Pure and Applied Chemistry

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• Xu Da-Zhen, Zhan Ming-Zhe, Huang You: A simple and highly efficient procedure for construction of quaternary carbons centers by tributylphosphine catalyzed bis-Michael addition. Tetrahedron 2014, 70, 176. <http://dx.doi.org/10.1016/j.tet.2013.11.103>
• Himmelbauer Martin, Farcet Jean-Baptiste, Gagnepain Julien, Mulzer Johann: An Approach to the Carbon Backbone of Bielschowskysin, Part 1: Photocyclization Strategy. Eur. J. Org. Chem. 2013, 2013, 8214. <http://dx.doi.org/10.1002/ejoc.201300869>
• Nguyen Khanh Hung, Tomasi Sophie, Le Roch Myriam, Toupet Loïc, Renault Jacques, Uriac Philippe, Gouault Nicolas: Gold-Mediated Synthesis and Functionalization of Chiral Halopyridones. J. Org. Chem. 2013, 78, 7809. <http://dx.doi.org/10.1021/jo400827b>
• Himmelbauer Martin, Farcet Jean-Baptiste, Gagnepain Julien, Mulzer Johann: A Palladium-Catalyzed Carbo-oxygenation: The Bielschowskysin Case. Org. Lett. 2013, 15, 3098. <http://dx.doi.org/10.1021/ol401285d>
• Obase Akiko, Kageyama Akihito, Manabe Yuki, Ozawa Tsukasa, Araki Takaaki, Yokoe Hiromasa, Kanematsu Makoto, Yoshida Masahiro, Shishido Kozo: Enantioselective Total Syntheses of Pygmaeocins B and C. Org. Lett. 2013, 15, 3666. <http://dx.doi.org/10.1021/ol401543b>
• Peng Ruogu, VanNieuwenhze Michael S.: A Model Study for Constructing the DEF-Benzoxocin Ring System of Menogaril and Nogalamycin via a Reductive Heck Cyclization. Z Org Lett 2012, 14, 1962. <http://dx.doi.org/10.1021/ol300072h>
• Klein Johannes E. M. N., Taylor Richard J. K.: Transition-Metal-Mediated Routes to 3,3-Disubstituted Oxindoles through Anilide Cyclisation. Eur J Org 2011, 2011, 6821. <http://dx.doi.org/10.1002/ejoc.201100836>
• Aumann Kylee M., Healy Peter C., Coster Mark J.: Arylation of [6,6]-spiroacetal enol ethers: reactivity and rearrangement. Tet Letts 2011, 52, 1070. <http://dx.doi.org/10.1016/j.tetlet.2010.12.076>
• Zhang Ping, Le Hai, Kyne Robert E., Morken James P.: Enantioselective Construction of All-Carbon Quaternary Centers by Branch-Selective Pd-Catalyzed Allyl–Allyl Cross-Coupling. J Am Chem Soc 2011, 133, 9716. <http://dx.doi.org/10.1021/ja2039248>
• Trost Barry M., O'Boyle Brendan M., Hund Daniel: Investigation of a Domino Heck Reaction for the Rapid Synthesis of Bicyclic Natural Products. Chem Eur J 2010, 16, 9772. <http://dx.doi.org/10.1002/chem.201001689>
• OVERMAN L. E.: ChemInform Abstract: Application of Intramolecular Heck Reactions for Forming Congested Quaternary Carbon Centers in Complex Molecule Total Synthesis. ChemInform 2010, 25, no. <http://dx.doi.org/10.1002/chin.199441287>
• Buckley Benjamin R., Neary Stephen P.: Thiadiazolidine 1-oxide systems for phosphine-free palladium-mediated catalysis. Tetrahedron 2010, 66, 7988. <http://dx.doi.org/10.1016/j.tet.2010.08.018>
• Guerrab Zineb, Schweiger Stefan, Daou Boujemâa, Ahmar Mohammed, Cazes Bernard: Lipase-catalyzed kinetic resolution of α-hydroxymethylcycloalkanones with a quaternary carbon center. Chemoenzymatic synthesis of chiral pseudoiridolactones. Tet Asymm 2010, 21, 1752. <http://dx.doi.org/10.1016/j.tetasy.2010.04.043>
