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Negišiovo párování (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Negišiovo párování" in Czech language version.

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49doi.org
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30nih.gov
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18worldcat.org
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5acs.org
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1zenodo.org
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acs.org

pubs.acs.org

  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. (anglicky) 
  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. 
  • FISCHER, Christian; FU, Gregory C. Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents. Journal of the American Chemical Society. April 2005, s. 4594–4595. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0506509. PMID 15796523. 
  • SON, Sunghee; FU, Gregory C. Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs. Journal of the American Chemical Society. 2008-03-01, s. 2756–2757. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja800103z. PMID 18257579. 
  • SASE, Shohei; JARIC, Milica; METZGER, Albrecht; MALAKHOV, Vladimir; KNOCHEL, Paul. One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates. The Journal of Organic Chemistry. 2008-09-19, s. 7380–7382. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo801063c. PMID 18693766. 

doi.org

dx.doi.org

  • KING, Anthony O.; OKUKADO, Nobuhisa; NEGISHI, Ei-ichi. Highly general stereo-, regio-, and chemo-selective synthesis of terminal and internal conjugated enynes by the Pd-catalysed reaction of alkynylzinc reagents with alkenyl halides. Journal of the Chemical Society, Chemical Communications. 1977, s. 683. DOI 10.1039/C39770000683. 
  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. (anglicky) 
  • NEGISHI, Eiichi; KING, Anthony O.; OKUKADO, Nobuhisa. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides. The Journal of Organic Chemistry. 1977-05-01, s. 1821–1823. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo00430a041. 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • Baba S, Negishi E. A novel stereospecific alkenyl-alkenyl cross-coupling by a palladium- or nickel-catalyzed reaction of alkenylalanes with alkenyl halides. Journal of the American Chemical Society. 1976, s. 6729–6731. DOI 10.1021/ja00437a067. 
  • Negishi E., King A. O., Okukado N. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides. The Journal of Organic Chemistry. 1977, s. 1821–1823. DOI 10.1021/jo00430a041. 
  • Casado AL, Espinet P. On the Configuration Resulting from Oxidative Addition of RX to Pd(PPh3)4 and the Mechanism of the cis-to-trans Isomerization of [PdRX(PPh3)2] Complexes (R = Aryl, X = Halide). Organometallics. 1998, s. 954–959. DOI 10.1021/om9709502. 
  • McCann LC, Hunter HN, Clyburne JA, Organ MG. Higher-order zincates as transmetalators in alkyl-alkyl negishi cross-coupling. Angewandte Chemie. July 2012, s. 7024–7. DOI 10.1002/anie.201203547. PMID 22685029. 
  • García-Melchor M., Braga A. A., Lledós A., Ujaque G., Maseras F. Computational perspective on Pd-catalyzed C-C cross-coupling reaction mechanisms. Accounts of Chemical Research. November 2013, s. 2626–34. DOI 10.1021/ar400080r. PMID 23848308. 
  • Casares J. A., Espinet P., Fuentes B., Salas G. Insights into the mechanism of the Negishi reaction: ZnRX versus ZnR2 reagents. Journal of the American Chemical Society. March 2007, s. 3508–9. DOI 10.1021/ja070235b. PMID 17328551. 
  • Fuentes B., García-Melchor M., Lledós A., Maseras F., Casares J. A., Ujaque G., Espinet P. Palladium round trip in the Negishi coupling of trans-[PdMeCl(PMePh2)2] with ZnMeCl: an experimental and DFT study of the transmetalation step. Chemistry. August 2010, s. 8596–9. DOI 10.1002/chem.201001332. PMID 20623568. 
  • Liu Q, Lan Y, Liu J, Li G, Wu Y. D., Lei A. Revealing a second transmetalation step in the Negishi coupling and its competition with reductive elimination: improvement in the interpretation of the mechanism of biaryl syntheses. Journal of the American Chemical Society. July 2009, s. 10201–10. DOI 10.1021/ja903277d. PMID 19572717. 
  • PHAPALE, Vilas B.; CÁRDENAS, Diego J. Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms. Chemical Society Reviews. 2009-05-27, s. 1598–1607. Dostupné online. ISSN 1460-4744. DOI 10.1039/B805648J. PMID 19587955. 
  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. 
  • SCHLEY, Nathan D.; FU, Gregory C. Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation. Journal of the American Chemical Society. 2014-11-26, s. 16588–16593. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja508718m. PMID 25402209. 
  • MORRELL, Dennis G.; KOCHI, Jay K. Mechanistic studies of nickel catalysis in the cross coupling of aryl halides with alkylmetals. Role of arylalkylnickel(II) species as intermediates. Journal of the American Chemical Society. 1975-12-01, s. 7262–7270. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja00858a011. 
  • Yu Y., Bond A. D., Leonard P. W., Lorenz U. J., Timofeeva T. V., Vollhardt K. P., Whitener G. D., Yakovenko A. A. Hexaferrocenylbenzene. Chemical Communications. June 2006, s. 2572–4. Dostupné online. DOI 10.1039/b604844g. PMID 16779481. 
