| Year |
Citation |
Score |
| 2021 |
Soleymani Movahed F, Foo SW, Mori S, Ogawa S, Saito S. Phosphorus-Based Organocatalysis for the Dehydrative Cyclization of -(2-Hydroxyethyl)amides into 2-Oxazolines. The Journal of Organic Chemistry. PMID 34882422 DOI: 10.1021/acs.joc.1c02318 |
0.374 |
|
| 2020 |
Kamada K, Jung J, Taku W, Sekizawa K, Sato S, Morikawa T, Fukuzumi S, Saito S. Photocatalytic CO Reduction Using a Robust Multifunctional Iridium Complex towards the Selective Formation of Formic Acid. Journal of the American Chemical Society. PMID 32456417 DOI: 10.1021/Jacs.0C03097 |
0.326 |
|
| 2020 |
Yoshioka S, Jung J, Saito S. Development of Catalytic Reduction of Renewable Carbon Resources Using Well-Elaborated Organometallic Complexes with PNNP Tetradentate Ligands Journal of Synthetic Organic Chemistry Japan. 78: 856-866. DOI: 10.5059/Yukigoseikyokaishi.78.856 |
0.308 |
|
| 2020 |
Saito S, Movahed FS, Sawant DN, Bagal DB. Tris(o-phenylenedioxy)cyclotriphosphazene as a Promoter for the Formation of Amide Bonds Between Aromatic Acids and Amines Synthesis. 52: 3253-3262. DOI: 10.1055/S-0040-1707174 |
0.719 |
|
| 2019 |
Saito S, Hatanaka K, Yamamoto H. Asymmetric Mannich-Type Reactions of Aldimines with a Chiral Acetate. Organic Letters. 2: 1891-1894. PMID 10891184 DOI: 10.1021/Ol000099E |
0.516 |
|
| 2019 |
Saito A, Yoshioka S, Naruto M, Saito S. Catalytic Hydrogenation of N‐protected α‐Amino Acids Using Ruthenium Complexes with Monodentate Phosphine Ligands Advanced Synthesis & Catalysis. 362: 424-429. DOI: 10.1002/Adsc.201901298 |
0.347 |
|
| 2018 |
Wang LM, Kobayashi K, Arisawa M, Saito S, Naka H. Pd/TiO-Photocatalyzed Self-Condensation of Primary Amines To Afford Secondary Amines at Ambient Temperature. Organic Letters. PMID 30460855 DOI: 10.1021/Acs.Orglett.8B03271 |
0.354 |
|
| 2018 |
Yoshioka S, Saito S. Catalytic hydrogenation of carboxylic acids using low-valent and high-valent metal complexes. Chemical Communications (Cambridge, England). PMID 30311923 DOI: 10.1039/C8Cc06543H |
0.338 |
|
| 2018 |
Sawant DN, Bagal DB, Ogawa S, Selvam K, Saito S. Diboron-Catalyzed Dehydrative Amidation of Aromatic Carboxylic Acids with Amines. Organic Letters. PMID 30020789 DOI: 10.1021/Acs.Orglett.8B01480 |
0.731 |
|
| 2018 |
Wang LM, Morioka Y, Jenkinson K, Wheatley AEH, Saito S, Naka H. N-Alkylation of functionalized amines with alcohols using a copper-gold mixed photocatalytic system. Scientific Reports. 8: 6931. PMID 29720619 DOI: 10.1038/S41598-018-25293-Z |
0.41 |
|
| 2018 |
Takada Y, Caner J, Naka H, Saito S. Photocatalytic hydrogenolysis of allylic alcohols for rapid access to platform chemicals and fine chemicals Pure and Applied Chemistry. 90: 167-174. DOI: 10.1515/Pac-2017-0501 |
0.362 |
|
| 2018 |
Wang L, Jenkinson K, Wheatley AEH, Kuwata K, Saito S, Naka H. Photocatalytic N-Methylation of Amines over Pd/TiO2 for the Functionalization of Heterocycles and Pharmaceutical Intermediates Acs Sustainable Chemistry & Engineering. 6: 15419-15424. DOI: 10.1021/Acssuschemeng.8B03855 |
0.305 |
|
| 2017 |
Saito S, Takada Y, Caner J, Kaliyamoorthy S, Naka H. Photocatalytic transfer hydrogenolysis of allylic alcohols on Pd/TiO2: A Shortcut to (S)-(+)-lavandulol. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28972300 DOI: 10.1002/Chem.201704099 |
0.367 |
|
| 2017 |
Naruto M, Agrawal S, Toda K, Saito S. Catalytic transformation of functionalized carboxylic acids using multifunctional rhenium complexes. Scientific Reports. 7: 3425. PMID 28611423 DOI: 10.1038/S41598-017-03436-Y |
0.395 |
|
| 2017 |
