| Year |
Citation |
Score |
| 2025 |
Leino TO, Bannykh A, Eskelinen T, Belyaev A, Pihko PM. Amino-Substituted 1,3-Diazaazulenes: Synthesis, Structural Studies, Reactivity, and Photophysical Properties. Chemistry (Weinheim An Der Bergstrasse, Germany). e202500861. PMID 40145878 DOI: 10.1002/chem.202500861 |
0.755 |
|
| 2024 |
Nechaev AA, Gonzalez G, Verma P, Peshkov VA, Bannykh A, Hashemi A, Hannonen J, Hamza A, Papai I, Laasonen K, Peljo P, Pihko PM. Exploration of Vitamin B6-Based Redox-Active Pyridinium Salts towards the Application in Aqueous Organic Flow Batteries. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400828. PMID 38640462 DOI: 10.1002/chem.202400828 |
0.726 |
|
| 2024 |
Bannykh A, Pihko PM. Carboxylate-Catalyzed -Silylation of Terminal Alkynes. Organic Letters. PMID 38428925 DOI: 10.1021/acs.orglett.3c04213 |
0.769 |
|
| 2023 |
Riuttamäki S, Bannykh A, Pihko PM. Carboxylate Catalysis: A Catalytic -Silylative Aldol Reaction of Aldehydes and Ethyl Diazoacetate. The Journal of Organic Chemistry. 88: 14396-14403. PMID 37768196 DOI: 10.1021/acs.joc.3c01304 |
0.77 |
|
| 2022 |
Riuttamäki S, Laczkó G, Madarász Á, Földes T, Pápai I, Bannykh A, Pihko PM. Carboxylate Catalyzed Isomerization of β,γ-Unsaturated N-Acetylcysteamine Thioesters. Chemistry (Weinheim An Der Bergstrasse, Germany). e202201030. PMID 35604200 DOI: 10.1002/chem.202201030 |
0.74 |
|
| 2020 |
Csókás D, Siitonen JH, Pihko PM, Pápai I. Conformationally Locked Pyramidality Explains the Diastereoselectivity in the Methylation of -Fused Butyrolactones. Organic Letters. PMID 32338517 DOI: 10.1021/Acs.Orglett.0C01008 |
0.733 |
|
| 2020 |
Kortet S, Claraz A, Pihko PM. Catalytic Enantioselective Total Synthesis of (+)-Lycoperdic Acid. Organic Letters. PMID 32216321 DOI: 10.1021/Acs.Orglett.0C00772 |
0.41 |
|
| 2019 |
Neuvonen AJ, Noutsias D, Topić F, Rissanen K, Földes T, Pápai I, Pihko PM. Dynamic Refolding of Ion-Pair Catalysts in Response to Different Anions. The Journal of Organic Chemistry. PMID 31536339 DOI: 10.1021/Acs.Joc.9B01980 |
0.337 |
|
| 2018 |
Pihko P, Kärki K, Siitonen J, Kortet S, Cederström M. Enzymatic Resolution of 3-oxodicyclopentadiene on a Decagram Scale Synlett. 29: 1723-1728. DOI: 10.1055/S-0037-1610109 |
0.715 |
|
| 2017 |
Földes T, Madarász Á, Révész Á, Dobi Z, Varga S, Hamza A, Nagy PR, Pihko PM, Pápai I. Stereocontrol in Diphenylprolinol Silyl Ether Catalyzed Michael Additions: Steric Shielding or Curtin-Hammett Scenario? Journal of the American Chemical Society. PMID 29088911 DOI: 10.1021/Jacs.7B07097 |
0.469 |
|
| 2017 |
Pihko P, Mäkinen M, Mallik R, Siitonen J, Kärki K. Towards Waltheriones C and D: Synthesis of the Oxabicyclic Core Synlett. 28: 1209-1213. DOI: 10.1055/S-0036-1588150 |
0.739 |
|
| 2017 |
Neuvonen AJ, Földes T, Madarász Á, Pápai I, Pihko PM. Organocatalysts Fold To Generate an Active Site Pocket for the Mannich Reaction Acs Catalysis. 7: 3284-3294. DOI: 10.1021/Acscatal.7B00336 |
0.411 |
|
| 2016 |
