Pure and Applied Chemistry

CrossRef Cited-by Linking

• Arai Noriyoshi, Sato Keisuke, Azuma Keita, Ohkuma Takeshi: Enantioselective Isomerization of Primary Allylic Alcohols into Chiral Aldehydes with the tol-binap/dbapen/Ruthenium(II) Catalyst. Angew. Chem. 2013, 125, 7648. <http://dx.doi.org/10.1002/ange.201303423>
• Arai Noriyoshi, Sato Keisuke, Azuma Keita, Ohkuma Takeshi: Enantioselective Isomerization of Primary Allylic Alcohols into Chiral Aldehydes with the tol-binap/dbapen/Ruthenium(II) Catalyst. Angew. Chem. Int. Ed. 2013, 52, 7500. <http://dx.doi.org/10.1002/anie.201303423>
• Lin Luqing, Yamamoto Kumiko, Matsunaga Shigeki, Kanai Motomu: Rh-Catalyzed AldehydeAldehyde Cross-Aldol Reaction under Base-Free Conditions: In Situ Aldehyde-Derived Enolate Formation through Orthogonal Activation. Chem. Asian J. 2013, 8, 2974. <http://dx.doi.org/10.1002/asia.201300928>
• Ren Kai, Zhang Lei, Hu Bei, Zhao Mengmeng, Tu Yahui, Xie Xiaomin, Zhang Tony Y., Zhang Zhaoguo: Cationic-Rhodium-Catalyzed Kinetic Resolution of Allylic Alcohols through a Redox Isomerization Reaction in a Noncoordinating Solvent. ChemCatChem 2013, 5, 1317. <http://dx.doi.org/10.1002/cctc.201300014>
• Tasic Gordana, Simic Milena, Popovic Stanimir, Husinec Suren, Maslak Veselin, Savic Vladimir: Indirect N-vinylation of indoles via isomerisation of N-allyl derivatives: synthesis of (±)-debromoarborescidine B. Tetrahedron Letters 2013, 54, 4536. <http://dx.doi.org/10.1016/j.tetlet.2013.06.069>
• Johnston Adam J. S., McLaughlin Mark G., Reid Jolene P., Cook Matthew J.: NaH mediated isomerisation–allylation reaction of 1,3-substituted propenols. Org. Biomol. Chem. 2013, 11, 7662. <http://dx.doi.org/10.1039/c3ob41857j>
• Lin Luqing, Yamamoto Kumiko, Matsunaga Shigeki, Kanai Motomu: Rhodium-Catalyzed Cross-Aldol Reaction: In Situ Aldehyde-Enolate Formation from Allyloxyboranes and Primary Allylic Alcohols. Angew. Chem. 2012, 124, 10421. <http://dx.doi.org/10.1002/ange.201205680>
• Lin Luqing, Yamamoto Kumiko, Matsunaga Shigeki, Kanai Motomu: Rhodium-Catalyzed Cross-Aldol Reaction: In Situ Aldehyde-Enolate Formation from Allyloxyboranes and Primary Allylic Alcohols. Angew. Chem. Int. Ed. 2012, 51, 10275. <http://dx.doi.org/10.1002/anie.201205680>
• Lorenzo-Luis Pablo, Romerosa Antonio, Serrano-Ruiz Manuel: Catalytic Isomerization of Allylic Alcohols in Water. ACS Catal. 2012, 1079. <http://dx.doi.org/10.1021/cs300092d>
• Ahlsten Nanna, Bartoszewicz Agnieszka, Martín-Matute Belén: Allylic alcohols as synthetic enolate equivalents: Isomerisation and tandem reactions catalysed by transition metal complexes. DALTON T 2012, 41, 1660. <http://dx.doi.org/10.1039/c1dt11678a>
• Mantilli Luca, Gérard David, Torche Sonya, Besnard Céline, Mazet Clément: Improved Catalysts for the Iridium-Catalyzed Asymmetric Isomerization of Primary Allylic Alcohols Based on Charton Analysis. Chem Eur J 2010, 16, 12736. <http://dx.doi.org/10.1002/chem.201001311>
• Elferink V. H. M., Breitgoff D., Kloosterman M., Kamphuis J., van den Tweel W. J. J., Meijer E. M.: Industrial developments in biocatalysis. Recl Trav Chim Pays-Bas 2010, 110, 63. <http://dx.doi.org/10.1002/recl.19911100302>
• Fernández-Zúmel Mariano A., Lastra-Barreira Beatriz, Scheele Marcus, Díez Josefina, Crochet Pascale, Gimeno José: Chiral phosphonite, phosphite and phosphoramidite η6-arene-ruthenium(ii) complexes: application to the kinetic resolution of allylic alcohols. Dalton Trans 2010, 39, 7780. <http://dx.doi.org/10.1039/c0dt00140f>
• Mantilli Luca, Gérard David, Torche Sonya, Besnard Céline, Mazet Clément: Iridium-Catalyzed Asymmetric Isomerization of Primary Allylic Alcohols. Angew Chem 2009, 121, 5245. <http://dx.doi.org/10.1002/ange.200901863>