Miura T, Naruto M, Toda K, Shimomura T, Saito S. Multifaceted catalytic hydrogenation of amides via diverse activation of a sterically confined bipyridine-ruthenium framework. Scientific Reports. 7: 1586. PMID 28512286 DOI: 10.1038/S41598-017-01645-Z |
0.389 |
|
| 2016 |
Takada Y, Iida M, Iida K, Miura T, Saito S. Versatile Ruthenium Complex “RuPCY” for Directed Catalytic Hydrogen Management in Organic Synthesis Journal of Synthetic Organic Chemistry, Japan. 74: 1078-1089. DOI: 10.5059/Yukigoseikyokaishi.74.1078 |
0.338 |
|
| 2016 |
Stefaowitz J, Schepmann D, Daniliuc C, Saito S, Wünsch B. Synthesis of morphan derivatives with additional substituents in 8-position Zeitschrift FüR Naturforschung B. 71: 1057-1069. DOI: 10.1515/Znb-2016-0129 |
0.33 |
|
| 2015 |
Naruto M, Saito S. Cationic mononuclear ruthenium carboxylates as catalyst prototypes for self-induced hydrogenation of carboxylic acids. Nature Communications. 6: 8140. PMID 26314266 DOI: 10.1038/Ncomms9140 |
0.422 |
|
| 2015 |
Matsuoka A, Isogawa T, Morioka Y, Knappett BR, Wheatley AEH, Saito S, Naka H. Hydration of nitriles to amides by a chitin-supported ruthenium catalyst Rsc Advances. 5: 12152-12160. DOI: 10.1039/C4Ra15682J |
0.39 |
|
| 2015 |
Schulte A, Janich S, Würthwein E, Saito S, Wünsch B. Investigation of the Corey Bromolactamization withN-Functionalized Allylamines Journal of Heterocyclic Chemistry. 53: 1827-1837. DOI: 10.1002/Jhet.2493 |
0.362 |
|
| 2015 |
Schulte A, Saito S, Wünsch B. Stereoselective Synthesis ofcis,cis-Configured Perhydroquinoxaline-5-Carbonitrile from Cyclohex-2-en-1-ol Journal of Heterocyclic Chemistry. 53: 533-536. DOI: 10.1002/Jhet.2322 |
0.323 |
|
| 2014 |
Takada Y, Foo SW, Yamazaki Y, Saito S. Catalytic fluoride triggers dehydrative oxazolidinone synthesis from CO2 Rsc Adv.. 4: 50851-50857. DOI: 10.1039/C4Ra09609F |
0.365 |
|
| 2014 |
Schulte A, Saito S, Wünsch B. Stereoselective Synthesis ofcis,cis-Configured Vicinal Triamines European Journal of Organic Chemistry. 2014: 5749-5756. DOI: 10.1002/Ejoc.201402685 |
0.365 |
|
| 2013 |
Iida K, Miura T, Ando J, Saito S. The dual role of ruthenium and alkali base catalysts in enabling a conceptually new shortcut to N-unsubstituted pyrroles through unmasked α-amino aldehydes. Organic Letters. 15: 1436-9. PMID 23470156 DOI: 10.1021/Ol4001262 |
0.419 |
|
| 2013 |
Foo SW, Takada Y, Yamazaki Y, Saito S. Dehydrative synthesis of chiral oxazolidinones catalyzed by alkali metal carbonates under low pressure of CO2 Tetrahedron Letters. 54: 4717-4720. DOI: 10.1016/J.Tetlet.2013.06.100 |
0.391 |
|
| 2013 |
Miura T, Held IE, Oishi S, Naruto M, Saito S. Catalytic hydrogenation of unactivated amides enabled by hydrogenation of catalyst precursor Tetrahedron Letters. 54: 2674-2678. DOI: 10.1016/J.Tetlet.2013.03.047 |
0.397 |
|
| 2013 |
Foo SW, Oishi S, Saito S. ChemInform Abstract: Aldol Condensation of Amides Using Phosphazene-Based Catalysis. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201301070 |
0.303 |
|
| 2012 |
Foo SW, Oishi S, Saito S. Aldol condensation of amides using phosphazene-based catalysis Tetrahedron Letters. 53: 5445-5448. DOI: 10.1016/J.Tetlet.2012.07.129 |
0.492 |
|
| 2011 |
Du Y, Oishi S, Saito S. Selective N-alkylation of amines with alcohols by using non-metal-based acid-base cooperative catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 12262-7. PMID 21938751 DOI: 10.1002/Chem.201102446 |
0.319 |
|
| 2011 |
Goto A, Naka H, Noyori R, Saito S. One-pot nitrile aldolization/hydration operation giving β-hydroxy carboxamides. Chemistry, An Asian Journal. 6: 1740-3. PMID 21416618 DOI: 10.1002/Asia.201000921 |
0.531 |
|
| 2011 |
Zhao Y, Foo SW, Saito S. Iron/amino acid catalyzed direct N-alkylation of amines with alcohols. Angewandte Chemie (International Ed. in English). 50: 3006-9. PMID 21404386 DOI: 10.1002/Anie.201006660 |