Tuokko S, Pihko PM, Honkala K. First Principles Calculations for Hydrogenation of Acrolein on Pd and Pt: Chemoselectivity Depends on Steric Effects on the Surface. Angewandte Chemie (International Ed. in English). 55: 1670-4. PMID 26791881 DOI: 10.1002/Anie.201507631 |
0.39 |
|
| 2016 |
Pihko P, Tuokko S. Palladium on Charcoal Catalyzed 3,4-Hydroperoxidation of α-Substituted Enals with Triethylsilane and Water Synlett. 27: 1649-1652. DOI: 10.1055/S-0035-1561633 |
0.383 |
|
| 2016 |
List B, Shevchenko GA, Claraz A, Sahoo G, Berta D, Madarász Á, Pápai I, Pihko PM. Enantioselective Construction of Tertiary Stereocenters Synfacts. 12: 198-198. DOI: 10.1055/S-0035-1561123 |
0.327 |
|
| 2016 |
Tuokko S, Honkala K, Pihko PM. Pd/C-Catalyzed Hydrosilylation of Enals and Enones with Triethylsilane: Conformer Populations Control the Stereoselectivity Acs Catalysis. 7: 480-493. DOI: 10.1021/Acscatal.6B02856 |
0.432 |
|
| 2016 |
Vijayan A, Baiju TV, Jijy E, Prakash P, Shimi M, Joseph N, Pihko PM, Varughese S, Radhakrishnan KV. An easy access to fused chromanones via rhodium catalyzed oxidative coupling of salicylaldehydes with heterobicyclic olefins Tetrahedron. 72: 4007-4015. DOI: 10.1016/J.Tet.2016.05.031 |
0.381 |
|
| 2015 |
Claraz A, Sahoo G, Berta D, Madarász Á, Pápai I, Pihko PM. A Catalyst Designed for the Enantioselective Construction of Methyl- and Alkyl-Substituted Tertiary Stereocenters. Angewandte Chemie (International Ed. in English). PMID 26603376 DOI: 10.1002/Anie.201509302 |
0.449 |
|
| 2015 |
Onwukwe GU, Koski MK, Pihko P, Schmitz W, Wierenga RK. Structures of yeast peroxisomal Δ(3),Δ(2)-enoyl-CoA isomerase complexed with acyl-CoA substrate analogues: the importance of hydrogen-bond networks for the reactivity of the catalytic base and the oxyanion hole. Acta Crystallographica. Section D, Biological Crystallography. 71: 2178-91. PMID 26527136 DOI: 10.1107/S139900471501559X |
0.308 |
|
| 2014 |
Neuvonen AJ, Pihko PM. Enantioselective Mannich reaction of β-keto esters with aromatic and aliphatic imines using a cooperatively assisted bifunctional catalyst. Organic Letters. 16: 5152-5. PMID 25229423 DOI: 10.1021/Ol5025025 |
0.424 |
|
| 2014 |
Kemppainen EK, Sahoo G, Piisola A, Hamza A, Kótai B, Pápai I, Pihko PM. Mukaiyama-Michael reactions with trans-2,5-diarylpyrrolidine catalysts: enantioselectivity arises from attractive noncovalent interactions, not from steric hindrance. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 5983-93. PMID 24692273 DOI: 10.1002/Chem.201304240 |
0.432 |
|
| 2014 |
Leskinen MV, Madarász Á, Yip KT, Vuorinen A, Pápai I, Neuvonen AJ, Pihko PM. Cross-dehydrogenative couplings between indoles and β-keto esters: ligand-assisted ligand tautomerization and dehydrogenation via a proton-assisted electron transfer to Pd(II). Journal of the American Chemical Society. 136: 6453-62. PMID 24684203 DOI: 10.1021/Ja501681Y |
0.35 |
|
| 2014 |
Siitonen JH, Pihko PM. Total synthesis of (+)-Greek tobacco lactone Synlett. 25: 1888-1890. DOI: 10.1055/S-0034-1378273 |
0.76 |
|
| 2014 |