• Chapman Lauren M., Adams Bruce, Kliman Laura T., Makriyannis Alexandros, Hamblett Christopher L.: Intramolecular Heck reactions of aryl chlorides with alkynes. Tetrahetron Lett 2010, 51, 1517. <http://dx.doi.org/10.1016/j.tetlet.2010.01.050>
• Saiyed Akeel S., Bedekar Ashutosh V.: One-pot synthesis of stilbenes by dehydrohalogenation–Heck olefination and multicomponent Wittig–Heck reaction. Tetrahetron Lett 2010, 51, 6227. <http://dx.doi.org/10.1016/j.tetlet.2010.09.050>
• Buckley Benjamin R., Neary Stephen P.: The First Thiadiazolidine 1-Oxide System for Phosphine-Free Palladium-Mediated Catalysis. Adv Synth Catal 2009, 351, 71. <http://dx.doi.org/10.1002/adsc.200800522>
• Selig Philipp, Herdtweck Eberhardt, Bach Thorsten: Total Synthesis of Meloscine by a [2+2]-Photocycloaddition/Ring-Expansion Route. Chem Eur J 2009, 15, 3509. <http://dx.doi.org/10.1002/chem.200802383>
• Murakami Yuri, Yoshida Masahiro, Shishido Kozo: Diastereoselective construction of chiral building blocks for the synthesis of indole alkaloids using an intramolecular Heck reaction. Tetrahetron Lett 2009, 50, 1279. <http://dx.doi.org/10.1016/j.tetlet.2008.12.105>
• Kulkarni Mukund G., Dhondge Attrimuni P., Borhade Ajit S., Gaikwad Dnyaneshwar D., Chavhan Sanjay W., Shaikh Yunnus B., Ningdale Vijay B., Desai Mayur P., Birhade Deekshaputra R., Shinde Mahadev P.: A novel and efficient total synthesis of (±)-physostigmine. Tetrahetron Lett 2009, 50, 2411. <http://dx.doi.org/10.1016/j.tetlet.2009.03.012>
• Sugano Naoki, Koizumi Yuuki, Hirai Go, Oguri Hiroki, Kobayashi Shoji, Yamashita Shuji, Hirama Masahiro: Enantioselective Synthesis of the Fully Functionalized ABC Ring of Zoanthenol. Chem Asian J 2008, 3, 1549. <http://dx.doi.org/10.1002/asia.200800079>
• Majumdar K.C., Chattopadhyay B., Sinha B.: Novel synthesis of oxocine derivatives by Wittig olefination and intramolecular Heck reaction via 8-endo trig cyclization. Tetrahetron Lett 2008, 49, 1319. <http://dx.doi.org/10.1016/j.tetlet.2007.12.096>
• Mohr Justin T., Krout Michael R., Stoltz Brian M.: Natural products as inspiration for the development of asymmetric catalysis. Appl Opt 2008, 455, 323. <http://dx.doi.org/10.1038/nature07370>
• Kantam M. Lakshmi, Kumar K. B. Shiva, Srinivas P., Sreedhar B.: Fluorapatite-Supported Palladium Catalyst for Suzuki and Heck Coupling Reactions of Haloarenes. Adv Synth Catal 2007, 349, 1141. <http://dx.doi.org/10.1002/adsc.200600387>
• Bi Hai-Peng, Liu Xue-Yuan, Gou Fa-Rong, Guo Li-Na, Duan Xin-Hua, Shu Xing-Zhong, Liang Yong-Min: Highly Regioselective Synthesis of Spirocyclic Compounds by a Palladium-Catalyzed Intermolecular Tandem Reaction. Angew Chem 2007, 119, 7198. <http://dx.doi.org/10.1002/ange.200702238>
• Bi Hai-Peng, Liu Xue-Yuan, Gou Fa-Rong, Guo Li-Na, Duan Xin-Hua, Shu Xing-Zhong, Liang Yong-Min: Highly Regioselective Synthesis of Spirocyclic Compounds by a Palladium-Catalyzed Intermolecular Tandem Reaction. Angew Chem Int Ed 2007, 46, 7068. <http://dx.doi.org/10.1002/anie.200702238>