0.317 |
|
| 2011 |
Goto A, Naka H, Noyori R, Saito S. ChemInform Abstract: One-Pot Nitrile Aldolization/Hydration Operation Giving β-Hydroxy Carboxamides. Cheminform. 42: no-no. DOI: 10.1002/chin.201144058 |
0.492 |
|
| 2010 |
Kose O, Saito S. Cross-coupling reaction of alcohols for carbon-carbon bond formation using pincer-type NHC/palladium catalysts. Organic & Biomolecular Chemistry. 8: 896-900. PMID 20135049 DOI: 10.1039/B914618K |
0.384 |
|
| 2010 |
Saito S, Hatanaka K, Yamamoto H. ChemInform Abstract: Nucleophilic Addition of Organomagnesiums to Aldimines: Scandium Triflate (Sc(OTf)3) as an Effective Catalyst. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200213096 |
0.313 |
|
| 2010 |
Saito S, Nagahara T, Yamamoto H. ChemInform Abstract: Efficient Dehydration of Hydroxyenals and -enones: HfCl4×(THF)2 as an Effective Catalyst for Di-, Tri- and Tetraene Formation. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200208058 |
0.324 |
|
| 2010 |
Saito S, Nakadai M, Yamamoto H. ChemInform Abstract: Diamine-Protonic Acid Catalysts for Catalytic Asymmetric Aldol Reaction. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200145045 |
0.383 |
|
| 2010 |
Saito S, Hatanaka K, Yamamoto H. ChemInform Abstract: Asymmetric Mannich-Type Reactions with a Chiral Acetate: Effect of Lewis Acid on Activation of Aldimine. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200121024 |
0.35 |
|
| 2010 |
Saito S, Kano T, Muto H, Nakadai M, Yamamoto H. ChemInform Abstract: Asymmetric Coupling of Phenols with Arylleads. Cheminform. 31: no-no. DOI: 10.1002/chin.200001108 |
0.479 |
|
| 2010 |
Yamamoto H, Saito S. ChemInform Abstract: Designer Lewis Acid Catalysts for Selective Organic Synthesis Cheminform. 30: no-no. DOI: 10.1002/CHIN.199952282 |
0.328 |
|
| 2010 |
SAITO S, YAMAMOTO H. ChemInform Abstract: Designer Lewis Acid Catalysts - Bulky Aluminum Reagents for Selective Organic Synthesis Cheminform. 28: no-no. DOI: 10.1002/CHIN.199751292 |
0.346 |
|
| 2010 |
SAITO S, SHIMADA I, TAKAMORI Y, TANAKA M, MARUOKA K, YAMAMOTO H. ChemInform Abstract: Regioselective Robinson Annulation Realized by the Combined Use of Lithium Enolates and Aluminum Tris(2,6-diphenylphenoxide) (ATPH). Cheminform. 28: no-no. DOI: 10.1002/chin.199745051 |
0.412 |
|
| 2010 |
SAITO S, ITO M, MARUOKA K, YAMAMOTO H. ChemInform Abstract: Selective Alkylation of Ketones with a Bulky Aluminum Reagent - The THF-TBSOTf System. Cheminform. 28: no-no. DOI: 10.1002/chin.199742066 |
0.47 |
|
| 2010 |
SAITO S, SHIMADA K, YAMAMOTO H. ChemInform Abstract: Aluminum Tris(4-bromo-2,6-diphenylphenoxide)(ATPH-Br): An Effective Catalyst for Claisen Rearrangement. Cheminform. 27: no-no. DOI: 10.1002/CHIN.199649061 |
0.305 |
|
| 2010 |
MARUOKA K, SAITO S, YAMAMOTO H. ChemInform Abstract: Aluminum Tris(2,6-diphenylphenoxide) (ATPH) as an Extremely Selective Activator of Less Hindered Aldehyde Carbonyls. Cheminform. 26: no-no. DOI: 10.1002/chin.199503040 |
0.423 |
|
| 2010 |
MARUOKA K, AKAKURA M, SAITO S, OOI T, YAMAMOTO H. ChemInform Abstract: Asymmetric Diels-Alder Reaction of Unsymmetrical Maleates. A Chemical Access to Chiral, Unsymmetrical cis-Cyclohexene-1,2-dicarboxylates. Cheminform. 25: no-no. DOI: 10.1002/chin.199451049 |
0.61 |
|
| 2010 |
MARUOKA K, IMOTO H, SAITO S, YAMAMOTO H. ChemInform Abstract: Virtually Complete Blocking of α,β-Unsaturated Aldehyde Carbonyls by Complexation with Aluminum Tris(2,6-diphenylphenoxide). Cheminform. 25: no-no. DOI: 10.1002/chin.199436049 |
0.379 |
|
| 2010 |