Tuokko S, Pihko PM. Palladium on charcoal as a catalyst for stoichiometric chemo- and stereoselective hydrosilylations and hydrogenations with triethylsilane Organic Process Research and Development. 18: 1740-1751. DOI: 10.1021/Op5003209 |
0.388 |
|
| 2014 |
Moilanen J, Neuvonen A, Pihko P. Reaction mechanism of an intramolecular oxime transfer reaction: A computational study Journal of Organic Chemistry. 79: 2006-2014. DOI: 10.1021/Jo402676Z |
0.364 |
|
| 2013 |
Jijy E, Prakash P, Shimi M, Pihko PM, Joseph N, Radhakrishnan KV. Rhodium catalyzed oxidative coupling of salicylaldehydes with diazabicyclic olefins: a one pot strategy involving aldehyde C-H cleavage and π-allyl chemistry towards the synthesis of fused ring chromanones. Chemical Communications (Cambridge, England). 49: 7349-51. PMID 23846351 DOI: 10.1039/C3Cc43485K |
0.445 |
|
| 2013 |
Prakash P, Jijy E, Preethanuj P, Pihko PM, Sarath Chand S, Radhakrishnan KV. Palladium-catalyzed skeletal rearrangement of spirotricyclic olefins: a facile one-pot strategy for the synthesis of a novel motif with cyclopentene fused to benzofuran and pyrazolidine. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 10473-7. PMID 23788444 DOI: 10.1002/Chem.201301475 |
0.438 |
|
| 2013 |
Nimje RY, Leskinen MV, Pihko PM. A three-component palladium-catalyzed oxidative C-C coupling reaction: a domino process in two dimensions. Angewandte Chemie (International Ed. in English). 52: 4818-22. PMID 23553956 DOI: 10.1002/Anie.201300833 |
0.389 |
|
| 2013 |
Joseph N, Rajan R, John J, Devika NV, Chand SS, Suresh E, Pihko PM, Radhakrishnan KV. An exclusive approach to 3,4-disubstituted cyclopentenes and alkylidene cyclopentenes via the palladium catalyzed ring opening of azabicyclic olefins with aryl halides Rsc Advances. 3: 7751-7757. DOI: 10.1039/C3Ra41504J |
0.451 |
|
| 2013 |
Jijy E, Prakash P, Shimi M, Saranya S, Preethanuj P, Pihko PM, Varughese S, Radhakrishnan KV. Rhodium(III)-catalyzed ring-opening of strained olefins through C-H activation of O-acetyl ketoximes: An efficient synthesis of trans-functionalized cyclopentenes and spiro[2.4]heptenes Tetrahedron Letters. 54: 7127-7131. DOI: 10.1016/J.Tetlet.2013.10.089 |
0.407 |
|
| 2012 |
Sahoo G, Rahaman H, Madarász A, Pápai I, Melarto M, Valkonen A, Pihko PM. Dihydrooxazine oxides as key intermediates in organocatalytic Michael additions of aldehydes to nitroalkenes. Angewandte Chemie (International Ed. in English). 51: 13144-8. PMID 23150243 DOI: 10.1002/Anie.201204833 |
0.396 |
|
| 2012 |
Yip KT, Nimje RY, Leskinen MV, Pihko PM. Palladium-catalyzed dehydrogenative β'-arylation of β-keto esters under aerobic conditions: interplay of metal and Brønsted acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 12590-4. PMID 22915444 DOI: 10.1002/Chem.201201988 |
0.352 |
|
| 2012 |
Probst N, Madarász A, Valkonen A, Pápai I, Rissanen K, Neuvonen A, Pihko PM. Cooperative assistance in bifunctional organocatalysis: enantioselective Mannich reactions with aliphatic and aromatic imines. Angewandte Chemie (International Ed. in English). 51: 8495-9. PMID 22777736 DOI: 10.1002/Anie.201203852 |
0.407 |
|
| 2012 |