• Nicolaou K. C., Edmonds David J., Bulger Paul G.: Kaskadenreaktionen in der Totalsynthese. Angew Chem 2006, 118, 7292. <http://dx.doi.org/10.1002/ange.200601872>
• Nicolaou K. C., Edmonds David J., Bulger Paul G.: Cascade Reactions in Total Synthesis. Angew Chem Int Ed 2006, 45, 7134. <http://dx.doi.org/10.1002/anie.200601872>
• May Jeremy A., Stoltz Brian: The structural and synthetic implications of the biosynthesis of the calycanthaceous alkaloids, the communesins, and nomofungin. Tetrahedron 2006, 62, 5262. <http://dx.doi.org/10.1016/j.tet.2006.01.105>
• Wang Qiu, Nara Shinji, Padwa Albert: A New Synthesis of γ-Lactams Based on the Reaction of Vinyl Sulfilimines with Dichloroketene. Org Lett 2005, 7, 839. <http://dx.doi.org/10.1021/ol047453j>
• Tobrman Tomáš, Dvořák Dalimil: ‘Reductive Heck reaction’ of 6-halopurines. Tetrahetron Lett 2004, 45, 273. <http://dx.doi.org/10.1016/j.tetlet.2003.10.181>
• Artman Gerald D., Weinreb Steven M.: An Approach to the Total Synthesis of the Marine Ascidian Metabolite Perophoramidine via a Halogen-Selective Tandem Heck/Carbonylation Strategy. Org Lett 2003, 5, 1523. <http://dx.doi.org/10.1021/ol034314d>
• Geng Xudong, Miller Michael L., Lin Songnian, Ojima Iwao: Synthesis of Novel C2−C3‘N-Linked Macrocyclic Taxoids by Means of Highly Regioselective Heck Macrocyclization. Org Lett 2003, 5, 3733. <http://dx.doi.org/10.1021/ol0354627>
• Solabannavar S. B., Helavi V. B., Desai U. V., Mane R. B.: Application of Amberlite IRA-400 (Basic) as a Base in Heck Reaction. Synth Common 2003, 33, 361. <http://dx.doi.org/10.1081/SCC-120015763>
• Jiang S.Anna, Tann Chou-Hong, Thiruvengadam T.K., Zhang Fucheng, Fu Xiaoyong, Zhang Shuyi, Yin Jianguo, McAllister Timothy L.: First examples of a tosylate in the palladium-catalyzed Heck cross coupling reaction. Tetrahetron Lett 2002, 43, 573. <http://dx.doi.org/10.1016/S0040-4039(01)02240-7>
• Harrowven David C., Woodcock Timothy, Howes Peter D.: A tandem Heck reaction leading to a 26-membered carbocycle. Tetrahetron Lett 2002, 43, 9327. <http://dx.doi.org/10.1016/S0040-4039(02)02343-2>
• Hosokawa Takahiro, Kamiike Taisuke, Murahashi Shun-Ichi, Shimada Mamoru, Sugafuji Toshihiro: The Heck reaction in the presence of molecular oxygen. Tetrahetron Lett 2002, 43, 9323. <http://dx.doi.org/10.1016/S0040-4039(02)02372-9>
• Bolm Carsten, Hildebrand Jens P., Muñiz Kilian, Hermanns Nina: Katalysierte asymmetrische Arylierungen. Angew Chem 2001, 113, 3382. <http://dx.doi.org/10.1002/1521-3757(20010917)113:18<3382::AID-ANGE3382>3.0.CO;2-W>
• Böhm Volker P. W., Herrmann Wolfgang A.: Mechanism of the Heck Reaction Using a Phosphapalladacycle as the Catalyst: Classical versus Palladium(IV) Intermediates. Chem Eur J 2001, 7, 4191. <http://dx.doi.org/10.1002/1521-3765(20011001)7:19<4191::AID-CHEM4191>3.0.CO;2-1>
• Bolm Carsten, Hildebrand Jens P., Muñiz Kilian, Hermanns Nina: Catalyzed Asymmetric Arylation Reactions. Angew Chem Int Ed 2001, 40, 3284. <http://dx.doi.org/10.1002/1521-3773(20010917)40:18<3284::AID-ANIE3284>3.0.CO;2-U>
