analysis of oligosaccharides corresponding to the cell-wall polysaccharide of Streptococcus group A. International Journal of Biological Macromolecules. 17: 117-30. PMID 7577810 DOI: 10.1016/0141-8130(95)92678-J |
0.33 |
|
| 1995 |
Mehta S, Andrews JS, Svensson B, Pinto BM. Synthesis and Enzymic Activity of Novel Glycosidase Inhibitors Containing Sulfur and Selenium Journal of the American Chemical Society. 117: 9783-9790. DOI: 10.1021/Ja00144A001 |
0.367 |
|
| 1994 |
Mehta S, Andrews JS, Johnston BD, Pinto BM. Novel Hetero-analogs of Methyl Maltoside Containing Sulfur and Selenium as Potential Glycosidase Inhibitors Journal of the American Chemical Society. 116: 1569-1570. DOI: 10.1021/Ja00083A052 |
0.344 |
|
| 1994 |
Mehta S, Jordan KL, Weimar T, Kreis UC, Batchelor RJ, Einstein FW, Pinto B. Synthesis of sulfur analogues of methyl and allyl kojibiosides and methyl isomaltoside and conformational analysis of the kojibiosides Tetrahedron: Asymmetry. 5: 2367-2396. DOI: 10.1016/S0957-4166(00)80386-9 |
0.389 |
|
| 1993 |
Marino-Albernas JR, Harris SL, Varma V, Pinto BM. Convergent synthesis of an elusive hexasaccharide corresponding to the cell-wall polysaccharide of the β-hemolytic Streptococcus Group A Carbohydrate Research. 245: 245-257. PMID 8370024 DOI: 10.1016/0008-6215(93)80075-P |
0.367 |
|
| 1993 |
Mehta S, Pinto BM. Novel glycosidation methodology. The use of phenyl selenoglycosides as glycosyl donors and acceptors in oligosaccharide synthesis Journal of Organic Chemistry. 58: 3269-3276. DOI: 10.1021/Jo00064A012 |
0.365 |
|
| 1992 |
Mehta S, Pinto BM. Unprecedented chemical glycosidation of 5-thioglucose to give disaccharides.☆ Tetrahedron Letters. 33: 7675-7678. DOI: 10.1016/0040-4039(93)88013-9 |
0.364 |
|
| 1991 |
Mehta S, Pinto BM. Phenylselenoglycosides as novel, versatile glycosyl donors. Selective activation over thioglycosides Tetrahedron Letters. 32: 4435-4438. DOI: 10.1016/0040-4039(91)80005-Q |
0.315 |
|
| 1990 |
Pinto BM, Reimer KB, Morissette DG, Bundle DR. Synthesis and 2D-n.m.r. analysis of a pentasaccharide glycoside of the biological repeating units of Shigella flexneri variant Y polysaccharide and the preparation of a synthetic antigen Carbohydrate Research. 196: 156-166. PMID 2189552 DOI: 10.1016/0008-6215(90)84115-B |
0.348 |
|
| 1990 |
Andrews JS, Pinto BM. Oligosaccharides corresponding to the antigenic determinants of the β-haemolytic Streptococci Group A. Part 2. Synthesis and 2D nuclear magnetic resonance analysis of a branched tetrasaccharide hapten Journal of the Chemical Society-Perkin Transactions 1. 1785-1792. DOI: 10.1039/P19900001785 |
0.384 |
|
| 1990 |
Pinto BM, Reimer KB, Morissette DG, Bundle DR. Oligosaccharides corresponding to biological repeating units of Shigella flexneri variant Y polysaccharide: Part 3. Synthesis and 2D-Nuclear magnetic resonance analysis of a heptasaccharide hapten Journal of the Chemical Society, Perkin Transactions 1. 293-299. DOI: 10.1039/P19900000293 |
0.306 |
|
| 1990 |