Leskinen MV, Yip KT, Valkonen A, Pihko PM. Palladium-catalyzed dehydrogenative β'-functionalization of β-keto esters with indoles at room temperature. Journal of the American Chemical Society. 134: 5750-3. PMID 22424139 DOI: 10.1021/Ja300684R |
0.38 |
|
| 2012 |
Kemppainen EK, Sahoo G, Valkonen A, Pihko PM. Mukaiyama-Michael reactions with acrolein and methacrolein: a catalytic enantioselective synthesis of the C17-C28 fragment of pectenotoxins. Organic Letters. 14: 1086-9. PMID 22296172 DOI: 10.1021/Ol203486P |
0.474 |
|
| 2012 |
Himanen JA, Pihko PM. Synthesis of trisaccharides by hetero-diels-alder welding of two monosaccharide units European Journal of Organic Chemistry. 3765-3780. DOI: 10.1002/Ejoc.201200277 |
0.467 |
|
| 2011 |
Benohoud M, Tuokko S, Pihko PM. Stereoselective hydrosilylation of enals and enones catalysed by palladium nanoparticles. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 8404-13. PMID 21744402 DOI: 10.1002/Chem.201100655 |
0.364 |
|
| 2011 |
Venkatesan R, Alahuhta M, Pihko PM, Wierenga RK. High resolution crystal structures of triosephosphate isomerase complexed with its suicide inhibitors: the conformational flexibility of the catalytic glutamate in its closed, liganded active site. Protein Science : a Publication of the Protein Society. 20: 1387-97. PMID 21633986 DOI: 10.1002/Pro.667 |
0.323 |
|
| 2011 |
Rahaman H, Madarász A, Pápai I, Pihko PM. Dual hydrogen-bond/enamine catalysis enables a direct enantioselective three-component domino reaction. Angewandte Chemie (International Ed. in English). 50: 6123-7. PMID 21604346 DOI: 10.1002/Anie.201101835 |
0.345 |
|
| 2011 |
Pápai I, Hamza A, Pihko PM, Wierenga RK. Stereoelectronic requirements for optimal hydrogen-bond-catalyzed enolization. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 2859-66. PMID 21308811 DOI: 10.1002/Chem.201002943 |
0.308 |
|
| 2011 |
Aho JE, Piisola A, Syam Krishnan K, Pihko PM. Synthetic studies towards pectenotoxin-2: Synthesis of the nonanomeric 10-epi-ABCDE ring segment by kinetic spiroketalization European Journal of Organic Chemistry. 1682-1694. DOI: 10.1002/Ejoc.201001411 |
0.463 |
|
| 2011 |
Benohoud M, Erkkilä A, Pihko PM. Organocatalytic α‐Methylenation of Aldehydes: Preparation of 3,7‐Dimethyl‐2‐Methylene‐6‐Octenal Organic Syntheses. 201-208. DOI: 10.1002/0471264229.Os087.22 |
0.423 |
|
| 2010 |
Pihko PM, Majander I, Erkkilä A. Enamine catalysis. Topics in Current Chemistry. 291: 29-75. PMID 21494950 DOI: 10.1007/978-3-642-02815-1_21 |
0.331 |
|
| 2010 |
Pohjakallio A, Pihko PM, Liu J. Base-catalyzed isomerization of 2-isoxazolines enables a two-step enantioselective synthesis of β-hydroxynitriles from enals. The Journal of Organic Chemistry. 75: 6712-5. PMID 20825148 DOI: 10.1021/Jo1013788 |
0.468 |
|
| 2010 |
Pohjakallio A, Pihko PM, Laitinen UM. Synthesis of 2-isoxazolines: enantioselective and racemic methods based on conjugate additions of oximes. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 11325-39. PMID 20726019 DOI: 10.1002/Chem.201000861 |
0.454 |
|
| 2010 |