  • Zhao Y., Wang H., Hou X., Hu Y., Lei A., Zhang H., Zhu L. Oxidative cross-coupling through double transmetallation: surprisingly high selectivity for palladium-catalyzed cross-coupling of alkylzinc and alkynylstannanes. Journal of the American Chemical Society. November 2006, s. 15048–9. DOI 10.1021/ja0647351. PMID 17117830. 
  • Yang Y., Oldenhuis N. J., Buchwald S. L. Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts. Angewandte Chemie. January 2013, s. 615–9. DOI 10.1002/anie.201207750. PMID 23172689. 
  • NEGISHI, Eiichi; KING, Anthony O.; OKUKADO, Nobuhisa. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides. The Journal of Organic Chemistry. 1977-05-01, s. 1821–1823. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo00430a041. 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • GIOVANNINI, Riccardo; STÜDEMANN, Thomas; DUSSIN, Gaelle; KNOCHEL, Paul. An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers. Angewandte Chemie International Edition. 1998, s. 2387–2390. Dostupné online. ISSN 1521-3773. DOI 10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M. PMID 29710957. 
  • JENSEN, Anne Eeg; KNOCHEL, Paul. Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides. The Journal of Organic Chemistry. 2002-01-01, s. 79–85. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo0105787. PMID 11777442. 
  • GIOVANNINI, Riccardo; KNOCHEL, Paul. Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides. Journal of the American Chemical Society. 1998-11-01, s. 11186–11187. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja982520o. 
  • FISCHER, Christian; FU, Gregory C. Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents. Journal of the American Chemical Society. April 2005, s. 4594–4595. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0506509. PMID 15796523. 
  • SON, Sunghee; FU, Gregory C. Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs. Journal of the American Chemical Society. 2008-03-01, s. 2756–2757. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja800103z. PMID 18257579. 
  • PHAPALE, Vilas B.; BUÑUEL, Elena; GARCÍA-IGLESIAS, Miguel; CÁRDENAS, Diego J. Ni-Catalyzed Cascade Formation of C(sp3)–C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides. Angewandte Chemie International Edition. 2007, s. 8790–8795. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.200702528. PMID 17918274. 
  • Johansson Seechurn C. C., Kitching M. O., Colacot T. J., Snieckus V. Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize. Angewandte Chemie. May 2012, s. 5062–85. DOI 10.1002/anie.201107017. PMID 22573393. 
  • Sase S., Jaric M., Metzger A., Malakhov V., Knochel P. One-pot Negishi cross-coupling reactions of in situ generated zinc reagents with aryl chlorides, bromides, and triflates. The Journal of Organic Chemistry. September 2008, s. 7380–2. DOI 10.1021/jo801063c. PMID 18693766. 
  • Manley PW, Acemoglu M, Marterer W, Pachinger W. Large-Scale Negishi Coupling as Applied to the Synthesis of PDE472, an Inhibitor of Phosphodiesterase Type 4D. Organic Process Research & Development. 2003, s. 436–445. DOI 10.1021/op025615q. 
  • Torborg C, Beller M. Recent Applications of Palladium-Catalyzed Coupling Reactions in the Pharmaceutical, Agrochemical, and Fine Chemical Industries. Advanced Synthesis & Catalysis. 2009, s. 3027–3043. DOI 10.1002/adsc.200900587. 
  • Nicolaou K. C., Bulger P. G., Sarlah D. Palladium-catalyzed cross-coupling reactions in total synthesis. Angewandte Chemie. July 2005, s. 4442–89. DOI 10.1002/anie.200500368. PMID 15991198. 
  • Lessene G. Advances in the Negishi coupling. Australian Journal of Chemistry. 2004, s. 107. DOI 10.1071/ch03225. 
  • Torssell S., Wanngren E., Somfai P. Total synthesis of (-)-stemoamide. The Journal of Organic Chemistry. May 2007, s. 4246–9. DOI 10.1021/jo070498o. PMID 17451274. 
  • Aoyagi S., Hirashima S., Saito K., Kibayashi C. Convergent Approach to Pumiliotoxin Alkaloids. Asymmetric Total Synthesis of (+)-Pumiliotoxins A, B, and 225F. The Journal of Organic Chemistry. 2002, s. 5517–5526. DOI 10.1021/jo0200466. PMID 12153249. 
  • Maloney DJ, Hecht SM. A stereocontrolled synthesis of delta-trans-tocotrienoloic acid. Organic Letters. September 2005, s. 4297–300. DOI 10.1021/ol051849t. PMID 16146411. 
  • SMITH, Sean W.; FU, Gregory C. Nickel-Catalyzed Negishi Cross-Couplings of Secondary Nucleophiles with Secondary Propargylic Electrophiles at Room Temperature. Angewandte Chemie International Edition. 2008, s. 9334–9336. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.200802784. PMID 18972493. 
  • SCHMIDT, Thomas; KIRSCHNING, Andreas. Total Synthesis of Carolacton, a Highly Potent Biofilm Inhibitor. Angewandte Chemie International Edition. 2012, s. 1063–1066. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.201106762. PMID 22162345. 
  • Huo S. Highly efficient, general procedure for the preparation of alkylzinc reagents from unactivated alkyl bromides and chlorides. Organic Letters. February 2003, s. 423–5. DOI 10.1021/ol0272693. PMID 12583734. 
  • Giovannini R., Knochel P. Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides. Journal of the American Chemical Society. 1998, s. 11186–11187. DOI 10.1021/ja982520o. 
  • SASE, Shohei; JARIC, Milica; METZGER, Albrecht; MALAKHOV, Vladimir; KNOCHEL, Paul. One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates. The Journal of Organic Chemistry. 2008-09-19, s. 7380–7382. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo801063c. PMID 18693766. 