• Mantilli Luca, Gérard David, Torche Sonya, Besnard Céline, Mazet Clément: Iridium-Catalyzed Asymmetric Isomerization of Primary Allylic Alcohols. Angew Chem Int Ed 2009, 48, 5143. <http://dx.doi.org/10.1002/anie.200901863>
• Tanaka Ken, Shoji Takeaki, Hirano Masao: Cationic Rhodium(I)/Bisphosphane Complex-Catalyzed Isomerization of Secondary Propargylic Alcohols to α,β-Enones. Eur J Org Chem 2007, 2007, 2687. <http://dx.doi.org/10.1002/ejoc.200700071>
• Shagufta, Srivastava Ajay Kumar, Panda Gautam: Isomerization of allylic alcohols into saturated carbonyls using phosphorus tribromide. Tetrahetron Lett 2006, 47, 1065. <http://dx.doi.org/10.1016/j.tetlet.2005.12.046>
• Spino Claude: CHIRAL ENOLATE EQUIVALENTS. A REVIEW. Org Prep Proced Int 2003, 35, 1. <http://dx.doi.org/10.1080/00304940309355794>
• Weber Lothar: Phosphorheterocyclen: von Laborkuriositäten zu Liganden in hocheffizienten Katalysatoren. Angew Chem 2002, 114, 583. <http://dx.doi.org/10.1002/1521-3757(20020215)114:4<583::AID-ANGE583>3.0.CO;2-2>
• Weber Lothar: Phosphorus Heterocycles: From Laboratory Curiosities to Ligands in Highly Efficient Catalysts. Angew Chem Int Ed 2002, 41, 563. <http://dx.doi.org/10.1002/1521-3773(20020215)41:4<563::AID-ANIE563>3.0.CO;2-Q>
• van der Drift Robert C., Bouwman Elisabeth, Drent Eite: Homogeneously catalysed isomerisation of allylic alcohols to carbonyl compounds. J Organomet Chem 2002, 650, 1. <http://dx.doi.org/10.1016/S0022-328X(02)01150-6>
• Ershova Victoria A, Golovin Anatoly V, Pogrebnyak Vladimir M: Catalytic isomerization of N-allylic substrates with chiral Os3 clusters as potentially enantioselective reaction. J Organomet Chem 2002, 658, 147. <http://dx.doi.org/10.1016/S0022-328X(02)01643-1>
• Chapuis Christian, Jacoby Denis: Catalysis in the preparation of fragrances and flavours. CATAL A GENERAL 2001, 221, 93. <http://dx.doi.org/10.1016/S0926-860X(01)00798-0>
• Basavaiah Deevi, Muthukumaran Kannan: RuCl₂(PPh₃)₃ Catalyzed Isomerization of the Baylis-Hillman Adducts. Synth Common 1999, 29, 713. <http://dx.doi.org/10.1080/00397919908085821>
• Selective Isomerization of 2-Allylphenol to (Z)-2-Propenylphenol Catalyzed by Ru(cod)(cot)/PEt3. Chem Lett 1999, 441. <http://dx.doi.org/10.1246/cl.1999.441>
• Wang Dong, Chen Dongli, Haberman John X., Li Chao-Jun: Ruthenium-catalyzed isomerization of homoallylic alcohols in water. Tetrahedron 1998, 54, 5129. <http://dx.doi.org/10.1016/S0040-4020(98)00252-X>
• Akutagawa Susumu: Asymmetric synthesis by metal BINAP catalysts. CATAL A GENERAL 1995, 128, 171. <http://dx.doi.org/10.1016/0926-860X(95)00097-6>
• Ammann Christian J., Pregosin Paul S., Rüegger Heinz, Albinati Alberto, Lianza Francesca, Kunz Roland W.: Chemistry of PdII complexes containing both BINAP (2′2′-bis(diphenylphosphino)binaphthyl) and a η3-pinene or -allyl ligand. NMR studies on [Pd(η3-C10H15){S(−)BINAP}] (CF3SO3). The crystal structure of [Pd(η3-C10H15)(4,4′-dimethylbipyridine)](CF3SO3). J Organomet Chem 1992, 423, 415. <http://dx.doi.org/10.1016/0022-328X(92)83135-5>
• Knierzinger Andreas, Walther Willy, Weber Beat, Müller Robert Karl, Netscher Thomas: Eine neue Methode zur stereochemischen Analyse offenkettiger terpenoider Carbonyl-Verbindungen,. HCA 1990, 73, 1087. <http://dx.doi.org/10.1002/hlca.19900730432>
• Hegedus Louis S.: Transition metals in organic synthesis annual survey covering the year 1986. J Organomet Chem 1988, 343, 147. <http://dx.doi.org/10.1016/0022-328X(88)80176-1>
• Consiglio Giambattista, Morandini Franco: Optically active [(η-C5H5)Ru{(R)-Ph2PCH(CH3)CH2PPh2}(Olefin)]PF6 complexes: Influence of the stereogenic metal atom on the enantioface selection. J Organomet Chem 1986, 310, C66. <http://dx.doi.org/10.1016/0022-328X(86)80205-4>