MARUOKA K, SHIOHARA K, OISHI M, SAITO S, YAMAMOTO H. ChemInform Abstract: A New Strategy for Obtaining High Level of Diastereoselectivity in the Asymmetric Diels-Alder Reaction of Chiral Dienophiles. Cheminform. 25: no-no. DOI: 10.1002/chin.199405070 |
0.495 |
|
| 2010 |
MARUOKA K, SAITO S, CONCEPCION AB, YAMAMOTO H. ChemInform Abstract: Chemoselective Functionalization of More Hindered Aldehyde Carbonyls with the Methylaluminum Bis(2,6-diphenylphenoxide)/Alkyllithium System. Cheminform. 24: no-no. DOI: 10.1002/chin.199322146 |
0.438 |
|
| 2010 |
MARUOKA K, SAITO S, OOI T, YAMAMOTO H. ChemInform Abstract: Selective Reduction of Methylenecycloalkane Oxides with 4-Substituted Diisobutylaluminum 2,6-Di-tert-butylphenoxides. Cheminform. 23: no-no. DOI: 10.1002/chin.199201108 |
0.545 |
|
| 2009 |
Oishi S, Yoshimoto J, Saito S. Importance of open structure of nonmetal based catalyst in hydrogen bond promoted methanolysis of activated amide: structure dynamics between monomer and dimer enabling recombinant covalent, dative, and hydrogen bonds. Journal of the American Chemical Society. 131: 8748-9. PMID 19496535 DOI: 10.1021/Ja9029494 |
0.3 |
|
| 2009 |
Kracht D, Saito S, Wünsch B. Synthesis of 1,4-Diazabicyclo[3.3.1]nonan-6-ones Australian Journal of Chemistry. 62: 1684. DOI: 10.1071/Ch09206 |
0.384 |
|
| 2009 |
Yoshimoto J, Sandoval CA, Saito S. ChemInform Abstract: Aqua-aminoorganoboron Catalyst: Engineering Single Water Molecule to Act as an Acid Catalyst in Nitro Aldol Reaction. Cheminform. 40. DOI: 10.1002/chin.200920038 |
0.314 |
|
| 2008 |
Tsubogo T, Saito S, Seki K, Yamashita Y, Kobayashi S. Development of catalytic asymmetric 1,4-addition and [3 + 2] cycloaddition reactions using chiral calcium complexes. Journal of the American Chemical Society. 130: 13321-32. PMID 18783222 DOI: 10.1021/ja8032058 |
0.382 |
|
| 2008 |
Goto A, Endo K, Ukai Y, Irle S, Saito S. RhI-catalyzed aldol-type reaction of organonitriles under mild conditions. Chemical Communications (Cambridge, England). 2212-4. PMID 18463743 DOI: 10.1039/B800634B |
0.39 |
|
| 2008 |
Goto A, Endo K, Saito S. Rh(I)-catalyzed hydration of organonitriles under ambient conditions. Angewandte Chemie (International Ed. in English). 47: 3607-9. PMID 18383568 DOI: 10.1002/Anie.200800366 |
0.321 |
|
| 2008 |
Saito S, Momiyama N, Yamamoto H. Development of Organocatalysis Based on the Molecular Design of Pyrrolidine-Brensted Acid Catalysts Journal of Synthetic Organic Chemistry, Japan. 66: 774-784. DOI: 10.5059/Yukigoseikyokaishi.66.774 |
0.57 |
|
| 2008 |
Yoshimoto J, Sandoval CA, Saito S. Aqua-aminoorganoboron catalyst: Engineering single water molecule to act as an acid catalyst in nitro aldol reaction Chemistry Letters. 37: 1294-1295. DOI: 10.1246/Cl.2008.1294 |
0.421 |
|
| 2008 |
Saito S, Momiyama N, Yamamoto H. Development of organocatalysis based on the molecular design of pyrrolidine-Brønsted acid catalysts Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry. 66: 774-784. |
0.628 |
|
| 2007 |
Saito S, Tsubogo T, Kobayashi S. Direct-type catalytic Mannich reactions of amides with imines. Chemical Communications (Cambridge, England). 1236-7. PMID 17356767 DOI: 10.1039/b618490a |
0.366 |
|
| 2006 |
Saito S, Kobayashi S. Highly anti-selective catalytic aldol reactions of amides with aldehydes. Journal of the American Chemical Society. 128: 8704-5. PMID 16819844 DOI: 10.1021/ja061221t |
0.37 |
|
| 2006 |
Kobayashi S, Saito S. Highly anti-Selective Catalytic Aldol Reactions of Amides with Aldehydes Synfacts. 2006: 1038-1038. DOI: 10.1055/s-2006-949342 |
0.318 |
|
| 2004 |
Saito S, Yamamoto H. Design of acid-base catalysis for the asymmetric direct Aldol reaction. Accounts of Chemical Research. 37: 570-9. PMID 15311956 DOI: 10.1021/Ar030064P |
