| Year |
Citation |
Score |
| 2013 |
Della Felice F, Rúveda EA, Stortz CA, Colombo MI. Differential O-3/O-4 selectivity in the glycosylation of N-dimethylmaleoyl-protected hexosamine acceptors: effect of a conformationally armed (superarmed) glycosyl donor. Carbohydrate Research. 380: 167-73. PMID 24036392 DOI: 10.1016/J.Carres.2013.08.002 |
0.451 |
|
| 2012 |
Colombo MI, Rúveda EA, Gorlova O, Lalancette R, Stortz CA. Structural analysis of methyl 6-O-benzyl-2-deoxy-2-dimethylmaleimido-α-D-allopyranoside by X-ray crystallography, NMR, and QM calculations: hydrogen bonding and comparison of density functionals. Carbohydrate Research. 353: 79-85. PMID 22520505 DOI: 10.1016/J.Carres.2012.03.025 |
0.401 |
|
| 2011 |
Colombo MI, Rúveda EA, Stortz CA. Regioselectivity of the glycosylation of N-dimethylmaleoyl-protected hexosamine acceptors. An experimental and DFT approach. Organic & Biomolecular Chemistry. 9: 3020-5. PMID 21380458 DOI: 10.1039/C1Ob00021G |
0.753 |
|
| 2011 |
Colombo MI, Stortz CA, Rúveda EA. A comparative study of the O-3 reactivity of isomeric N-dimethylmaleoyl-protected D-glucosamine and D-allosamine acceptors. Carbohydrate Research. 346: 569-76. PMID 21320701 DOI: 10.1016/J.Carres.2011.01.017 |
0.749 |
|
| 2010 |
Colombo MI, Zinczuk J, Mischne MP, Ruveda EA. ChemInform Abstract: A Concise Synthesis of (+)-Cassiol. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200141251 |
0.681 |
|
| 2010 |
BACIGALUPPO JA, COLOMBO MI, ZINCZUK J, HUBER SN, MISCHNE MP, RUVEDA EA. ChemInform Abstract: Convenient and Short Route to a Key Intermediate (VI) in the Synthesis of Forskolin. Cheminform. 23: no-no. DOI: 10.1002/chin.199208185 |
0.683 |
|
| 2010 |
ZINCZUK J, BACIGALUPPO JA, MISCHNE MP, COLOMBO MI, RUVEDA EA. ChemInform Abstract: An Improved Preparation of a Tricyclic Lactone, a Potentially Useful Precursor of Highly Functionalized Terpenoids. Cheminform. 23: no-no. DOI: 10.1002/chin.199201157 |
0.653 |
|
| 2008 |
Bohn ML, Colombo MI, Rúveda EA, Stortz CA. Conformational and electronic effects on the regioselectivity of the glycosylation of different anomers of N-dimethylmaleoyl-protected glucosamine acceptors. Organic & Biomolecular Chemistry. 6: 554-61. PMID 18219427 DOI: 10.1039/B715847E |
0.757 |
|
| 2007 |
Bohn ML, Colombo MI, Pisano PL, Stortz CA, Rúveda EA. Differential O-3/O-4 regioselectivity in the glycosylation of alpha and beta anomers of 6-O-substituted N-dimethylmaleoyl-protected D-glucosamine acceptors. Carbohydrate Research. 342: 2522-36. PMID 17880931 DOI: 10.1016/J.Carres.2007.08.006 |
0.749 |
|
| 2007 |
Justribó V, Pellegrinet SC, Colombo MI. Studies on the intramolecular cyclizations of bicyclic delta-hydroxynitriles promoted by triflic anhydride. The Journal of Organic Chemistry. 72: 3702-12. PMID 17439177 DOI: 10.1021/Jo062669F |
0.388 |
|
| 2006 |
Bohn ML, Colombo MI, Stortz CA, Rúveda EA. A comparative study of the influence of some protecting groups on the reactivity of D-glucosamine acceptors with a galactofuranosyl donor. Carbohydrate Research. 341: 1096-104. PMID 16630599 DOI: 10.1016/J.Carres.2006.03.030 |