Pihko P, Pohjakallio A, Laitinen U. Synthesis of 2-Isoxazolines via Conjugate Additions Synfacts. 2010: 1226-1226. DOI: 10.1055/S-0030-1258761 |
0.394 |
|
| 2010 |
Al-Hunaiti A, Niemi T, Sibaouih A, Pihko P, Leskelä M, Repo T. Solvent free oxidation of primary alcohols and diols using thymine iron(iii) catalyst Chemical Communications. 46: 9250-9252. DOI: 10.1039/C0Cc04043F |
0.332 |
|
| 2010 |
Nicolaou KC, Pihko PM, Diedrichs N, Zou N, Bernal F. ChemInform Abstract: Synthesis of the FGHI Ring System of Azaspiracid. Cheminform. 32: no-no. DOI: 10.1002/chin.200129197 |
0.42 |
|
| 2009 |
Pohjakallio A, Pihko PM. Enantioselective synthesis of 2-isoxazolines by a one-flask conjugate addition/oxime-transfer process. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 3960-4. PMID 19263445 DOI: 10.1002/Chem.200802684 |
0.431 |
|
| 2008 |
Helmboldt H, Aho JE, Pihko PM. Synthetic studies toward pectenotoxin 2. Part II. Synthesis of the CDE and CDEF ring systems. Organic Letters. 10: 4183-5. PMID 18763803 DOI: 10.1021/Ol801585J |
0.351 |
|
| 2008 |
Aho JE, Salomäki E, Rissanen K, Pihko PM. Synthetic studies toward pectenotoxin 2. Part I. Stereocontrolled access to the C10-C22 fragment. Organic Letters. 10: 4179-82. PMID 18763802 DOI: 10.1021/Ol8015868 |
0.366 |
|
| 2008 |
Pohjakallio A, Pihko PM. A versatile entry to 3-unsubstituted 2-isoxazolines Synlett. 827-830. DOI: 10.1055/S-2008-1042900 |
0.369 |
|
| 2007 |
Castagnolo D, Breuer I, Pihko PM. Direct kinetic formation of nonanomeric [6.5]-spiroketals in aqueous media. The Journal of Organic Chemistry. 72: 10081-7. PMID 18004871 DOI: 10.1021/Jo702022U |
0.382 |
|
| 2007 |
Lahtinen P, Ahmad JU, Lankinen E, Pihko P, Leskelä M, Repo T. Organocatalyzed oxidation of alcohols to aldehydes with molecular oxygen Journal of Molecular Catalysis a: Chemical. 275: 228-232. DOI: 10.1016/J.Molcata.2007.06.001 |
0.32 |
|
| 2007 |
Erkkilä A, Pihko PM. Rapid organocatalytic aldehyde-aldehyde condensation reactions European Journal of Organic Chemistry. 4205-4216. DOI: 10.1002/Ejoc.200700292 |
0.411 |
|
| 2007 |
Erkkilä A, Pihko PM, Clarke MR. Simple primary anilines as iminium catalysts for the epoxidation of α-substituted acroleins Advanced Synthesis and Catalysis. 349: 802-806. DOI: 10.1002/Adsc.200700048 |
0.41 |
|
| 2006 |
Erkkilä A, Pihko PM. Mild organocatalytic alpha-methylenation of aldehydes. The Journal of Organic Chemistry. 71: 2538-41. PMID 16526814 DOI: 10.1021/Jo052529Q |
0.343 |
|
| 2006 |
Nicolaou KC, Chen DY, Li Y, Uesaka N, Petrovic G, Koftis TV, Bernal F, Frederick MO, Govindasamy M, Ling T, Pihko PM, Tang W, Vyskocil S. Total synthesis and structural elucidation of azaspiracid-1. Synthesis-based analysis of originally proposed structures and indication of their non-identity to the natural product. Journal of the American Chemical Society. 128: 2258-67. PMID 16478179 DOI: 10.1021/Ja054748Z |
0.755 |
|
| 2006 |
Nicolaou KC, Pihko PM, Bernal F, Frederick MO, Qian W, Uesaka N, Diedrichs N, Hinrichs J, Koftis TV, Loizidou E, Petrovic G, Rodriquez M, Sarlah D, Zou N. Total synthesis and structural elucidation of azaspiracid-1. Construction of key building blocks for originally proposed structure. Journal of the American Chemical Society. 128: 2244-57. PMID 16478178 DOI: 10.1021/Ja0547477 |