• Gilbertson Scott R, Fu Zice, Xie Dejian: Proline derived phosphine–oxazoline ligands in the asymmetric Heck reaction. Tetrahetron Lett 2001, 42, 365. <http://dx.doi.org/10.1016/S0040-4039(00)01938-9>
• Hirai Go, Oguri Hiroki, Moharram Sameh M, Koyama Koji, Hirama Masahiro: Convergent synthesis of the ABC-ring moiety of zoanthenol: intramolecular Mizoroki–Heck reaction. Tetrahetron Lett 2001, 42, 5783. <http://dx.doi.org/10.1016/S0040-4039(01)01110-8>
• Kiewel Kurt, Tallant Mathew, Sulikowski Gary A: Asymmetric Heck cyclization route to indolizidine and azaazulene alkaloids: synthesis of (+)-5-epiindolizidine 167B and indolizidine 223AB. Tetrahetron Lett 2001, 42, 6621. <http://dx.doi.org/10.1016/S0040-4039(01)01361-2>
• Cao Ping, Zhang Xumu: The First Highly Enantioselective Rh-Catalyzed Enyne Cycloisomerization. Angew Chem 2000, 112, 4270. <http://dx.doi.org/10.1002/1521-3757(20001117)112:22<4270::AID-ANGE4270>3.0.CO;2-8>
• Cao Ping, Zhang Xumu: The First Highly Enantioselective Rh-Catalyzed Enyne Cycloisomerization. Angew Chem 2000, 39, 4104. <http://dx.doi.org/10.1002/1521-3773(20001117)39:22<4104::AID-ANIE4104>3.0.CO;2-X>
• Frackenpohl Jens: Morphin und Opioid-Analgetika. Chem Unserer Zeit 2000, 34, 99. <http://dx.doi.org/10.1002/1521-3781(200004)34:2<99::AID-CIUZ99>3.0.CO;2-X>
• Oh Chang Ho, Jung Hyung Hoon, Kim Joo Sung, Cho Seung Woo: Highly Regio- and Stereoselective Cycloreductions of 1,6- and 1,7-Enynes Activated with a Carbonyl Functionality. Angew Chem 2000, 112, 768. <http://dx.doi.org/10.1002/(SICI)1521-3757(20000218)112:4<768::AID-ANGE768>3.0.CO;2-K>
• Shibasaki M, Vogl E.M: The palladium-catalysed arylation and vinylation of alkenes—enantioselective fashion. J Organomet Chem 1999, 576, 1. <http://dx.doi.org/10.1016/S0022-328X(98)01048-1>
• Liu Bing, Padwa Albert: A new and convenient synthesis of 2-amidofurans using the Jacobi bis-heteroannulation method. Tetrahetron Lett 1999, 40, 1645. <http://dx.doi.org/10.1016/S0040-4039(99)00071-4>
• Bräse Stefan, Rümper Jörg, Voigt Katharina, Albecq Stephane, Thurau Gert, Villard Renaud, Waegell Bernard, de Meijere Armin: Synthesis ofo-Dialkenylbenzenes and Indenes Using Heck and Oxypalladation Reactions. Eur J Org Chem 1998, 1998, 671. <http://dx.doi.org/10.1002/(SICI)1099-0690(199804)1998:4<671::AID-EJOC671>3.0.CO;2-R>
• Corey E. J., Guzman-Perez Angel: Der katalytische enantioselektive Aufbau von Molekülen mit quartären Kohlenstoff-Stereozentren. Angew Chem 1998, 110, 402. <http://dx.doi.org/10.1002/(SICI)1521-3757(19980216)110:4<402::AID-ANGE402>3.0.CO;2-6>
• Diaz Philippe, Gendre Fabrice, Stella Lucien, Charpentier Bruno: New synthetic retinoids obtained by palladium-catalyzed tandem cyclisation-hydride capture process. Tetrahedron 1998, 54, 4579. <http://dx.doi.org/10.1016/S0040-4020(98)00169-0>
• Takacs James M., Jaber Mohamad R., Strakhov Alexander V., Athalye Rajan V.: Palladium-catalyzed bisdiene carboxyclizations: cycloisomerizations of bisdienes bearing an ester substituent. Tetrahetron Lett 1998, 39, 5003. <http://dx.doi.org/10.1016/S0040-4039(98)00979-4>