0.753 |
|
| 2004 |
Justribo V, Colombo MI. An Unexpected Result in an Intramolecular Ritter Reaction Induced by Triflic Anhydride. Cheminform. 35. DOI: 10.1016/J.Tetlet.2003.08.107 |
0.312 |
|
| 2003 |
Zinczuk J, Bacigaluppo JA, Colombo MI, Cravero RM, González-Sierra M, Rúveda EA. An efficient and environmentally benign chemical synthesis of testolactone Journal of the Brazilian Chemical Society. 14. DOI: 10.1590/S0103-50532003000600013 |
0.676 |
|
| 2003 |
Colombo MI, Zinczuk J, Bohn ML, Rúveda EA. Detours en route to a total synthesis of (+)-cassiol Tetrahedron: Asymmetry. 14: 717-725. DOI: 10.1016/S0957-4166(03)00082-X |
0.391 |
|
| 2002 |
Colombo MI, Bohn ML, Rúveda EA. The Mechanism of the Ritter Reaction in Combination with Wagner-Meerwein Rearrangements. A Cooperative Learning Experience Journal of Chemical Education. 79: 484. DOI: 10.1021/Ed079P484 |
0.309 |
|
| 2002 |
Pellegrinet SC, Colombo MI, Testero SA, Sierra MG, R�veda EA. A New Laboratory Experiment Based on a Chemical Transformation of Santonin: Synthesis of Santonic Acid The Chemical Educator. 7: 155-158. DOI: 10.1007/S00897020561A |
0.746 |
|
| 2001 |
Colombo MI, Zinczuk J, Mischne MP, Rúveda EA. Studies directed toward the preparation of key intermediates for the synthesis of trisporic acids and cassiol Pure and Applied Chemistry. 73: 623-626. DOI: 10.1351/Pac200173030623 |
0.721 |
|
| 2001 |
Colombo MI, Zinczuk J, Mischne MP, Rúveda EA. A concise synthesis of (+)-cassiol Tetrahedron: Asymmetry. 12: 1251-1253. DOI: 10.1016/S0957-4166(01)00222-1 |
0.695 |
|
| 2000 |
Colombo M, Bacigaluppo J, Zinczuk J, Mischne M, Rúveda E. Studies on a New Synthetic Route towards Cassiol Molecules. 5: 505-507. DOI: 10.3390/50300505 |
0.705 |
|
| 2000 |
Colombo M, Bacigaluppo J, Mischne M, Zinczuk J, Rúveda E. Applications of Olefination Reactions to Cassiol Synthesis Molecules. 5: 327-329. DOI: 10.3390/50300327 |
0.696 |
|
| 1998 |
Marder M, Viola H, Bacigaluppo JA, Colombo MI, Wasowski C, Wolfman C, Medina JH, Rúveda EA, Paladini AC. Detection of benzodiazepine receptor ligands in small libraries of flavone derivatives synthesized by solution phase combinatorial chemistry. Biochemical and Biophysical Research Communications. 249: 481-5. PMID 9712722 DOI: 10.1006/Bbrc.1998.9146 |
0.687 |
|
| 1997 |
Marder M, Zinczuk J, Colombo MI, Wasowski C, Viola H, Wolfman C, Medina JH, Rúveda EA, Paladini AC. Synthesis of halogenated/nitrated flavone derivatives and evaluation of their affinity for the central benzodiazepine receptor Bioorganic and Medicinal Chemistry Letters. 7: 2003-2008. DOI: 10.1016/S0960-894X(97)00343-0 |
0.329 |
|
| 1996 |
Bacigaluppo JA, Colombo MI, Preite MD, Zinczuk J, Rúveda EA. The Michael-Aldol condensation approach to the construction of key intermediates in the synthesis of terpenoid natural products Pure and Applied Chemistry. 68: 683-686. DOI: 10.1351/Pac199668030683 |