doi.org

  • NEGISHI, Eiichi; KING, Anthony O.; OKUKADO, Nobuhisa. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides. The Journal of Organic Chemistry. 1977-05-01, s. 1821–1823. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo00430a041. 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • SCHLEY, Nathan D.; FU, Gregory C. Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation. Journal of the American Chemical Society. 2014-11-26, s. 16588–16593. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja508718m. PMID 25402209. 
  • MORRELL, Dennis G.; KOCHI, Jay K. Mechanistic studies of nickel catalysis in the cross coupling of aryl halides with alkylmetals. Role of arylalkylnickel(II) species as intermediates. Journal of the American Chemical Society. 1975-12-01, s. 7262–7270. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja00858a011. 
  • NEGISHI, Eiichi; KING, Anthony O.; OKUKADO, Nobuhisa. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides. The Journal of Organic Chemistry. 1977-05-01, s. 1821–1823. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo00430a041. 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • JENSEN, Anne Eeg; KNOCHEL, Paul. Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides. The Journal of Organic Chemistry. 2002-01-01, s. 79–85. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo0105787. PMID 11777442. 
  • GIOVANNINI, Riccardo; KNOCHEL, Paul. Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides. Journal of the American Chemical Society. 1998-11-01, s. 11186–11187. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja982520o. 