Pinto BM, Buiting MMW, Reimer KB. Use of the [.beta.-(trimethylsilyl)ethoxy]methyl (SEM) protecting group in carbohydrate chemistry. Fully functionalized rhamnose acceptors and donors for use in oligosaccharide synthesis Journal of Organic Chemistry. 55: 2177-2181. DOI: 10.1021/Jo00294A036 |
0.366 |
|
| 1989 |
Pinto BM, Johnston BD, Nagelkerke R, Juaristi E, González EA. A dynamic NMR study of the nitrogen lone pair orientation in 2-benzoyl-5-methyl-5-aza-1,3-dithiacyclohexane Canadian Journal of Chemistry. 67: 2067-2070. DOI: 10.1139/V89-321 |
0.336 |
|
| 1989 |
Pinto BM, Reimer KB, Morissette DG, Bundle DR. Oligosaccharides corresponding to biological repeating units of Shigella flexneri variant Y polysaccharide. 2. Synthesis and two-dimensional NMR analysis of a hexasaccharide hapten Journal of Organic Chemistry. 54: 2650-2656. DOI: 10.1021/Jo00272A038 |
0.319 |
|
| 1988 |
Reimer KB, Pinto BM. Synthesis of oligosaccharides corresponding to the antigenic determinants of the β-haemolytic Streptococci Group A. Part 1. Overall strategy and synthesis of a linear trisaccharide Journal of the Chemical Society-Perkin Transactions 1. 2103-2111. DOI: 10.1039/P19880002103 |
0.398 |
|
| 1987 |
Pinto BM, Morissette DG, Bundle DR. Synthesis of oligosaccharides corresponding to biological repeating units of Shigella flexneri variant Y polysaccharide. Part 1. Overall strategy, synthesis of a key trisaccharide intermediate, and synthesis of a pentasaccharide Journal of the Chemical Society, Perkin Transactions 1. 9-14. DOI: 10.1039/P19870000009 |
0.378 |
|
| 1986 |
Pinto BM, Sandoval-Ramírez J, Sharma RD. A Convenient Synthesis of 4,4′-Dimethylaminodiphenyl Diselenide and 4,4′-Dinitrodiphenyl Diselenide Synthetic Communications. 16: 553-557. DOI: 10.1080/00397918608078772 |
0.325 |
|
| 1986 |
Pinto BM, Grindley TB, Szarek WA. Effects of substitution on nitrogen on barriers to rotation of amides. III—effect of the variation of ring size of cyclic substituents Magnetic Resonance in Chemistry. 24: 323-331. DOI: 10.1002/Mrc.1260240411 |
0.541 |
|
| 1985 |
Szarek WA, Pinto BM, Iwakawa M. Nucleoside analogs involving modifications in the carbohydrate ring: nuclear magnetic resonance spectroscopic studies Canadian Journal of Chemistry. 63: 2162-2168. DOI: 10.1139/V85-355 |
0.526 |
|
| 1985 |
Szarek WA, Pinto BM, Iwakawa M. Synthesis and biological activity of nucleoside analogs involving modifications in the carbohydrate ring Canadian Journal of Chemistry. 63: 2149-2161. DOI: 10.1139/V85-354 |
0.573 |
|
| 1984 |
Pinto BM, Szarek WA, Grindley TB. Effects of substitution on nitrogen on barriers to rotation of amides. 2—Evaluation of the importance of resonance effects Organic Magnetic Resonance. 22: 676-692. DOI: 10.1002/Mrc.1270221103 |
0.503 |
|
| 1983 |
SZAREK WA, PINTO BM, GRINDLEY TB. ChemInform Abstract: A HIGHLY STEREOSELECTIVE INTRAMOLECULAR ALDOL CONDENSATION. PART II. SYNTHESIS OF DL-HAMAMELOSE FROM 2,2′-O-METHYLENEBIS(D-GLYCEROSE) Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198332331 |
0.505 |
|
| 1983 |
