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Pure Appl. Chem., 1992, Vol. 64, No. 3, pp. 315-322

http://dx.doi.org/10.1351/pac199264030315

Abiological catalysis for synthetic efficiency

B. M. Trost

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  • Gumrukcu Yasemin, de Bruin Bas, Reek Joost N. H.: Hydrogen-Bond-Assisted Activation of Allylic Alcohols for Palladium-Catalyzed Coupling Reactions. ChemSusChem 2014, 7, 890. <http://dx.doi.org/10.1002/cssc.201300723>
  • Sharma Manu, Das Debashree, Baruah Arabinda, Jain Archana, Ganguli Ashok K.: Design of Porous Silica Supported Tantalum Oxide Hollow Spheres Showing Enhanced Photocatalytic Activity. Langmuir 2014, 30, 3199. <http://dx.doi.org/10.1021/la500167a>
  • Gu Xin, Wang Xiaoyan, Wang Fengtian, Sun Hongbao, Liu Jie, Xie Yongmei, Xiang Mingli: Pyrrolidine-Mediated Direct Preparation of (E)-Monoarylidene Derivatives of Homo- and Heterocyclic Ketones with Various Aldehydes. Molecules 2014, 19, 1976. <http://dx.doi.org/10.3390/molecules19021976>
  • Zhang Jingjing, Niu Youhong, Cao Xiaoping, Ye Xin-Shan: Convenient one-pot synthesis of thiosugars and their efficient conversion to polyoxygenated cycloalkenes. Tetrahedron 2012, 68, 4242. <http://dx.doi.org/10.1016/j.tet.2012.03.086>
  • TROST B. M.: ChemInform Abstract: Abiological Catalysis for Synthetic Efficiency. ChemInform 2010, 23, no. <http://dx.doi.org/10.1002/chin.199232276>
  • Grandbois Alain, Mayer Marie-Ève, Bédard Marion, Collins Shawn K., Michel Typhène: Synthesis of C 1-Symmetric BINOLs Employing N-Heterocyclic Carbene-Copper Complexes. Chem Eur J 2009, 15, 9655. <http://dx.doi.org/10.1002/chem.200901295>
  • Gan Kim-Hong, Jhong Ciou-Jyu, Yang Shyh-Chyun: Direct palladium/carboxylic acid-catalyzed C-allylation of cyclic 1,3-diones with allylic alcohols in water. Tetrahedron 2008, 64, 1204. <http://dx.doi.org/10.1016/j.tet.2007.11.082>
  • Gan Kim-Hong, Jhong Ciou-Jyu, Shue Yi-Jen, Yang Shyh-Chyun: Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates in water. Tetrahedron 2008, 64, 9625. <http://dx.doi.org/10.1016/j.tet.2008.07.037>
  • Lee Sang Ick, Park Se Yeoun, Chung Young Keun: Rhodium-Catalyzed [4+2+2] Cycloaddition Reaction of Two Enynes or Diynes with One Diene to Give Eight-Membered Ring Compounds. Adv Synth Catal 2006, 348, 2531. <http://dx.doi.org/10.1002/adsc.200600321>
  • Yang Shyh-Chyun, Feng Wei-Hao, Gan Kim-Hong: Platinum-catalyzed allylation of aminonaphthalenes with allylic acetates. Tetrahedron 2006, 62, 3752. <http://dx.doi.org/10.1016/j.tet.2006.01.023>
  • Yang Shyh-Chyun, Hsu Yi-Chun, Gan Kim-Hong: Direct palladium/carboxylic acid-catalyzed allylation of anilines with allylic alcohols in water. Tetrahedron 2006, 62, 3949. <http://dx.doi.org/10.1016/j.tet.2006.02.035>
  • Ikeda Takahiro, Misawa Naohisa, Ichihashi Yuichi, Nishiyama Satoru, Tsuruya Shigeru: Liquid-phase oxidative coupling of 2-naphthol by vanadium catalysts supported on MCM-41. Journal of Molecular Catalysis A 2005, 231, 235. <http://dx.doi.org/10.1016/j.molcata.2005.01.012>
  • Yamamoto Yoshihiko, Ishii Jun-ichi, Nishiyama Hisao, Itoh Kenji: One-pot sequential four-component coupling via Cp*RuCl-catalyzed cyclotrimerization and Suzuki–Miyaura coupling. Tetrahedron 2005, 61, 11501. <http://dx.doi.org/10.1016/j.tet.2005.08.069>
  • Hsu Yi-Chun, Gan Kim-Hong, Yang Shyh-Chyun: Palladium-Catalyzed Allylation of Acidic and Less Nucleophilic Anilines Using Allylic Alcohols Directly. Chem Pharm Bull 2005, 53, 1266. <http://dx.doi.org/10.1248/cpb.53.1266>
  • Yang Shyh-Chyun, Lai Hwe-Chen, Tsai Yan-Chiu: Palladium-catalyzed regiospecific tandem allylation of 2-aminophenols using 2-butene-1,4-diol. Tetrahetron Lett 2004, 45, 2693. <http://dx.doi.org/10.1016/j.tetlet.2004.01.128>
  • Yang Shyh-Chyun, Liu Pei-Chin, Feng Wei-Hao: Palladium-catalyzed tandem allylation of 1,2-phenylenediamines with cis-1,4-diacetoxy-2-butene. Tetrahetron Lett 2004, 45, 4951. <http://dx.doi.org/10.1016/j.tetlet.2004.04.140>
  • Kimura Masanari, Mukai Ryutaro, Tanigawa Naoko, Tanaka Shuji, Tamaru Yoshinao: Triethylborane as an efficient promoter for palladium-catalyzed allylation of active methylene compounds with allyl alcohols. Tetrahedron 2003, 59, 7767. <http://dx.doi.org/10.1016/S0040-4020(03)01234-1>