nih.gov

ncbi.nlm.nih.gov

  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. (anglicky) 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • McCann LC, Hunter HN, Clyburne JA, Organ MG. Higher-order zincates as transmetalators in alkyl-alkyl negishi cross-coupling. Angewandte Chemie. July 2012, s. 7024–7. DOI 10.1002/anie.201203547. PMID 22685029. 
  • García-Melchor M., Braga A. A., Lledós A., Ujaque G., Maseras F. Computational perspective on Pd-catalyzed C-C cross-coupling reaction mechanisms. Accounts of Chemical Research. November 2013, s. 2626–34. DOI 10.1021/ar400080r. PMID 23848308. 
  • Casares J. A., Espinet P., Fuentes B., Salas G. Insights into the mechanism of the Negishi reaction: ZnRX versus ZnR2 reagents. Journal of the American Chemical Society. March 2007, s. 3508–9. DOI 10.1021/ja070235b. PMID 17328551. 
  • Fuentes B., García-Melchor M., Lledós A., Maseras F., Casares J. A., Ujaque G., Espinet P. Palladium round trip in the Negishi coupling of trans-[PdMeCl(PMePh2)2] with ZnMeCl: an experimental and DFT study of the transmetalation step. Chemistry. August 2010, s. 8596–9. DOI 10.1002/chem.201001332. PMID 20623568. 
  • Liu Q, Lan Y, Liu J, Li G, Wu Y. D., Lei A. Revealing a second transmetalation step in the Negishi coupling and its competition with reductive elimination: improvement in the interpretation of the mechanism of biaryl syntheses. Journal of the American Chemical Society. July 2009, s. 10201–10. DOI 10.1021/ja903277d. PMID 19572717. 
  • PHAPALE, Vilas B.; CÁRDENAS, Diego J. Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms. Chemical Society Reviews. 2009-05-27, s. 1598–1607. Dostupné online. ISSN 1460-4744. DOI 10.1039/B805648J. PMID 19587955. 
  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. 
  • SCHLEY, Nathan D.; FU, Gregory C. Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation. Journal of the American Chemical Society. 2014-11-26, s. 16588–16593. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja508718m. PMID 25402209. 
  • Yu Y., Bond A. D., Leonard P. W., Lorenz U. J., Timofeeva T. V., Vollhardt K. P., Whitener G. D., Yakovenko A. A. Hexaferrocenylbenzene. Chemical Communications. June 2006, s. 2572–4. Dostupné online. DOI 10.1039/b604844g. PMID 16779481. 
  • Zhao Y., Wang H., Hou X., Hu Y., Lei A., Zhang H., Zhu L. Oxidative cross-coupling through double transmetallation: surprisingly high selectivity for palladium-catalyzed cross-coupling of alkylzinc and alkynylstannanes. Journal of the American Chemical Society. November 2006, s. 15048–9. DOI 10.1021/ja0647351. PMID 17117830. 
  • Yang Y., Oldenhuis N. J., Buchwald S. L. Mild and general conditions for negishi cross-coupling enabled by the use of palladacycle precatalysts. Angewandte Chemie. January 2013, s. 615–9. DOI 10.1002/anie.201207750. PMID 23172689. 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • GIOVANNINI, Riccardo; STÜDEMANN, Thomas; DUSSIN, Gaelle; KNOCHEL, Paul. An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers. Angewandte Chemie International Edition. 1998, s. 2387–2390. Dostupné online. ISSN 1521-3773. DOI 10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M. PMID 29710957. 
  • JENSEN, Anne Eeg; KNOCHEL, Paul. Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides. The Journal of Organic Chemistry. 2002-01-01, s. 79–85. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo0105787. PMID 11777442. 
  • FISCHER, Christian; FU, Gregory C. Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents. Journal of the American Chemical Society. April 2005, s. 4594–4595. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0506509. PMID 15796523. 
  • SON, Sunghee; FU, Gregory C. Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs. Journal of the American Chemical Society. 2008-03-01, s. 2756–2757. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja800103z. PMID 18257579. 
  • PHAPALE, Vilas B.; BUÑUEL, Elena; GARCÍA-IGLESIAS, Miguel; CÁRDENAS, Diego J. Ni-Catalyzed Cascade Formation of C(sp3)–C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides. Angewandte Chemie International Edition. 2007, s. 8790–8795. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.200702528. PMID 17918274. 
  • Johansson Seechurn C. C., Kitching M. O., Colacot T. J., Snieckus V. Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize. Angewandte Chemie. May 2012, s. 5062–85. DOI 10.1002/anie.201107017. PMID 22573393. 
  • Sase S., Jaric M., Metzger A., Malakhov V., Knochel P. One-pot Negishi cross-coupling reactions of in situ generated zinc reagents with aryl chlorides, bromides, and triflates. The Journal of Organic Chemistry. September 2008, s. 7380–2. DOI 10.1021/jo801063c. PMID 18693766. 
  • Nicolaou K. C., Bulger P. G., Sarlah D. Palladium-catalyzed cross-coupling reactions in total synthesis. Angewandte Chemie. July 2005, s. 4442–89. DOI 10.1002/anie.200500368. PMID 15991198. 
  • Torssell S., Wanngren E., Somfai P. Total synthesis of (-)-stemoamide. The Journal of Organic Chemistry. May 2007, s. 4246–9. DOI 10.1021/jo070498o. PMID 17451274. 
  • Gusovsky F., Padgett W. L., Creveling C. R., Daly J. W. Interaction of pumiliotoxin B with an "alkaloid-binding domain" on the voltage-dependent sodium channel. Molecular Pharmacology. December 1992, s. 1104–8. PMID 1336116. 
  • Aoyagi S., Hirashima S., Saito K., Kibayashi C. Convergent Approach to Pumiliotoxin Alkaloids. Asymmetric Total Synthesis of (+)-Pumiliotoxins A, B, and 225F. The Journal of Organic Chemistry. 2002, s. 5517–5526. DOI 10.1021/jo0200466. PMID 12153249. 
  • Maloney DJ, Hecht SM. A stereocontrolled synthesis of delta-trans-tocotrienoloic acid. Organic Letters. September 2005, s. 4297–300. DOI 10.1021/ol051849t. PMID 16146411. 
  • SMITH, Sean W.; FU, Gregory C. Nickel-Catalyzed Negishi Cross-Couplings of Secondary Nucleophiles with Secondary Propargylic Electrophiles at Room Temperature. Angewandte Chemie International Edition. 2008, s. 9334–9336. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.200802784. PMID 18972493. 
  • SCHMIDT, Thomas; KIRSCHNING, Andreas. Total Synthesis of Carolacton, a Highly Potent Biofilm Inhibitor. Angewandte Chemie International Edition. 2012, s. 1063–1066. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.201106762. PMID 22162345. 
  • Huo S. Highly efficient, general procedure for the preparation of alkylzinc reagents from unactivated alkyl bromides and chlorides. Organic Letters. February 2003, s. 423–5. DOI 10.1021/ol0272693. PMID 12583734. 
  • SASE, Shohei; JARIC, Milica; METZGER, Albrecht; MALAKHOV, Vladimir; KNOCHEL, Paul. One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates. The Journal of Organic Chemistry. 2008-09-19, s. 7380–7382. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo801063c. PMID 18693766. 