0.752 |
|
| 2006 |
Pihko PM, Laurikainen KM, Usano A, Nyberg AI, Kaavi JA. Effect of additives on the proline-catalyzed ketone-aldehyde aldol reactions Tetrahedron. 62: 317-328. DOI: 10.1016/J.Tet.2005.09.070 |
0.416 |
|
| 2005 |
Källström S, Erkkilä A, Pihko PM, Sjöholm R, Sillanpää R, Leino R. Consecutive proline-catalyzed aldol reactions and metal-mediated allylations: Rapid entries to polypropionates Synlett. 751-756. DOI: 10.1055/S-2005-864791 |
0.373 |
|
| 2005 |
Piispanen PS, Pihko PM. Direct synthesis of N-substituted, functionalized aspartic acids using alkali maleates and amines Tetrahedron Letters. 46: 2751-2755. DOI: 10.1016/J.Tetlet.2005.02.159 |
0.354 |
|
| 2004 |
Pihko PM, Aho JE. Access to both anomers of pectenotoxin spiroketals by kinetic spiroketalization. Organic Letters. 6: 3849-52. PMID 15469365 DOI: 10.1021/Ol048321T |
0.431 |
|
| 2004 |
Pihko PM, Pohjakallio A. Enantioselective organocatalytic diels aminations: α-aminations of cyclic β-keto esters and β-keto lactones with cinchonidine and cinchonine Synlett. 2115-2118. DOI: 10.1055/S-2004-831326 |
0.386 |
|
| 2004 |
Nyberg AI, Usano A, Pihko PM. Proline-catalyzed ketone-aldehyde aldol reactions are accelerated by water Synlett. 1891-1896. DOI: 10.1055/S-2004-831296 |
0.381 |
|
| 2004 |
Pihko PM, Rissa TK, Aksela R. Enantiospecific synthesis of isomers of AES, a new environmentally friendly chelating agent Tetrahedron. 60: 10949-10954. DOI: 10.1016/J.Tet.2004.09.024 |
0.33 |
|
| 2003 |
Pihko PM, Salo TM. Excess sodium ions improve Z selectivity in Horner-Wadsworth-Emmons olefinations with the Ando phosphonate Tetrahedron Letters. 44: 4361-4364. DOI: 10.1016/S0040-4039(03)00935-3 |
0.301 |
|
| 2003 |
Pihko PM, Erkkilä A. Enantioselective synthesis of prelactone B using a proline-catalyzed crossed-aldol reaction Tetrahedron Letters. 44: 7607-7609. DOI: 10.1016/J.Tetlet.2003.08.060 |
0.449 |
|
| 2002 |
Selkälä SA, Tois J, Pihko PM, Koskinen AMP. Asymmetric Organocatalytic Diels-Alder Reactions on Solid Support Advanced Synthesis and Catalysis. 344: 941-945. DOI: 10.1002/1615-4169(200210)344:9<941::Aid-Adsc941>3.0.Co;2-M |
0.356 |
|
| 2002 |
Koskinen A, Pihko P. Laboratoriotyöt integroidaan luentoihin: Teknillisen korkeakoulun orgaanisen kemian laboratorio pyrkii Euroopan kärkiviisikkoon Kemia-Kemi/Finnish Chemical Journal. 29: 31-33. |
0.569 |
|
| 2001 |
Nicolaou KC, Qian W, Bernal F, Uesaka N, Pihko PM, Hinrichs J. Synthesis of the ABCD Ring System of Azaspiracid. Angewandte Chemie (International Ed. in English). 40: 4068-4071. PMID 29712267 DOI: 10.1002/1521-3773(20011105)40:21<4068::AID-ANIE4068>3.0.CO;2-Y |
0.65 |
|
| 2001 |