0.321 |
|
| 1996 |
Bacigaluppo JA, Colombo MI, Preite MD, Zinczuk J, Rúveda EA. The Michael-Aldol Condensation Approach to the Construction of Key Intermediates in the Synthesis of Nimbolide and Nagilactone A Synthetic Communications. 26: 2737-2749. DOI: 10.1080/00397919608004591 |
0.372 |
|
| 1996 |
Bacigaluppo J, Colombo MI, Preite MD, Zinczuk J, Rúveda EA, Sieler J. Enantioselective syntheses and resolution of the key white intermediate for the synthesis of trisporic acids Tetrahedron: Asymmetry. 7: 1041-1057. DOI: 10.1016/0957-4166(96)00109-7 |
0.391 |
|
| 1994 |
Bacigaluppo JA, Colombo MI, Cravero RM, González-Sierra M, Preite MD, Zinczuk J, Rúveda EA. Enantioselective synthesis of the white key intermediate for the synthesis of trisporic acids Tetrahedron: Asymmetry. 5: 1877-1880. DOI: 10.1016/S0957-4166(00)86255-2 |
0.712 |
|
| 1993 |
Bacigaluppo JA, Colombo MI, González-Sierra M, Preite MD, Zinczuk J, Rúveda EA, Duddeck H, Hiegemann M. Synthetic and structural studies of key intermediates toward forskolin and/or erigerol. Relative stereochemistry, conformational preferences and stereoselectivity control Journal of the Chemical Society-Perkin Transactions 1. 2009-2015. DOI: 10.1039/P19930002009 |
0.355 |
|
| 1993 |
Preite MD, Zinczuk J, Colombo MI, Bacigaluppo JA, González-Sierra M, Rúveda EA. Resolution and absolute configuration of a tricyclic lactone. A potentially useful precursor of highly functionalized terpenoids Tetrahedron: Asymmetry. 4: 17-20. DOI: 10.1016/S0957-4166(00)86006-1 |
0.319 |
|
| 1991 |
Bacigaluppo JA, Colombo MI, Zinczuk J, Huber SN, Mischne MP, Rúveda EA. Convenient and Short Route to a Key Intermediate in the Synthesis of Forskolin Synthetic Communications. 21: 1361-1367. DOI: 10.1080/00397919108021283 |
0.69 |
|
| 1991 |
Zinczuk J, Bacigaluppo JA, Mischne MP, Colombo MI, Rúveda EA. AN IMPROVED PREPARATION OF A TRICYCLIC LACTONE, A POTENTIALLY USEFUL PRECURSOR OF HIGHLY FUNCTIONALIZED TERPENOIDS Organic Preparations and Procedures International. 23: 392-394. DOI: 10.1080/00304949109458220 |
0.667 |
|
| 1990 |
Colombo MI, Zinczuk J, Bacigaluppo JA, Somoza C, Ruveda EA. Synthesis of the Ziegler key intermediate and related precursors for the synthesis of forskolin and erigerol The Journal of Organic Chemistry. 55: 5631-5639. DOI: 10.1021/Jo00308A023 |
0.35 |
|
| 1990 |
Colombo MI, Somoza C, Zinczuk J, Bacigaluppo JA, Rúveda EA. A practical and efficient synthesis of the ziegler key intermediate for the synthesis of forskolin Tetrahedron Letters. 31: 39-42. DOI: 10.1016/S0040-4039(00)94328-4 |
0.362 |
|
| 1990 |
Colombo MI, Signorella S, P.Mischne M, Gonzalez-Sierra M, Ruveda EA. Manganese (III) acetate and lewis acid mediated cyclization of olefinic β-keto esters; a comparative study Tetrahedron. 46: 4149-4154. DOI: 10.1016/S0040-4020(01)86750-8 |
0.346 |
|
| 1990 |