orgsyn.org

  • ADAM P. SMITH, SCOTT A. SAVAGE, J. CHRISTOPHER LOVE, AND CASSANDRA L. FRASER. Synthesis of 4-, 5-, and 6-methyl-2,2'-bipyridine by a Negishi cross-coupling strategy: 5-methyl-2,2'-bipyridine. Org. Synth.. 2004. Dostupné online. ; Coll. Vol.. S. 517. 
  • EI-ICHI NEGISHI, TAMOTSU TAKAHASHI AND ANTHONY O. KING. Synthesis of biaryls via palladium-catalyzed cross-coupling: 2-methyl-4'-nitrobiphenyl. Org. Synth.. 1993. Dostupné online. ; Coll. Vol.. S. 430. 
  • EI-ICHI NEGISHI, TAMOTSU TAKAHASHI, AND SHIGERU BABA. Palladium-catalyzed synthesis of conjugated dienes. Org. Synth.. 1993. Dostupné online. ; Coll. Vol.. S. 295. 

rsc.org

pubs.rsc.org

web.archive.org

  • Andrew G Myers Research Group. Chemistry 115 Handouts [online]. Boston: Harvard University Department of Chemistry [cit. 2021-11-02]. Dostupné v archivu pořízeném dne 2019-03-29. 