0.549 |
|
| 2004 |
Kobayashi S, Ueno M, Saito S, Mizuki Y, Ishitani H, Yamashita Y. Air-stable, storable, and highly efficient chiral zirconium catalysts for enantioselective Mannich-type, aza Diels-Alder, aldol, and hetero Diels-Alder reactions. Proceedings of the National Academy of Sciences of the United States of America. 101: 5476-81. PMID 15067139 DOI: 10.1073/pnas.0307870101 |
0.382 |
|
| 2004 |
Momiyama N, Torii H, Saito S, Yamamoto H. O-nitroso aldol synthesis: Catalytic enantioselective route to alpha-aminooxy carbonyl compounds via enamine intermediate. Proceedings of the National Academy of Sciences of the United States of America. 101: 5374-8. PMID 15067138 DOI: 10.1073/Pnas.0307785101 |
0.724 |
|
| 2004 |
Torii H, Nakadai M, Ishihara K, Saito S, Yamamoto H. Asymmetric direct aldol reaction assisted by water and a proline-derived tetrazole catalyst. Angewandte Chemie (International Ed. in English). 43: 1983-6. PMID 15065280 DOI: 10.1002/Anie.200352724 |
0.629 |
|
| 2004 |
Ito H, Nagahara T, Ishihara K, Saito S, Yamamoto H. Chiral molecular recognition by aluminum tris(2,6-diphenylphenoxide) in an asymmetric 1,4-addition. Angewandte Chemie (International Ed. in English). 43: 994-7. PMID 14966889 DOI: 10.1002/Anie.200352809 |
0.578 |
|
| 2004 |
Sato A, Hattori A, Ishihara K, Saito S, Yamamoto H. A New Method for the Preparation of Aluminum and Titanium Tris(2,6-diphenylphenoxide) Reagents and Their Application in Organic Synthesis. Cheminform. 35. DOI: 10.1246/Cl.2003.1006 |
0.636 |
|
| 2004 |
Takikawa H, Ishihara K, Saito S, Yamamoto H. Asymmetric vinylogous direct aldol reaction using aluminum tris[2,6-bis(4-alkylphenyl)phenoxide] Synlett. 2004: 732-734. DOI: 10.1055/S-2004-817761 |
0.632 |
|
| 2004 |
Takikawa H, Ishihara K, Saito S, Yamamoto H. Asymmetric Vinylogous Direct Aldol Reaction Using Aluminum Tris[2,6-bis(4-alkylphenyl)phenoxide]. Cheminform. 35. DOI: 10.1002/CHIN.200430033 |
0.517 |
|
| 2003 |
Kobayashi S, Saito S, Ueno M, Yamashita Y. An air-stable, storable chiral zirconium catalyst for asymmetric aldol reactions. Chemical Communications (Cambridge, England). 2016-7. PMID 12934889 DOI: 10.1039/B305273G |
0.387 |
|
| 2003 |
Saito S, Nagahara T, Shiozawa M, Nakadai M, Yamamoto H. Molecular recognition of alpha,beta-unsaturated carbonyl compounds using aluminum tris(2,6-diphenylphenoxide) (ATPH): structural and conformational analysis of ATPH complexes and application to the selective vinylogous aldol reaction. Journal of the American Chemical Society. 125: 6200-10. PMID 12785852 DOI: 10.1021/Ja0205941 |
0.448 |
|
| 2003 |
Yamashita Y, Saito S, Ishitani H, Kobayashi S. Chiral hetero Diels-Alder products by enantioselective and diastereoselective zirconium catalysis. Scope, limitation, mechanism, and application to the concise synthesis of (+)-Prelactone C and (+)-9-deoxygoniopypyrone. Journal of the American Chemical Society. 125: 3793-8. PMID 12656612 DOI: 10.1021/ja028186k |
0.385 |
|
| 2003 |
Sato A, Hattori A, Ishihara K, Saito S, Yamamoto H. A New Method for the Preparation of Aluminum and Titanium Tris(2,6-diphenylphenoxide) Reagents and Their Application in Organic Synthesis Chemistry Letters. 32: 1006-1007. DOI: 10.1246/CL.2003.1006 |
0.466 |
|
| 2003 |
Nakadai M, Saito S, Yamamoto H. Diversity-Based Strategy for Discovery of Environmentally Benign Organocatalyst: Diamine—Protonic Acid Catalysts for Asymmetric Direct Aldol Reaction. Cheminform. 34. DOI: 10.1002/CHIN.200308033 |
0.372 |
|
| 2002 |
Kano T, Ohyabu Y, Saito S, Yamamoto H. Asymmetric carbon-carbon coupling of phenols or anilines with aryllead triacetates. Journal of the American Chemical Society. 124: 5365-73. PMID 11996577 DOI: 10.1021/Ja012287L |