• T. Crisp Geoffrey: Variations on a theme—recent developments on the mechanism of the Heck reaction and their implications for synthesis. Chem Soc Rev 1998, 27, 427. <http://dx.doi.org/10.1039/a827427z>
• Shibasaki Masakatsu, Boden Christopher D.J., Kojima Akihiko: The asymmetric Heck reaction. Tetrahedron 1997, 53, 7371. <http://dx.doi.org/10.1016/S0040-4020(97)00437-7>
• Cheng Chen-Yu, Liou Jing-Ping, Lee Mei-Jing: Synthesis of morphine fragments spiro[benzofuran-3(2H),4′-piperidine] and octahydro-1H-benzofuro[3,2-e]isoquinoline by intramolecular Heck reaction. Tetrahetron Lett 1997, 38, 4571. <http://dx.doi.org/10.1016/S0040-4039(97)00976-3>
• Wang Zhong, Lu Xiyan: Palladium-catalyzed intramolecular alkyne-α,β-unsaturated carbonyl coupling. A formal synthesis of (+)-pilocarpine. Tetrahetron Lett 1997, 38, 5213. <http://dx.doi.org/10.1016/S0040-4039(97)01114-3>
• Loiseleur Olivier, Meier Peter, Pfaltz Andreas: Chirale Phosphanyldihydrooxazole in der asymmetrischen Katalyse: enantioselektive Heck-Reaktionen. Angew Chem 1996, 108, 218. <http://dx.doi.org/10.1002/ange.19961080223>
• Beller Matthias, Riermeier Thomas H., Haber Steffen, Kleiner Hans-Jerg, Herrmann Wolfgang A.: Palladium-Catalyzed Reactions in Industry, 4[]. Synthesis of New Palladium Catalysts: First Isolation and Characterization of all Intermediates in a Cyclopalladation Reaction. Chem Ber 1996, 129, 1259. <http://dx.doi.org/10.1002/cber.19961291018>
• Hegedus Louis S.: Transition metals in organic synthesis highlights for the year 1994. Coord Chem Rev - 1996, 147, 443. <http://dx.doi.org/10.1016/0010-8545(95)00000-3>
• Heumann Andreas, Réglier Marius: The stereochemistry of palladium catalysed cyclisation reactions part C: Cascade reactions. Tetrahedron 1996, 52, 9289. <http://dx.doi.org/10.1016/0040-4020(96)00545-5>
• Grigg Ronald, Putnikovic Bogdan, Urch Christopher J: Palladium catalysed ter- and tetra-molecular queuing processes. One-pot routes to 3-spiro-2-oxindoles and 3-spiro-2(3H)-benzofuranones. Tetrahetron Lett 1996, 37, 695. <http://dx.doi.org/10.1016/0040-4039(95)02245-7>
• Moinet Christophe, Fiaud Jean-Claude: Palladium-catalyzed asymmetric hydrophenylation of 1,4-dihydro-1,4-epoxynaphthalene. Tetrahetron Lett 1995, 36, 2051. <http://dx.doi.org/10.1016/0040-4039(95)00178-F>
• Sugihara Takumichi, Takebayashi Masahiro, Kaneko Chikara: Effects of high pressure on the heck reaction. Is it possible to control dehydropalladation of alkylpalladium intermediates having β-hydrogens?. Tetrahetron Lett 1995, 36, 5547. <http://dx.doi.org/10.1016/0040-4039(95)01048-M>
• Wünsch Bernhard, Diekmann Heike, Höfner Georg: Stereoselective synthesis of 2-aminoethyl substituted tricycles with NMDA receptor affinity. Tet Asymm 1995, 6, 1527. <http://dx.doi.org/10.1016/0957-4166(95)00190-Z>
• Murai Toshiaki, Takada Hiroya, Kanda Takahiro, Kato Shinzi: Selective Allylations of Selenothioic Acid S-Alkyl Esters with Allylic Bromides. Chem Lett 1995, 1057. <http://dx.doi.org/10.1246/cl.1995.1057>
• De Meijere Armin, Meyer Frank E.: Kleider machen Leute: Heck-Reaktion im neuen Gewand. Angew Chem 1994, 106, 2473. <http://dx.doi.org/10.1002/ange.19941062307>