wiley.com

onlinelibrary.wiley.com

worldcat.org

  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. (anglicky) 
  • NEGISHI, Eiichi; KING, Anthony O.; OKUKADO, Nobuhisa. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides. The Journal of Organic Chemistry. 1977-05-01, s. 1821–1823. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo00430a041. 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • PHAPALE, Vilas B.; CÁRDENAS, Diego J. Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms. Chemical Society Reviews. 2009-05-27, s. 1598–1607. Dostupné online. ISSN 1460-4744. DOI 10.1039/B805648J. PMID 19587955. 
  • ZHOU, Jianrong (Steve); FU, Gregory C. Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides. Journal of the American Chemical Society. December 2003, s. 14726–14727. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0389366. PMID 14640646. 
  • SCHLEY, Nathan D.; FU, Gregory C. Nickel-Catalyzed Negishi Arylations of Propargylic Bromides: A Mechanistic Investigation. Journal of the American Chemical Society. 2014-11-26, s. 16588–16593. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja508718m. PMID 25402209. 
  • MORRELL, Dennis G.; KOCHI, Jay K. Mechanistic studies of nickel catalysis in the cross coupling of aryl halides with alkylmetals. Role of arylalkylnickel(II) species as intermediates. Journal of the American Chemical Society. 1975-12-01, s. 7262–7270. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja00858a011. 
  • NEGISHI, Eiichi; KING, Anthony O.; OKUKADO, Nobuhisa. Selective carbon-carbon bond formation via transition metal catalysis. 3. A highly selective synthesis of unsymmetrical biaryls and diarylmethanes by the nickel- or palladium-catalyzed reaction of aryl- and benzylzinc derivatives with aryl halides. The Journal of Organic Chemistry. 1977-05-01, s. 1821–1823. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo00430a041. 
  • GAVRYUSHIN, Andrei; KOFINK, Christiane; MANOLIKAKES, Georg; KNOCHEL, Paul. Efficient Cross-Coupling of Functionalized Arylzinc Halides Catalyzed by a Nickel Chloride−Diethyl Phosphite System. Organic Letters. 2005-10-01, s. 4871–4874. Dostupné online. ISSN 1523-7060. DOI 10.1021/ol051615+. PMID 16235910. 
  • GIOVANNINI, Riccardo; STÜDEMANN, Thomas; DUSSIN, Gaelle; KNOCHEL, Paul. An Efficient Nickel-Catalyzed Cross-Coupling Between sp3 Carbon Centers. Angewandte Chemie International Edition. 1998, s. 2387–2390. Dostupné online. ISSN 1521-3773. DOI 10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO;2-M. PMID 29710957. 
  • JENSEN, Anne Eeg; KNOCHEL, Paul. Nickel-Catalyzed Cross-Coupling between Functionalized Primary or Secondary Alkylzinc Halides and Primary Alkyl Halides. The Journal of Organic Chemistry. 2002-01-01, s. 79–85. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo0105787. PMID 11777442. 
  • GIOVANNINI, Riccardo; KNOCHEL, Paul. Ni(II)-Catalyzed Cross-Coupling between Polyfunctional Arylzinc Derivatives and Primary Alkyl Iodides. Journal of the American Chemical Society. 1998-11-01, s. 11186–11187. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja982520o. 
  • FISCHER, Christian; FU, Gregory C. Asymmetric Nickel-Catalyzed Negishi Cross-Couplings of Secondary α-Bromo Amides with Organozinc Reagents. Journal of the American Chemical Society. April 2005, s. 4594–4595. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja0506509. PMID 15796523. 
  • SON, Sunghee; FU, Gregory C. Nickel-Catalyzed Asymmetric Negishi Cross-Couplings of Secondary Allylic Chlorides with Alkylzincs. Journal of the American Chemical Society. 2008-03-01, s. 2756–2757. Dostupné online. ISSN 0002-7863. DOI 10.1021/ja800103z. PMID 18257579. 
  • PHAPALE, Vilas B.; BUÑUEL, Elena; GARCÍA-IGLESIAS, Miguel; CÁRDENAS, Diego J. Ni-Catalyzed Cascade Formation of C(sp3)–C(sp3) Bonds by Cyclization and Cross-Coupling Reactions of Iodoalkanes with Alkyl Zinc Halides. Angewandte Chemie International Edition. 2007, s. 8790–8795. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.200702528. PMID 17918274. 
  • SMITH, Sean W.; FU, Gregory C. Nickel-Catalyzed Negishi Cross-Couplings of Secondary Nucleophiles with Secondary Propargylic Electrophiles at Room Temperature. Angewandte Chemie International Edition. 2008, s. 9334–9336. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.200802784. PMID 18972493. 
  • SCHMIDT, Thomas; KIRSCHNING, Andreas. Total Synthesis of Carolacton, a Highly Potent Biofilm Inhibitor. Angewandte Chemie International Edition. 2012, s. 1063–1066. Dostupné online. ISSN 1521-3773. DOI 10.1002/anie.201106762. PMID 22162345. 
  • SASE, Shohei; JARIC, Milica; METZGER, Albrecht; MALAKHOV, Vladimir; KNOCHEL, Paul. One-Pot Negishi Cross-Coupling Reactions of In Situ Generated Zinc Reagents with Aryl Chlorides, Bromides, and Triflates. The Journal of Organic Chemistry. 2008-09-19, s. 7380–7382. Dostupné online. ISSN 0022-3263. DOI 10.1021/jo801063c. PMID 18693766. 

zenodo.org

  • Yu Y., Bond A. D., Leonard P. W., Lorenz U. J., Timofeeva T. V., Vollhardt K. P., Whitener G. D., Yakovenko A. A. Hexaferrocenylbenzene. Chemical Communications. June 2006, s. 2572–4. Dostupné online. DOI 10.1039/b604844g. PMID 16779481.