0.617 |
|
| 2002 |
Yamashita Y, Saito S, Ishitani H, Kobayashi S. Catalytic, asymmetric trans-selective hetero Diels-Alder reactions using a chiral zirconium complex. Organic Letters. 4: 1221-3. PMID 11922823 DOI: 10.1021/ol025745j |
0.375 |
|
| 2002 |
Nakadai M, Saito S, Yamamoto H. Diversity-based strategy for discovery of environmentally benign organocatalyst: diamine–protonic acid catalysts for asymmetric direct aldol reaction Tetrahedron. 58: 8167-8177. DOI: 10.1016/S0040-4020(02)00965-1 |
0.491 |
|
| 2001 |
Saito S, Yamazaki S, Yamamoto H. Novel Three-Component Coupling Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): The Same Synthetic Strategy Leads to trans- and cis-Jasmonates. Angewandte Chemie (International Ed. in English). 40: 3613-3617. PMID 11592197 DOI: 10.1002/1521-3773(20011001)40:19<3613::Aid-Anie3613>3.0.Co;2-3 |
0.402 |
|
| 2001 |
Saito S, Hatanaka K, Yamamoto H. Nucleophilic Addition of Organomagnesiums to Aldimines: Scandium Triflate (Sc(OTf)3) as an Effective Catalyst Synlett. 2001: 1859-1861. DOI: 10.1055/S-2001-18755 |
0.412 |
|
| 2001 |
Saito S, Nagahara T, Yamamoto H. Efficient Dehydration of Hydroxyenals and -enones: HfCl4 · (THF)2 as an effective Catalyst for Di-, Tri- and Tetraene Formation Synlett. 2001: 1690-1692. DOI: 10.1055/S-2001-18094 |
0.41 |
|
| 2001 |
Saito S, Nakadai M, Yamamoto H. Diamine-Protonic Acid Catalysts for Catalytic Asymmetric Aldol Reaction Synlett. 2001: 1245-1248. DOI: 10.1055/S-2001-16055 |
0.475 |
|
| 2001 |
Saito S, Hatanaka K, Yamamoto H. Asymmetric Mannich-type reactions with a chiral acetate: effect of Lewis acid on activation of aldimine Tetrahedron. 57: 875-887. DOI: 10.1016/S0040-4020(00)01042-5 |
0.548 |
|
| 2000 |
Saito S, Kano T, Ohyabu Y, Yamamoto H. Direct coupling of anilines with aryllead triacetates Synlett. 1676-1678. DOI: 10.1055/S-2000-7916 |
0.495 |
|
| 2000 |
Saito S, Nakadai M, Yamamoto H. Regio- and Enantioselective Siloxybutylation at the More Hindered α-Site of Unsymmetrical Ketone Using Chiral Aluminum Trisnaphthoxide Synlett. 2000: 1107-1110. DOI: 10.1055/S-2000-6736 |
0.457 |
|
| 2000 |
Saito S, Sone T, Murase M, Yamamoto H. Aluminum Tris(2,6-diphenylphenoxide)-ArCOCl Complex for Nucleophilic Dearomatic Functionalization Journal of the American Chemical Society. 122: 10216-10217. DOI: 10.1021/Ja0014382 |
0.366 |
|
| 2000 |
Saito S, Shiozawa M, Nagahara T, Nakadai M, Yamamoto H. Molecular Recognition of Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): New Regio- and Stereoselective Alkylation of α,β-Unsaturated Carbonyl Compounds Journal of the American Chemical Society. 122: 7847-7848. DOI: 10.1021/Ja000789D |
0.424 |
|
| 2000 |
Saito S, Hatanaka K, Yamamoto H. ChemInform Abstract: Asymmetric Mannich-Type Reactions of Aldimines with a Chiral Acetate. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200042030 |
0.336 |
|
| 1999 |
Saito S, Shiozawa M, Yamamoto H. Mixed Crossed Aldol Condensation between Conjugated Esters and Aldehydes Using Aluminum Tris(2,6-diphenylphenoxide). Angewandte Chemie (International Ed. in English). 38: 1769-1771. PMID 29711211 DOI: 10.1002/(Sici)1521-3773(19990614)38:12<1769::Aid-Anie1769>3.0.Co;2-0 |
0.443 |
|
| 1999 |
Yamamoto H, Saito S. Designer Lewis acid catalysts for selective organic synthesis Pure and Applied Chemistry. 71: 239-245. DOI: 10.1351/Pac199971020239 |
0.53 |
|
| 1999 |
Saito S, Yamazaki S, Shiozawa M, Yamamoto H. Novel Three Component Coupling of Ketone, Cyclic Ether and Epoxide using Aluminum Tris(2,6-diphenylphenoxide) (ATPH) Synlett. 1999: 581-583. DOI: 10.1055/S-1999-2657 |
0.363 |