  • Shue Yi-Jen, Yang Shyh-Chyun, Lai Hwe-Chen: Direct palladium(0)-catalyzed amination of allylic alcohols with aminonaphthalenes. Tetrahetron Lett 2003, 44, 1481. <http://dx.doi.org/10.1016/S0040-4039(02)02861-7>
  • Kreher Ulf P., Rosamilia Anthony E., Raston Colin L., Scott Janet L., Strauss Christopher R.: Direct Preparation of Monoarylidene Derivatives of Aldehydes and Enolizable Ketones with DIMCARB. Org Lett 2003, 5, 3107. <http://dx.doi.org/10.1021/ol0351145>
  • Ji Shun-Jun, Lu Jianmei, Zhu Xinlin, Yang Jin, Lang Jian-Ping, Wu Lin: MICROWAVE-ASSISTED EFFICIENT OXIDATIVE COUPLING OF 2-NAPHTHOLS IN THE SOLID STATE. Synth Common 2002, 32, 3069. <http://dx.doi.org/10.1081/SCC-120013000>
  • Horino Yoshikazu, Naito Makoto, Kimura Masanari, Tanaka Shuji, Tamaru Yoshinao: Et3B-promoted, Pd-catalyzed C-allylation of o-hydroxyacetophenone and its derivatives with allyl alcohols. Tetrahetron Lett 2001, 42, 3113. <http://dx.doi.org/10.1016/S0040-4039(01)00381-1>
  • Mastrorilli P., Muscio F., Suranna G.P., Nobile C.F., Latronico M.: Aerobic oxidation of substituted phenols catalysed by metal acetylacetonates in the presence of 3-methylbutanal. Journal of Molecular Catalysis A 2001, 165, 81. <http://dx.doi.org/10.1016/S1381-1169(00)00437-4>
  • König Burkhard: Homogene Metallkatalyse - effektiv, aber auch effizient?. Chem Unserer Zeit 1998, 32, 136. <http://dx.doi.org/10.1002/ciuz.19980320304>
  • Muchow Gunter, Brunel Jean Michel, Maffei Michel, Pardigon Olivier, Buono Gérard: Pd(0) catalyzed asymmetric amination of a prochiral bicyclic allylic diacetate. Tetrahedron 1998, 54, 10435. <http://dx.doi.org/10.1016/S0040-4020(98)00496-7>
  • Kumareswaran R., Vankar Yashwant D.: Palladium catalysed allylic substitution via in situ activation of allylic alcohols. Tetrahetron Lett 1997, 38, 8421. <http://dx.doi.org/10.1016/S0040-4039(97)10237-4>
  • Bräse Stefan, Schömenauer Sten, McGaffin Gregory, Stolle Andreas, de Meijere Armin: Versatile Synthesis of Enantiomerically Pure 2-Alkoxy-1-Ethynylcyclopropanes and their Application in the Synthesis of Enantiomerically Pure Bicyclo-[3.3.0]oct-1-en-3-ones. Chem Eur J 1996, 2, 545. <http://dx.doi.org/10.1002/chem.19960020514>
  • Zhu Guoxin, Lu Xiyan: Molecular oxygen promoted oxidative cleavage of carbon-palladium bonds — catalytic cyclization of allylic 2-alkynoates to α-alkylidine-γ-butyrolactones by a PdII complex. J Organomet Chem 1996, 508, 83. <http://dx.doi.org/10.1016/0022-328X(95)05781-J>
  • Ding Kuiling, Yang Wang, Zhang Lijun, Yangjie Wu, Matsuura Teruo: A novel two-phase oxidative coupling of 2-naphthols suspended in aqueous Fe3+ solutions. Tetrahedron 1996, 52, 1005. <http://dx.doi.org/10.1016/0040-4020(95)00941-8>
  • Jiang Huanfeng, Ma Shengming, Zhu Guoxin, Lu Xiyan: Structural factors affecting the selectivities in the palladium (II) catalyzed cyclization of N-alkenyl-2-alkynamides. Tetrahedron 1996, 52, 10945. <http://dx.doi.org/10.1016/0040-4020(96)00648-5>
  • Holý Petr, Bělohradský Martin, Závada Jiří: A Novel One-Pot Conversion of 2-Naphthols into 1,1′-Binaphthalene-2,2′-Diols. Synth Common 1996, 26, 2597. <http://dx.doi.org/10.1080/00397919608004572>
  • Starý Ivo, Stará Irena G., Kocˇovský Pavel: Palladium(O)-catalyzed allylic substitution with allylic alkoxides as substrates. Tetrahedron 1994, 50, 529. <http://dx.doi.org/10.1016/S0040-4020(01)80774-2>
  • Bajgrowicz Jerzy A., Petrzilka Martin: 3,3-dimethyl-7-methylenecycloocta-1,5-dione, a versatile building block for the preparation of substituted cyclooctadienones and δ-valerolactones. Tetrahedron 1994, 50, 7461. <http://dx.doi.org/10.1016/S0040-4020(01)90474-0>
  • Starý Ivo, Stará Irena G., Kočovský Pavel: Allylic alcohols as substrates for the palladium(0)-catalyzed allylic substitution. Tetrahetron Lett 1993, 34, 179. <http://dx.doi.org/10.1016/S0040-4039(00)60088-6>
  • Starý Ivo, Zajíček Jaroslav, Kočovský Pavel: Stereochemistry of the palladium-catalyzed allylic substitution: the syn-anti dichotomy in the formation of (π-allyl)palladium complexes and their equilibration. Tetrahedron 1992, 48, 7229. <http://dx.doi.org/10.1016/S0040-4020(01)88263-6>