Nicolaou KC, Qian W, Bernal F, Uesaka N, Pihko PM, Hinrichs J. Synthesis of the ABCD Ring System of Azaspiracid We thank Drs. D. H. Huang and G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supported by the National Institutes of Health (USA), The Skaggs Institute for Chemical Biology, a predoctoral fellowship from Bristol-Myers Squibb (to F.B.), postdoctoral fellowships from The Skaggs Institute for Research (to W.Q.), the Academy of Finland, the Ella and Georg Ehrnrooth Foundation and the Tauno Tönning Foundation (all to P.M.P.), and Bayer AG (to J.H.), as well as grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-La Roche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 40: 4068-4071. PMID 12404495 DOI: 10.1002/1521-3773(20011105)40:21<4068::AID-ANIE4068>3.0.CO;2-Y |
0.598 |
|
| 2001 |
Nicolaou KC, Pihko PM, Diedrichs N, Zou N, Bernal F. Synthesis of the FGHI Ring System of Azaspiracid We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from Bristol-Myers Squibb (F.B.), postdoctoral fellowships from the Academy of Finland, the Ella and Georg Ehrnrooth Foundation, and the Tauno Tönning Foundation (all to P.M.P.), ArrayBiopharma (N.Z.), and Bayer AG (N.D.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 40: 1573. PMID 11353466 DOI: 10.1002/1521-3773(20010504)40:9<1573::AID-ANIE15733>3.0.CO;2-D |
0.607 |
|
| 2001 |
Nicolaou KC, Pihko PM, Diedrichs N, Zou N, Bernal F. Synthesis of the FGHI Ring System of Azaspiracid We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. Financial support for this work was provided by The Skaggs Institute for Chemical Biology, the National Institutes of Health (USA), a predoctoral fellowship from Bristol-Myers Squibb (F.B.), postdoctoral fellowships from the Academy of Finland, the Ella and Georg Ehrnrooth Foundation, and the Tauno Tönning Foundation (all to P.M.P.), ArrayBiopharma (N.Z.), and Bayer AG (N.D.), and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-LaRoche, DuPont, Merck, Novartis, Pfizer, and Schering Plough. Angewandte Chemie (International Ed. in English). 40: 1262-1265. PMID 11301444 DOI: 10.1002/1521-3773(20010401)40:7<1262::Aid-Anie1262>3.0.Co;2-9 |
0.672 |
|
| 1999 |
Pihko PM, Koskinen AMP. The triumph of zinc: A short and highly efficient synthesis of the calyculin C1-C9 tetraene building block by Negishi coupling Synlett. 1966-1968. DOI: 10.1055/S-1999-2979 |
0.364 |
|
| 1999 |
Pihko PM, Koskinen AMP, Nissinen MJ, Rissanen K. Formation of stable spiro[4.4] ortho ester aminals during the synthesis of the C26-C32 oxazole fragment of calyculin C Journal of Organic Chemistry. 64: 652-654. DOI: 10.1021/Jo981674J |
0.387 |
|
| 1998 |
Pihko PM, Koskinen AM. Synthesis of the C(26)-C(32) Oxazole Fragment of Calyculin C: A Test Case for Oxazole Syntheses. The Journal of Organic Chemistry. 63: 92-98. PMID 11674047 DOI: 10.1021/Jo971167M |
0.656 |
|
| 1997 |
Lindvall MK, Pihko PM, Koskinen AM. The binding mode of calyculin A to protein phosphatase-1. A novel spiroketal vector model. The Journal of Biological Chemistry. 272: 23312-6. PMID 9287341 DOI: 10.1074/Jbc.272.37.23312 |
0.607 |
|
| 1994 |
Koskinen AMP, Pihko PM. Calyculins. Asymmetric synthesis of the C26-C32 fragment Tetrahedron Letters. 35: 7417-7420. DOI: 10.1016/0040-4039(94)85330-4 |
0.355 |
|
| Show low-probability matches. |