Szarek WA, Pinto BM, Grindley TB. A highly stereoselective intramolecular aldol condensation. Part II. Synthesis of D,L-hamamelose from 2,2′-O-methylene-bis-D-glycerose Canadian Journal of Chemistry. 61: 461-469. DOI: 10.1002/Chin.198332331 |
0.536 |
|
| 1982 |
SZAREK WA, PINTO BM, HAINES AH, GRINDLEY TB. ChemInform Abstract: A HIGHLY STEREOSELECTIVE INTRAMOLECULAR ALDOL CONDENSATION. PART I. NUCLEAR MAGNETIC RESONANCE SPECTROSCOPIC INVESTIGATION OF THE STEREOCHEMISTRY OF THE PRODUCTS DERIVED FROM THE REACTION OF 2,2′-O-METHYLENE-BIS-D-GLYCEROSE WITH BASE Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198226304 |
0.487 |
|
| 1982 |
Szarek WA, Pinto BM, Haines AH, Grindley TB. A highly stereoselective intramolecular aldol condensation. Part I. Nuclear magnetic resonance spectroscopic investigation of the stereochemistry of the products derived from the reaction of 2,2′-O-methylene-bis-D-glycerose with base Canadian Journal of Chemistry. 60: 390-414. DOI: 10.1002/Chin.198226304 |
0.536 |
|
| 1981 |
Cameron TS, Cordes RE, Pinto BM, Szarek WA. Crystal and molecular structure of cis,anti,cis-N,N′-dibenzoyl-3,12-diazatricyclo[6.4.0.02,7]dodecan-6,12-dione and cis,anti,cis-N,N′-dibenzoyl-3,9-diazatricyclo[6.4.0.02,7]dodecan-6,9-dione. Photodimers of N-benzoylcyclohex-2-ene-4-one Canadian Journal of Chemistry. 59: 3136-3140. DOI: 10.1139/V81-457 |
0.473 |
|
| 1978 |
Iwakawa M, Pinto BM, Szarek WA. Synthetic routes to nucleoside analogs of N-substituted 1,3-thiazolidines Canadian Journal of Chemistry. 56: 326-335. DOI: 10.1002/Chin.197824256 |
0.519 |
|
| 1978 |
IWAKAWA M, PINTO BM, SZAREK WA. ChemInform Abstract: SYNTHETIC ROUTES TO NUCLEOSIDE ANALOGS OF N-SUBSTITUTED 1,3-THIAZOLIDINES Chemischer Informationsdienst. 9. DOI: 10.1002/chin.197824256 |
0.48 |
|
| 1977 |
Pinto BM, Vyas DM, Szarek WA. Synthetic routes to nucieoside analogs of N-substituted 1-oxa-4-azacyclohexanes and 1-thia-4-azacyclohexanes. 13C nuclear magnetic resonance spectra of six-membered, cyclic amides Canadian Journal of Chemistry. 55: 937-948. DOI: 10.1139/V77-132 |
0.57 |
|
| 1977 |
PINTO BM, VYAS DM, SZAREK WA. ChemInform Abstract: SYNTHETIC ROUTES TO NUCLEOSIDE ANALOGS OF N-SUBSTITUTED 1-OXA-4-AZACYCLOHEXANES AND 1-THIA-4-AZACYCLOHEXANES. CARBON-13 NUCLEAR MAGNETIC RESONANCE SPECTRA OF SIX-MEMBERED, CYCLIC AMIDES Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/Chin.197727239 |
0.442 |
|
| 1977 |
GRINDLEY TB, PINTO BM, SZAREK WA. ChemInform Abstract: EFFECTS OF SUBSTITUTION ON NITROGEN ON BARRIERS TO ROTATION OF CYCLIC AMIDES. PART I. INVESTIGATION OF THE ROTATIONAL BARRIER IN 4-BENZOYL-1-THIA-4-AZACYCLOHEX-2-ENE BY PROTON DYNAMIC NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY Chemischer Informationsdienst. 8: no-no. DOI: 10.1002/chin.197727079 |
0.412 |
|
| 1977 |
Grindley TB, Pinto BM, Szarek WA. Effects of substitution on nitrogen on barriers to rotation of cyclic amides. Part I. Investigation of the rotational barier in 4-benzoyl-1-thia-4-azacyclohex-2-ene by 1H dynamic nuclear magnetic resonance spectroscopy Canadian Journal of Chemistry. 55: 949-957. DOI: 10.1002/Chin.197727079 |
0.523 |
|
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