|
| 1999 |
Saito S. Conjugate Addition of Lithium Enolates to Aromatic Carbonyl Compounds Complexed with Aluminum Tris(2,6-diphenylphenoxide) (ATPH) Synlett. 1999: 81-83. DOI: 10.1055/S-1999-2527 |
0.313 |
|
| 1999 |
Saito S. Aluminum Trisphenoxide Polymer as a Lewis Acidic, Solid Catalyst Synlett. 1999: 57-58. DOI: 10.1055/S-1999-2523 |
0.361 |
|
| 1999 |
Saito S, Kano T, Muto H, Nakadai M, Yamamoto H. Asymmetric coupling of phenols with arylleads [2] Journal of the American Chemical Society. 121: 8943-8944. DOI: 10.1021/Ja990646V |
0.567 |
|
| 1999 |
Saito S, Hatanaka K, Kano T, Yamamoto H. Diastereoselective aldol reaction with an acetate enolate: 2,6-Bis(2- isopropylphenyl)-3,5-dimethylphenol as an extremely effective chiral auxiliary Angewandte Chemie - International Edition. 37: 3378-3381. DOI: 10.1002/(SICI)1521-3773(19981231)37:24<3378::AID-ANIE3378>3.0.CO;2-L |
0.627 |
|
| 1999 |
Saito S, Yamamoto H. Directed Aldol Condensation Chemistry - a European Journal. 5: 1959-1962. DOI: 10.1002/(Sici)1521-3765(19990702)5:7<1959::Aid-Chem1959>3.0.Co;2-7 |
0.425 |
|
| 1999 |
Saito S, Shiozawa M, Yamamoto H. Gemischte Aldol-Kreuzkondensation zwischen konjugierten Estern und Aldehyden mit Aluminiumtris(2,6-diphenylphenoxid) Angewandte Chemie. 111: 1884-1886. DOI: 10.1002/(Sici)1521-3757(19990614)111:12<1884::Aid-Ange1884>3.0.Co;2-2 |
0.429 |
|
| 1998 |
Saito S, Hatanaka K, Kano T, Yamamoto H. Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary. Angewandte Chemie (International Ed. in English). 37: 3378-3381. PMID 29711286 DOI: 10.1002/(Sici)1521-3773(19981231)37:24<3378::Aid-Anie3378>3.0.Co;2-L |
0.665 |
|
| 1998 |
Yamamoto H, Yanagisawa A, Ishihara K, Saito S. Designer Lewis acids for selective organic synthesis Pure and Applied Chemistry. 70. DOI: 10.5059/Yukigoseikyokaishi.52.912 |
0.629 |
|
| 1998 |
Saito S, Shiozawa M, Ito M, Yamamoto H. Conceptually New Directed Aldol Condensation Using Aluminum Tris(2,6-diphenylphenoxide) Journal of the American Chemical Society. 120: 813-814. DOI: 10.1021/Ja972765L |
0.428 |
|
| 1998 |
Saito S, Hatanaka K, Kano T, Yamamoto H. Diastereoselektive Aldolreaktion mit einem Acetat-Enolat: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol als äußerst effektives chirales Auxiliar Angewandte Chemie. 110: 3579-3582. DOI: 10.1002/(Sici)1521-3757(19981217)110:24<3579::Aid-Ange3579>3.0.Co;2-S |
0.558 |
|
| 1997 |
Saito S, Shimada I, Takamori Y, Tanaka M, Maruoka K, Yamamoto H. Regioselective Robinson Annulation Realized by the Combined Use of Lithium Enolates and Aluminum Tris(2,6-diphenylphenoxide) (ATPH) Bulletin of the Chemical Society of Japan. 70: 1671-1681. DOI: 10.1246/Bcsj.70.1671 |
0.581 |
|
| 1997 |
Saito S, Shiozawa M, Takamori Y, Yamamoto H. A New Annulation Based on a One-Pot Double Michael Addition Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH) Synlett. 1997: 359-360. DOI: 10.1055/S-1997-793 |
0.35 |
|
| 1997 |
Saito S, Ito M, Maruoka K, Yamamoto H. Selective Alkylation of Ketones with a Bulky Aluminum Reagent-the THF-TBSOTf System Synlett. 1997: 357-358. DOI: 10.1055/S-1997-792 |
0.581 |
|
| 1997 |
Saito S, Shimada K, Yamamoto H, Marigorta EMd, Fleming I. A new synthetic route to allylsilanes: the reaction of silyllithium reagents with aromatic carbonyl compounds and aluminium tris(2,6-diphenylphenoxide) (ATPH) Chemical Communications. 1299-1300. DOI: 10.1039/A702684F |
0.518 |
|
| 1997 |
Saito S, Yamamoto H. Designer Lewis Acid Catalysts-Bulky Aluminium Reagents For Selective Organic Synthesis Chemical Communications. 1585-1592. DOI: 10.1039/A607464B |
0.57 |
|
| 1997 |