COLOMBO MI, SIGNORELLA S, MISCHNE MP, GONZALEZ-SIERRA M, RUVEDA EA. ChemInform Abstract: Manganese(III) Acetate and Lewis Acid Mediated Cyclization of Olefinic β-Keto Esters: A Comparative Study. Cheminform. 21. DOI: 10.1002/chin.199040083 |
0.667 |
|
| 1989 |
González-Sierra M, Olivieri AC, Colombo MI, Rúveda EA. Absolute stereochemistry of the novel dioxaspiro diterpenoids strictanonic and grindelistrictic acids. Stereoselective synthesis of strictanonic acid methyl ester and its C-6 epimer Journal of the Chemical Society-Perkin Transactions 1. 1393-1399. DOI: 10.1039/P19890001393 |
0.562 |
|
| 1989 |
GONZALEZ-SIERRA M, OLIVIERI AC, COLOMBO MI, RUVEDA EA. ChemInform Abstract: Absolute Stereochemistry of the Novel Dioxaspiro Diterpenoids Strictanonic and Grindelistrictic Acids. Stereoselective Synthesis of Strictanonic Acid Methyl Ester and Its C-6 Epimer. Cheminform. 20. DOI: 10.1002/chin.198949274 |
0.507 |
|
| 1987 |
Somoza C, Colombo MI, Olivieri AC, González-Sierra M, Rúveda EA. Model Studies for the Synthesis of Erigerol Synthesis of 1-Deoxy-13-Epierigerol from Grindelic Acid Synthetic Communications. 17: 1727-1733. DOI: 10.1080/00397918708063991 |
0.567 |
|
| 1986 |
Colombo MI, Bustos DA, Gonzalez-Sierra M, Olivieri AC, Ruveda EA. An extension of the Beierbeck and Saunders parameters for the semiempirical calculation of the 13C nuclear magnetic resonance chemical shifts: the gauche-γ(X) effect in epoxides Canadian Journal of Chemistry. 64: 552-555. DOI: 10.1139/V86-088 |
0.487 |
|
| 1985 |
Sierra MG, Olivieri AC, Colombo MI, Ruveda EA. Stereoselective synthesis of (+)-strictanonic acid, the enantiomer of a new type of diterpenoid, isolated from Grindelia stricta and Chrysothamnus paniculatus Journal of the Chemical Society, Chemical Communications. 1045-1046. DOI: 10.1039/C39850001045 |
0.76 |
|
| 1985 |
GONZALEZ SIERRA M, OLIVIERI AC, COLOMBO MI, RUVEDA EA. ChemInform Abstract: STEREOSELECTIVE SYNTHESIS OF (+)-STRICTANONIC ACID, THE ENANTIOMER OF A NEW TYPE OF DITERPENOID, ISOLATED FROM GRINDELIA STRICTA AND CHRYSOTHAMNUS PANICULATUS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198548312 |
0.542 |
|
| 1985 |
GONZALEZ SIERRA M, COLOMBO MI, OLIVIERI AC, ZUDENIGO ME, RUVEDA EA. ChemInform Abstract: STEREOSPECIFIC TRANSFORMATION OF GRINDELIC ACID INTO THE ANTIFEEDANT 6α-HYDROXYGRINDELIC ACID, ITS 6β-EPIMER, AND OTHER RELATED NATURAL DITERPENE ACIDS Chemischer Informationsdienst. 16. DOI: 10.1002/Chin.198519314 |
0.51 |
|
| 1984 |
Gonzalez Sierra M, Colombo MI, Olivieri AC, Zudenigo ME, Ruveda EA. Stereospecific transformation of grindelic acid into the antifeedant 6.alpha.-hydroxygrindelic acid, its 6.beta.-epimer, and other related natural diterpene acids The Journal of Organic Chemistry. 49: 4984-4988. DOI: 10.1021/Jo00199A045 |
0.512 |
|
| 1984 |
Sierra MG, Colombo MI, Zudenigo ME, Rúveda EA. 13C NMR spectral analysis of grindelane diterpenoid acids Phytochemistry. 23: 1685-1688. DOI: 10.1016/S0031-9422(00)83469-X |
0.75 |
|
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