Saito S, Kano T, Hatanaka K, Yamamoto H. 2,6-Bis(2-alkylphenyl)-3,5-dimethylphenol as a new chiral phenol with C2-symmetry. Application to the asymmetric alkylation of aldehydes Journal of Organic Chemistry. 62: 5651-5656. DOI: 10.1021/Jo970747G |
0.617 |
|
| 1997 |
Saito S, Ito M, Yamamoto H. Highly Regioselective Alkylation at the More-Hindered α-Site of Unsymmetrical Ketones by the Combined Use of Aluminum Tris(2,6-diphenylphenoxide) and Lithium Diisopropylamide Journal of the American Chemical Society. 119: 611-612. DOI: 10.1021/Ja963274O |
0.34 |
|
| 1996 |
Saito S, Yamamoto H. Efficient Conjugate Reduction of alpha,beta-Unsaturated Carbonyl Compounds by Complexation with Aluminum Tris(2,6-diphenylphenoxide). The Journal of Organic Chemistry. 61: 2928-2929. PMID 11667146 DOI: 10.1021/Jo960161E |
0.383 |
|
| 1996 |
Saito S, Shimada K, Yamamoto H. Aluminum Tris(4-bromo-2,6-diphenylphenoxide) (ATPH-Br): an Effective Catalyst for Claisen Rearrangement Synlett. 1996: 720-722. DOI: 10.1055/S-1996-5517 |
0.491 |
|
| 1995 |
Maruoka K, Saito S, Yamamoto H. Molecular Design of a Chiral Lewis Acid for the Asymmetric Claisen Rearrangement Journal of the American Chemical Society. 117: 1165-1166. DOI: 10.1021/Ja00108A048 |
0.565 |
|
| 1994 |
Maruoka K, Saito S, Yamamoto H. Aluminum Tris(2,6-diphenylphenoxide) (ATPH) as an Extremely Selective Activator of Less Hindered Aldehyde Carbonyls Synlett. 1994: 439-440. DOI: 10.1055/S-1994-22881 |
0.48 |
|
| 1994 |
Maruoka K, Akakura M, Saito S, Ooi T, Yamamoto H. Asymmetric Diels-Alder Reaction of Unsymmetrical Maleates. A Chemical Access to Chiral, Unsymmetrical cis-Cyclohexene-1,2-dicarboxylates Journal of the American Chemical Society. 116: 6153-6158. DOI: 10.1021/Ja00093A013 |
0.638 |
|
| 1994 |
Maruoka K, Imoto H, Saito S, Yamamoto H. Virtually Complete Blocking of .alpha.,.beta.-Unsaturated Aldehyde Carbonyls by Complexation with Aluminum Tris(2,6-diphenylphenoxide) Journal of the American Chemical Society. 116: 4131-4132. DOI: 10.1021/Ja00088A080 |
0.482 |
|
| 1993 |
Maruoka K, Shiohara K, Oishi M, Saito S, Yamamoto H. A New Strategy for Obtaining High Level of Diastereoselectivity in the Asymmetric Diels-Alder Reaction of Chiral Dienophiles Synlett. 1993: 421-422. DOI: 10.1055/S-1993-22479 |
0.55 |
|
| 1993 |
Maruoka K, Imoto H, Saito S, Yamamoto H. Regiocontrolled [2+2] Cycloaddition of Unsymmetrical Fumarates Based on the Discrimination of Two Different Ester Carbonyls with Methylaluminum Bis(2,6-di-tert-butyl-4-methylphenoxide) (MAD) Synlett. 1993: 197-198. DOI: 10.1055/S-1993-22399 |
0.519 |
|
| 1993 |
Maruoka K, Saito S, Concepcion AB, Yamamoto H. Chemoselective functionalization of more hindered aldehyde carbonyls with the methylaluminum bis(2,6-diphenylphenoxide)/alkyllithium system Journal of the American Chemical Society. 115: 1183-1184. DOI: 10.1021/Ja00056A073 |
0.495 |
|
| 1992 |
Maruoka K, Saito S, Yamamoto H. Discrimination of two different ester carbonyls with methylaluminum bis(2,6-di-tert-butyl-4-methylphenoxide). Application to the regiocontrolled and stereocontrolled Diels-Alder reaction of unsymmetrical fumarates Journal of the American Chemical Society. 114: 1089-1090. DOI: 10.1021/Ja00029A048 |
0.537 |
|
| 1991 |
Maruoka K, Saito S, Ooi T, Yamamoto H. A New Stereoselective Approach to Oxygenated Carbocycles: Asymmetric Synthesis of the Cyclohexyl Fragment of FK-506 Synlett. 1991: 579-580. DOI: 10.1055/S-1991-21983 |
0.635 |
|
| 1991 |
Maruoka K, Saito S, Ooi T, Yamamoto H. Selective Reduction of Methylenecycloalkane Oxides with 4-Substituted Diisobutylaluminum 2,6-Di-tert-butylphenoxides Synlett. 1991: 255-256. DOI: 10.1055/S-1991-20698 |
0.575 |
|
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